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Volumn 62, Issue 10, 1997, Pages 3370-3374

Cyclopropanation with Diazomethane and Bis(oxazoline)palladium(II) Complexes

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Indexed keywords


EID: 1542398427     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo970044z     Document Type: Article
Times cited : (29)

References (161)
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    • (1995) Comprehensive Organometallic Chemistry II , vol.12
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    • For reviews see (b) Pfaltz, A. Chimia 1990, 44, 202. (c) Bolm, C. Angew. Chem., Int. Ed. Engl. 1991, 30, 542. (d) Pfaltz, A. Acc. Chem. Res. 1993, 26, 339.
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    • For reviews see (b) Pfaltz, A. Chimia 1990, 44, 202. (c) Bolm, C. Angew. Chem., Int. Ed. Engl. 1991, 30, 542. (d) Pfaltz, A. Acc. Chem. Res. 1993, 26, 339.
    • (1991) Angew. Chem., Int. Ed. Engl. , vol.30 , pp. 542
    • Bolm, C.1
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    • For reviews see (b) Pfaltz, A. Chimia 1990, 44, 202. (c) Bolm, C. Angew. Chem., Int. Ed. Engl. 1991, 30, 542. (d) Pfaltz, A. Acc. Chem. Res. 1993, 26, 339.
    • (1993) Acc. Chem. Res. , vol.26 , pp. 339
    • Pfaltz, A.1
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    • 84987263015 scopus 로고
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1995) Helv. Chim. Acta , vol.78 , pp. 265
    • Von Matt, P.1    Lloyd-Jones, G.C.2    Minidis, A.B.E.3    Pfaltz, A.4    Macko, L.5    Neuburger, M.6    Zehnder, M.7    Rüegger, H.8    Pregosin, P.S.9
  • 17
    • 0026588815 scopus 로고
    • Allylic oxidation
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1992) Tetrahedron , vol.48 , pp. 2143
    • Leutenegger, U.1    Umbricht, G.2    Fahrni, C.3    Von Matt, P.4    Pfaltz, A.5
  • 18
    • 0028944316 scopus 로고
    • Hydrosilylation
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 1831
    • Gokhale, A.S.1    Minidis, A.B.E.2    Pfaltz, A.3
  • 19
    • 0000876890 scopus 로고
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1993) Chem. Lett. , pp. 347
    • Nagashima, H.1    Ueda, T.2    Nishiyama, H.3    Itoh, K.4
  • 20
    • 0027409440 scopus 로고
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1993) Tetrahedron Asymm. , vol.4 , pp. 143
    • Nishiyama, H.1    Yamaguchi, S.2    Park, S.-B.3    Itoh, K.4
  • 21
    • 0000513053 scopus 로고
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1992) J. Org. Chem. , vol.57 , pp. 4306
    • Nishiyama, H.1    Yamaguchi, S.2    Kondo, M.3    Itoh, K.4
  • 22
    • 0000487271 scopus 로고
    • Organometallic additions
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1989) Organometallics , vol.8 , pp. 846
    • Nishiyama, H.1    Sakaguchi, H.2    Nakamura, T.3    Horihata, M.4    Kondo, M.5    Itoh, K.6
  • 23
    • 0000034072 scopus 로고
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 8797
    • Denmark, S.E.1    Nakajima, N.2    Nicaise, O.J.-C.3
  • 24
    • 0002569664 scopus 로고    scopus 로고
    • [4 + 2] Cycloadditions
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1996) Chem. Commun. , pp. 999
    • Denmark, S.E.1    Nicaise, O.J.-C.2
  • 25
    • 33748726159 scopus 로고
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 798
    • Evans, D.A.1    Murry, J.A.2    Von Matt, P.3    Norcross, R.D.4    Miller, S.J.5
  • 26
    • 0342740235 scopus 로고
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1993) J. Am Chem. Soc. , vol.115 , pp. 6460
    • Evans, D.A.1    Miller, S.J.2    Lectka, T.3
  • 27
    • 0027319440 scopus 로고
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 4001
    • Corey, E.J.1    Wang, Z.2
  • 28
    • 0026452321 scopus 로고
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 6807
    • Corey, E.J.1    Ishihara, K.2
  • 29
    • 85022460851 scopus 로고
    • Aziridination
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 728
    • Corey, E.J.1    Imai, N.2    Zhang, H.-Y.3
  • 30
    • 33748236032 scopus 로고
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 676
    • Hansen, K.B.1    Finney, N.S.2    Jacobsen, E.N.3
  • 31
    • 0000303283 scopus 로고
    • Copolymerization
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 5328
    • Evans, D.A.1    Faul, M.M.2    Bilodeau, M.T.3    Anderson, B.A.4    Barnes, D.M.5
  • 32
    • 12044252836 scopus 로고
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 3641
    • Brookhart, M.1    Wagner, M.I.2    Balavoine, G.G.A.3    Haddau, H.A.4
  • 33
    • 33751133409 scopus 로고
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 2687
    • Rieck, H.1    Helmchen, G.2
  • 34
    • 0028209777 scopus 로고
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k)
    • (1994) Tetrahedron Asymm. , vol.5 , pp. 573
    • Von Matt, P.1    Loiseleur, O.2    Koch, G.3    Pfaltz, A.4    Lefeber, C.5    Feucht, T.6    Helmchen, G.7
  • 35
    • 33748496330 scopus 로고
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 462
    • Lloyd-Jones, G.C.1    Pfaltz, A.2
  • 36
    • 37049079396 scopus 로고
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1994) J. Chem. Soc., Perkin Trans. 1 , pp. 2065
    • Allen, J.V.1    Coote, S.J.2    Dawson, G.J.3    Frost, C.G.4    Martin, C.J.5    Williams, J.M.J.6
  • 37
    • 0028349296 scopus 로고
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 1523
    • Sprinz, J.1    Kiefer, M.2    Helmchen, G.3    Reggelin, M.4    Huttner, G.5    Walter, O.6    Zsolnai, L.7
  • 38
    • 33748227479 scopus 로고
    • Hydrosilylation
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1993) Angew. Chem., Int. Ed. Engl. , vol.32 , pp. 566
    • Von Matt, P.1    Pfaltz, A.2
  • 39
    • 0025883618 scopus 로고
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1991) Tetrahedron Asymm. , vol.2 , pp. 919
    • Brunner, H.1    Brandi, P.2
  • 40
    • 0002774258 scopus 로고
    • Transfer hydrogenation
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1990) J. Organomet. Chem. , vol.390
    • Brunner, H.1    Brandi, P.2
  • 41
    • 0029970526 scopus 로고    scopus 로고
    • Asymmetric Heck coupling
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 1381
    • Langer, T.1    Helmchen, G.2
  • 42
    • 33748617096 scopus 로고    scopus 로고
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1996) Angew. Chem., Int. Ed. Engl. , vol.35 , pp. 200
    • Loiseleur, O.1    Meier, P.2    Pfaltz, A.3
  • 43
    • 0029156882 scopus 로고
    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt, Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1995) J. Org. Chem. , vol.60 , pp. 4884
    • Denmark, S.E.1    Nakajima, N.2    Nicaise, O.J.-C.3    Faucher, A.-M.4    Edwards, J.P.5
  • 44
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    • For leading references on each class of reaction see: Allylic acetate displacement: (a) von Matt, P.; Lloyd-Jones, G. C.; Minidis, A. B. E.; Pfaltz, A.; Macko, L.; Neuburger, M.; Zehnder, M.; Rüegger, H.; Pregosin, P. S. Helv. Chim. Acta 1995, 78, 265. (b) Leutenegger, U.; Umbricht, G.; Fahrni, C.; von Matt, P.; Pfaltz, A. Tetrahedron 1992, 48, 2143. Allylic oxidation: (c) Gokhale, A. S.; Minidis, A. B. E.; Pfaltz, A. Tetrahedron Lett. 1995, 36, 1831. Hydrosilylation: (d) Nagashima, H.; Ueda, T.; Nishiyama, H.; Itoh, K. Chem. Lett. 1993, 347. (e) Nishiyama, H.; Yamaguchi, S.; Park, S.-B.; Itoh, K. Tetrahedron Asymm. 1993, 4, 143. (f) Nishiyama, H.; Yamaguchi, S.; Kondo, M.; Itoh, K. J. Org. Chem. 1992, 57, 4306. (g) Nishiyama, H.; Sakaguchi, H.; Nakamura, T.; Horihata, M.; Kondo, M.; Itoh, K. Organometallics 1989, 8, 846. Organometallic additions: (h) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C. J. Am. Chem. Soc. 1994, 116, 8797. Denmark, S. E.; Nicaise, O. J.-C. Chem. Commun. 1996, 999. [4 + 2] Cycloadditions: (j) Evans, D. A.; Murry, J. A.; von Matt, P.; Norcross, R. D.; Miller, S. J. Angew. Chem., Int. Ed. Engl. 1995, 34, 798. (k) Evans, D. A.; Miller, S. J.; Lectka, T. J. Am Chem. Soc. 1993, 115, 6460. Corey, E. J.; Wang, Z. Tetrahedron Lett. 1993, 34, 4001. Corey, E. J.; Ishihara, K. Tetrahedron Lett. 1992, 33, 6807. (n) Corey, E. J.; Imai, N.; Zhang, H.-Y. J. Am. Chem. Soc. 1991, 113, 728. Aziridination: (o) Hansen, K. B.; Finney, N. S.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1995, 34, 676. (p) Evans, D. A.; Faul, M. M.; Bilodeau, M. T.; Anderson, B. A.; Barnes, D. M. J. Am. Chem. Soc. 1993, 115, 5328. Copolymerization: (q) Brookhart, M.; Wagner, M. I.; Balavoine, G. G. A.; Haddau, H. A. J. Am. Chem. Soc. 1994, 116, 3641. In addition, aryl monooxazoline complexes have become popular ligands. For leading references see: Allylic acetate discplacements: (r) Rieck, H.; Helmchen, G. Angew. Chem., Int. Ed. Engl. 1995, 34, 2687. (s) von Matt, P.; Loiseleur, O.; Koch, G.; Pfaltz, A.; Lefeber, C.; Feucht, T.; Helmchen, G. Tetrahedron Asymm. 1994, 5, 573. (t) Lloyd-Jones, G. C.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1995, 34, 462. (u) Allen, J. V.; Coote, S. J.; Dawson, G. J.; Frost, C. G.; Martin, C. J. Williams, J. M. J. J. Chem. Soc., Perkin Trans. 1 1994, 2065. Sprinz, J.; Kiefer, M.; Helmchen, G.; Reggelin, M.; Huttner, G.; Walter, O.; Zsolnai, L. Tetrahedron Lett. 1994, 35, 1523. (w) von Matt, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1993, 32, 566. Hydrosilylation: Brunner, H.; Brandi, P. Tetrahedron Asymm. 1991, 2, 919. (y) Brunner, H.; Brandi, P. J. Organomet. Chem. 1990, 390, C81. Transfer hydrogenation: (z) Langer, T.; Helmchen, G. Tetrahedron Lett. 1996, 37, 1381. Asymmetric Heck coupling: (aa) Loiseleur, O.; Meier, P.; Pfaltz, A. Angew. Chem., Int. Ed. Engl. 1996, 35, 200. For a leading reference on the preparation of bis(oxazoline) ligands see: (bb) Denmark, S. E.; Nakajima, N.; Nicaise, O. J.-C.; Faucher, A.-M.; Edwards, J. P. J. Org. Chem. 1995, 60, 4884. For (phosphinoaryl)oxazolines see: (cc) Koch, G.; Lloyd-Jones, G. C.; Loiseleur, O.; Pfaltz, A.; Prétôt Schaffner, S.; Schnider, P.; von Matt, P. Recl. Trav. Chim. Pays-Bos 1995, 114, 206.
    • (1995) Recl. Trav. Chim. Pays-Bos , vol.114 , pp. 206
    • Koch, G.1    Lloyd-Jones, G.C.2    Loiseleur, O.3    Pfaltz, A.4    Prétôt Schaffner, S.5    Schnider, P.6    Von Matt, P.7
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    • For other studies showing the fluxional nature of bis(oxazoline) coordination see: (a) reference 13b. (b) Bolm, C.; Weickhardt, K.; Zehnder, M.; Ranff, T. Chem. Ber. 1991, 124, 1173.
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    • (a) Black, T. H. Aldrichim. Acta 1983, 16, 3. For details on the titration of diazomethane solutions see:
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    • (b) Arnedt, F. Organic Syntheses; Wiley: New York, 1943; Coll. Vol. II, 1943, p 165.
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    • (f) Ryabov, A. D. Inorg. Chem. 1987, 26, 1252. For reveiws see:
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    • Puddephatt, R. J., Ed.; Pergamon Press: New York
    • (k) Canty, A. J. Palladium-Carbon σ-Bonded Complexes. In Comprehensive Organometallic Chemistry II; Puddephatt, R. J., Ed.; Pergamon Press: New York, 1995; Vol. 9.
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    • Canty, A.J.1
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    • note
    • 2 requires C: 64.36; H: 4.87; Pd: 22.36. Found: C: 64.31; H: 4.83; Pd: 22.36. The use of this formula to calculate stoichiometry resulted in clean oxidative addition and recovery of dibenzylideneacetone.
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    • Reference 11a
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
  • 121
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    • Reference 13b.
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
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    • Pd
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
    • (1991) Helv. Chim. Acta , vol.74 , pp. 1
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  • 123
    • 0030600597 scopus 로고    scopus 로고
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
    • (1996) Organomet. Chem. , vol.507 , pp. 85
    • Nesper, R.1    Pregosin, P.2    Püntener, K.3    Wörle, M.4    Albinati, A.J.5
  • 124
    • 1542455688 scopus 로고    scopus 로고
    • Reference 3b
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
  • 125
    • 0000734193 scopus 로고
    • Zn
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
    • (1995) Acta. Crystallogr. , vol.C51 , pp. 1109
    • Zehnder, M.1    Neuburger, M.2    Von Matt, P.3    Pfaltz, A.4
  • 126
    • 1542455693 scopus 로고    scopus 로고
    • Reference 18c. Ni: W
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
  • 127
    • 21844513443 scopus 로고
    • Rh
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F.
    • (1995) Naturforsch. , vol.50 B , pp. 361
    • Lloyd-Jones, G.C.1    Pfaltz, A.Z.2
  • 128
    • 1542560187 scopus 로고    scopus 로고
    • Reference 2i Ru
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
  • 129
    • 37049077308 scopus 로고
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
    • (1995) J. Chem. Soc., Dalton Trans. , pp. 367
    • Bennett, S.1    Brown, S.M.2    Conole, G.3    Kessler, M.4    Rowling, S.5    Sinn, E.6    Woodward, S.7
  • 130
    • 0000499693 scopus 로고
    • Zr
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
    • (1995) Inorg. Chem. , vol.34 , pp. 4198
    • Szczepura, L.F.1    Maricich, S.M.2    See, R.F.3    Churchill, M.R.4    Takeuchi, K.J.5
  • 131
    • 33751156349 scopus 로고
    • Cu, Ni, Zn
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
    • (1995) Inorg. Chem. , vol.34 , pp. 2921
    • Cozzi, P.G.1    Floriam, C.2    Chiesi-Villa, A.3    Rizzoli, C.4
  • 132
    • 84949116784 scopus 로고
    • Pd
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
    • (1991) Helv. Chim. Acta , vol.74 , pp. 717
    • Bolm, C.1    Weickhardt, K.2    Zehnder, M.3    Glasmacher, D.4
  • 133
    • 1542560179 scopus 로고    scopus 로고
    • Reference 23b
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
  • 134
    • 1542560188 scopus 로고    scopus 로고
    • Reference 23e
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
  • 135
    • 1542455701 scopus 로고    scopus 로고
    • Reference 23f
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
  • 136
    • 1542560183 scopus 로고    scopus 로고
    • Reference 3r. Pt
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
  • 137
    • 0000207946 scopus 로고
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
    • (1991) Organometallics , vol.10 , pp. 1751
    • Michelin, R.A.1    Bertani, R.2    Mozzon, M.3    Bombieri, G.4    Benetollo, F.5    Angelici, R.J.6
  • 138
    • 37049089940 scopus 로고
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
    • (1993) J. Chem. Soc., Dalton Trans. , pp. 959
    • Michelen, R.A.1    Bertani, R.2    Mozzon, M.3    Bombieri, G.4    Benetollo, F.5    Angelici, R.J.6
  • 139
    • 0001351004 scopus 로고
    • Tc
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
    • (1994) Organometallics , vol.13 , pp. 1341
    • Michelen, R.A.1    Mozzon, M.2    Berin, P.3    Bertani, R.4    Benetollo, F.5    Bombieri, G.6    Aneglici, R.J.7
  • 140
    • 0000559290 scopus 로고
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
    • (1988) Inorg. Chem. , vol.27 , pp. 4208
    • Duatti, A.1    Marchi, A.2    Rossi, R.3    Magon, L.4    Deutsch, E.5    Bertolasi, V.6    Bellucci, F.7
  • 141
    • 0346316738 scopus 로고
    • Al, Ga, In
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
    • (1988) Inorg. Chim. Acta , vol.142 , pp. 55
    • Wilcox, B.E.1    Cooper, J.N.2    Elder, R.C.3    Deutsch, E.4
  • 142
    • 0001577833 scopus 로고
    • Ti, Zr, V: Ref 271. Re, Tc
    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
    • (1992) Inorg. Chem. , vol.31 , pp. 5408
    • Hoveyda, H.R.1    Karunaratne, V.2    Rettig, S.J.3    Orvig, C.4
  • 143
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    • For other crystal structures of bis(oxazoline)metal complexes see: Cu: (a) Reference 11a. (b) Reference 13b. (c) Hall, J.; Lehn, J.-M.; DeCian, A.; Fischer, J. Helv. Chim. Acta 1991, 74, 1. Pd: (d) Nesper, R.; Pregosin, P.; Püntener, K.; Wörle, M.; Albinati, A. J. Organomet. Chem. 1996, 507, 85. (e) Reference 3b. (f) Zehnder, M.; Neuburger, M.; von Matt, P.; Pfaltz, A. Acta. Crystallogr. 1995, C51, 1109. Zn: (g) Reference 18c. Ni: W: (h) Lloyd-Jones, G. C.; Pfaltz, A. Z. Naturforsch. 1995, 50b, 361. Rh: (i) Reference 2i Ru: (j) Bennett, S.; Brown, S. M.; Conole, G.; Kessler, M.; Rowling, S.; Sinn, E.; Woodward, S. J. Chem. Soc., Dalton Trans. 1995, 367. (k) Szczepura, L. F.; Maricich, S. M.; See, R. F.; Churchill, M. R.; Takeuchi K. J. Inorg. Chem. 1995, 34, 4198. Zr: (l) Cozzi, P. G.; Floriam C.; Chiesi-Villa A.; Rizzoli, C. Inorg. Chem. 1995, 34, 2921. For crystal structures of mono(oxazoline)metal complexes see: Cu, Ni, Zn: (m) Bolm, C.; Weickhardt, K.; Zehnder, M.; Glasmacher, D. Helv. Chim. Acta 1991, 74, 717. Pd: (n) Reference 23b. (o) Reference 23e. (p) Reference 23f. (q) Reference 3r. Pt: (r) Michelin, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. Organometallics 1991, 10, 1751. (s) Michelen, R. A.; Bertani, R.; Mozzon, M.; Bombieri, G.; Benetollo, F.; Angelici, R. J. J. Chem. Soc., Dalton Trans. 1993, 959. (t) Michelen, R. A.; Mozzon, M.; Berin, P.; Bertani, R.; Benetollo, F.; Bombieri, G.; Aneglici, R. J. Organometallics 1994, 13, 1341. Tc (u) Duatti, A.; Marchi, A.; Rossi, R.; Magon, L.; Deutsch, E.; Bertolasi, V.; Bellucci, F. Inorg. Chem. 1988, 27, 4208. (v) Wilcox B. E.; Cooper, J. N.; Elder, R. C.; Deutsch, E. Inorg. Chim. Acta 1988, 142, 55. Al, Ga, In: (w) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1992, 31, 5408. Ti, Zr, V: Ref 271. Re, Tc: Shuter, E.; Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J.; Orvig, C. Inorg. Chem. 1996, 35, 368.
    • (1996) Inorg. Chem. , vol.35 , pp. 368
    • Shuter, E.1    Hoveyda, H.R.2    Karunaratne, V.3    Rettig, S.J.4    Orvig, C.5
  • 147
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    • Nakamura, A.; Koyama, T.; Otsuka, S. Bull. Chem. Soc. Jpn. 1978, 51, 593. Additionally, these authors briefly mention attempting asymmetric cyclopropanation of styrene with ethyl diazoacetate and various palladium catalysts. No details are provided, though none of the catalysts provided enantiomerically enriched cyclopropanes.
    • (1978) Bull. Chem. Soc. Jpn. , vol.51 , pp. 593
    • Nakamura, A.1    Koyama, T.2    Otsuka, S.3
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    • and references therein. For reviews on metallocyclobutanes see
    • (b) Casey, C. P.; Shusterman, A. J. Organometallics 1985, 4, 736. and references therein. For reviews on metallocyclobutanes see:
    • (1985) Organometallics , vol.4 , pp. 736
    • Casey, C.P.1    Shusterman, A.J.2
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    • Reference 34d
    • (a) Reference 34d.
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    • note
    • (36) In a preliminary experiment, ethyl cinnamate, diazomethane (3.5 equiv), and 15b (25 mol %) were combined and after separation of the cyclopropane product, the catalyst could be recovered in two fractions: 42% mass recovery of pure (>90% by NMR) 15b and 29% mass recovery of impure 15b.


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