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Volumn 603, Issue 1, 2000, Pages 86-97

Direct ortho-palladation of 2-phenyl-2-oxazoline: Crystal structure of Cl2Pd(OCH2CH2N=C-Ph)2 and Cl(PPh3)Pd(OCH2CH2N=C-C6H 4)

Author keywords

2 phenyl 2 oxazoline; Cyclopalladated complexes; X ray study

Indexed keywords

STAPHYLOCOCCUS PHAGE 3A;

EID: 0002832351     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-328X(00)00133-9     Document Type: Article
Times cited : (44)

References (116)
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    • Representative examples of bisoxazoline use in catalysis: (a) H. Matsunaga, Y. Yamada, Ts. Ide, T. Ishizuka, T. Kunieda, Tetrahedron Asymm. 10 (1999) 3095. (b) D.A. Evans, E.J. Olhava, J.S. Johnson, J.M. Janey, Angew. Chem. Int. Ed. 37 (1998) 3372. (c) D.A. Evans, J.S. Johnson, J. Am. Chem. Soc. 120 (1998) 4895. (d) M.P. Sibi, J. Ji, J. Org. Chem. 62 (1997) 3800. (e) A. Chesney, M.R. Bryce, R.W.J. Chubb, A.S. Batsanov, J.A.K. Howard, Tetrahedron Asymm. 8 (1997) 2337. (f) Y. Uozumi, K. Kato, T. Hayashi. J. Am. Chem. Soc. 119 (1997) 5063. (g) A.K. Ghost, P. Mathivanan, J. Cappiello, Tetrahedron Lett. 37 (1996) 3815. (h) A.V. Bedekar, P.G. Andersson, Tetrahedron Lett. 37 (1996) 4073. (i) G. Desimoni, G. Faita, P.P. Righetti, N. Sardone, Tetrahedron 52 (1996) 12019. (j) P. von Matt, G.C. Lloyd-Jones, A.B.E. Minidis, A. Pfaltz, L. Macko, M. Neuburger, M. Zehnder, H. Ruegger, P.S. Pregosin, Helv. Chim. Acta 78 (1995) 265.
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    • Representative examples of bisoxazoline use in catalysis: (a) H. Matsunaga, Y. Yamada, Ts. Ide, T. Ishizuka, T. Kunieda, Tetrahedron Asymm. 10 (1999) 3095. (b) D.A. Evans, E.J. Olhava, J.S. Johnson, J.M. Janey, Angew. Chem. Int. Ed. 37 (1998) 3372. (c) D.A. Evans, J.S. Johnson, J. Am. Chem. Soc. 120 (1998) 4895. (d) M.P. Sibi, J. Ji, J. Org. Chem. 62 (1997) 3800. (e) A. Chesney, M.R. Bryce, R.W.J. Chubb, A.S. Batsanov, J.A.K. Howard, Tetrahedron Asymm. 8 (1997) 2337. (f) Y. Uozumi, K. Kato, T. Hayashi. J. Am. Chem. Soc. 119 (1997) 5063. (g) A.K. Ghost, P. Mathivanan, J. Cappiello, Tetrahedron Lett. 37 (1996) 3815. (h) A.V. Bedekar, P.G. Andersson, Tetrahedron Lett. 37 (1996) 4073. (i) G. Desimoni, G. Faita, P.P. Righetti, N. Sardone, Tetrahedron 52 (1996) 12019. (j) P. von Matt, G.C. Lloyd-Jones, A.B.E. Minidis, A. Pfaltz, L. Macko, M. Neuburger, M. Zehnder, H. Ruegger, P.S. Pregosin, Helv. Chim. Acta 78 (1995) 265.
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    • Representative examples of bisoxazoline use in catalysis: (a) H. Matsunaga, Y. Yamada, Ts. Ide, T. Ishizuka, T. Kunieda, Tetrahedron Asymm. 10 (1999) 3095. (b) D.A. Evans, E.J. Olhava, J.S. Johnson, J.M. Janey, Angew. Chem. Int. Ed. 37 (1998) 3372. (c) D.A. Evans, J.S. Johnson, J. Am. Chem. Soc. 120 (1998) 4895. (d) M.P. Sibi, J. Ji, J. Org. Chem. 62 (1997) 3800. (e) A. Chesney, M.R. Bryce, R.W.J. Chubb, A.S. Batsanov, J.A.K. Howard, Tetrahedron Asymm. 8 (1997) 2337. (f) Y. Uozumi, K. Kato, T. Hayashi. J. Am. Chem. Soc. 119 (1997) 5063. (g) A.K. Ghost, P. Mathivanan, J. Cappiello, Tetrahedron Lett. 37 (1996) 3815. (h) A.V. Bedekar, P.G. Andersson, Tetrahedron Lett. 37 (1996) 4073. (i) G. Desimoni, G. Faita, P.P. Righetti, N. Sardone, Tetrahedron 52 (1996) 12019. (j) P. von Matt, G.C. Lloyd-Jones, A.B.E. Minidis, A. Pfaltz, L. Macko, M. Neuburger, M. Zehnder, H. Ruegger, P.S. Pregosin, Helv. Chim. Acta 78 (1995) 265.
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  • 19
    • 0001478569 scopus 로고    scopus 로고
    • Some examples of phosphino-oxazoline use in catalysis: (a) X. Fang, M. Johannsen, S. Yao, N. Gathergood, R.G. Hazell, K.A. Jørgensen, J. Org. Chem. 64 (1999) 4844. (b) K. Selvakumar, M. Valentini, M. Worle, P.S. Pregosin, A. Albinati, Organometallics 18 (1999) 1207. (c) W. Zhang, Y.-I. Yoneda, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Asymm. 9 (1998) 3371. (d) Y. Nishibayashi, I. Takei, S. Uemura, M. Hidai, Organometallics 17 (1998) 3420. (e) B. Wiese, G. Helmchen, Tetrahedron Lett. 39 (1998) 5727. (f) R. Prétôt, A. Pfaltz, Angew. Chem. Int. Ed. 37 (1998) 323. (g) H.-J. Gais, H. Eichelmann, N. Spalthoff, F. Gerhards, M. Frank, G. Raabe, Tetrahedron Asymm. 8 (1998) 235. (h) A. Sudo, K. Saigo, J. Org. Chem. 62 (1997) 5508. (i) T. Sammakia, E.L. Stangeland, J. Org. Chem. 62 (1997) 6104. (j) K.H. Ahn, C.-W. Cho, J. Park, S. Lee, Tetrahedron Asymm. 8 (1997) 1179. (k) L. Ripa, A. Hallberg, J. Org. Chem. 62 (1997) 595. (l) Y. Nishibayashi, K. Segawa, H. Takada, K. Ohe, S. Uemura, Chem. Commun. (1996) 847. (m) W. Zhang, T. Hirao, I. Ikeda, Tetrahedron Lett. 37 (1996) 4545. (n) P.A. Evans, T.A. Brandt, Tetrahedron Lett. 37 (1996) 9143. (o) G.J. Dawson, J.M.J. Williams, Tetrahedron Lett. 36 (1995) 461. (p) I.C. Baldwin, J.M.J. Williams, R.P. Beskett, Tetrahedron Asymm. 6 (1995) 1515. (q) P. von Matt, O. Loiseleur, G. Koch, A. Pfaltz, C. Lefeber, T. Feucht, G. Helmchen, Tetrahedron Asymm. 5 (1994) 573. (r) P. von Matt, A. Pfaltz, Angew. Chem. Int. Ed. 32 (1993) 566.
    • (1999) Organometallics , vol.18 , pp. 1207
    • Selvakumar, K.1    Valentini, M.2    Worle, M.3    Pregosin, P.S.4    Albinati, A.5
  • 20
    • 0032476115 scopus 로고    scopus 로고
    • Some examples of phosphino-oxazoline use in catalysis: (a) X. Fang, M. Johannsen, S. Yao, N. Gathergood, R.G. Hazell, K.A. Jørgensen, J. Org. Chem. 64 (1999) 4844. (b) K. Selvakumar, M. Valentini, M. Worle, P.S. Pregosin, A. Albinati, Organometallics 18 (1999) 1207. (c) W. Zhang, Y.-I. Yoneda, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Asymm. 9 (1998) 3371. (d) Y. Nishibayashi, I. Takei, S. Uemura, M. Hidai, Organometallics 17 (1998) 3420. (e) B. Wiese, G. Helmchen, Tetrahedron Lett. 39 (1998) 5727. (f) R. Prétôt, A. Pfaltz, Angew. Chem. Int. Ed. 37 (1998) 323. (g) H.-J. Gais, H. Eichelmann, N. Spalthoff, F. Gerhards, M. Frank, G. Raabe, Tetrahedron Asymm. 8 (1998) 235. (h) A. Sudo, K. Saigo, J. Org. Chem. 62 (1997) 5508. (i) T. Sammakia, E.L. Stangeland, J. Org. Chem. 62 (1997) 6104. (j) K.H. Ahn, C.-W. Cho, J. Park, S. Lee, Tetrahedron Asymm. 8 (1997) 1179. (k) L. Ripa, A. Hallberg, J. Org. Chem. 62 (1997) 595. (l) Y. Nishibayashi, K. Segawa, H. Takada, K. Ohe, S. Uemura, Chem. Commun. (1996) 847. (m) W. Zhang, T. Hirao, I. Ikeda, Tetrahedron Lett. 37 (1996) 4545. (n) P.A. Evans, T.A. Brandt, Tetrahedron Lett. 37 (1996) 9143. (o) G.J. Dawson, J.M.J. Williams, Tetrahedron Lett. 36 (1995) 461. (p) I.C. Baldwin, J.M.J. Williams, R.P. Beskett, Tetrahedron Asymm. 6 (1995) 1515. (q) P. von Matt, O. Loiseleur, G. Koch, A. Pfaltz, C. Lefeber, T. Feucht, G. Helmchen, Tetrahedron Asymm. 5 (1994) 573. (r) P. von Matt, A. Pfaltz, Angew. Chem. Int. Ed. 32 (1993) 566.
    • (1998) Tetrahedron Asymm. , vol.9 , pp. 3371
    • Zhang, W.1    Yoneda, Y.-I.2    Kida, T.3    Nakatsuji, Y.4    Ikeda, I.5
  • 21
    • 0001343261 scopus 로고    scopus 로고
    • Some examples of phosphino-oxazoline use in catalysis: (a) X. Fang, M. Johannsen, S. Yao, N. Gathergood, R.G. Hazell, K.A. Jørgensen, J. Org. Chem. 64 (1999) 4844. (b) K. Selvakumar, M. Valentini, M. Worle, P.S. Pregosin, A. Albinati, Organometallics 18 (1999) 1207. (c) W. Zhang, Y.-I. Yoneda, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Asymm. 9 (1998) 3371. (d) Y. Nishibayashi, I. Takei, S. Uemura, M. Hidai, Organometallics 17 (1998) 3420. (e) B. Wiese, G. Helmchen, Tetrahedron Lett. 39 (1998) 5727. (f) R. Prétôt, A. Pfaltz, Angew. Chem. Int. Ed. 37 (1998) 323. (g) H.-J. Gais, H. Eichelmann, N. Spalthoff, F. Gerhards, M. Frank, G. Raabe, Tetrahedron Asymm. 8 (1998) 235. (h) A. Sudo, K. Saigo, J. Org. Chem. 62 (1997) 5508. (i) T. Sammakia, E.L. Stangeland, J. Org. Chem. 62 (1997) 6104. (j) K.H. Ahn, C.-W. Cho, J. Park, S. Lee, Tetrahedron Asymm. 8 (1997) 1179. (k) L. Ripa, A. Hallberg, J. Org. Chem. 62 (1997) 595. (l) Y. Nishibayashi, K. Segawa, H. Takada, K. Ohe, S. Uemura, Chem. Commun. (1996) 847. (m) W. Zhang, T. Hirao, I. Ikeda, Tetrahedron Lett. 37 (1996) 4545. (n) P.A. Evans, T.A. Brandt, Tetrahedron Lett. 37 (1996) 9143. (o) G.J. Dawson, J.M.J. Williams, Tetrahedron Lett. 36 (1995) 461. (p) I.C. Baldwin, J.M.J. Williams, R.P. Beskett, Tetrahedron Asymm. 6 (1995) 1515. (q) P. von Matt, O. Loiseleur, G. Koch, A. Pfaltz, C. Lefeber, T. Feucht, G. Helmchen, Tetrahedron Asymm. 5 (1994) 573. (r) P. von Matt, A. Pfaltz, Angew. Chem. Int. Ed. 32 (1993) 566.
    • (1998) Organometallics , vol.17 , pp. 3420
    • Nishibayashi, Y.1    Takei, I.2    Uemura, S.3    Hidai, M.4
  • 22
    • 0032490952 scopus 로고    scopus 로고
    • Some examples of phosphino-oxazoline use in catalysis: (a) X. Fang, M. Johannsen, S. Yao, N. Gathergood, R.G. Hazell, K.A. Jørgensen, J. Org. Chem. 64 (1999) 4844. (b) K. Selvakumar, M. Valentini, M. Worle, P.S. Pregosin, A. Albinati, Organometallics 18 (1999) 1207. (c) W. Zhang, Y.-I. Yoneda, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Asymm. 9 (1998) 3371. (d) Y. Nishibayashi, I. Takei, S. Uemura, M. Hidai, Organometallics 17 (1998) 3420. (e) B. Wiese, G. Helmchen, Tetrahedron Lett. 39 (1998) 5727. (f) R. Prétôt, A. Pfaltz, Angew. Chem. Int. Ed. 37 (1998) 323. (g) H.-J. Gais, H. Eichelmann, N. Spalthoff, F. Gerhards, M. Frank, G. Raabe, Tetrahedron Asymm. 8 (1998) 235. (h) A. Sudo, K. Saigo, J. Org. Chem. 62 (1997) 5508. (i) T. Sammakia, E.L. Stangeland, J. Org. Chem. 62 (1997) 6104. (j) K.H. Ahn, C.-W. Cho, J. Park, S. Lee, Tetrahedron Asymm. 8 (1997) 1179. (k) L. Ripa, A. Hallberg, J. Org. Chem. 62 (1997) 595. (l) Y. Nishibayashi, K. Segawa, H. Takada, K. Ohe, S. Uemura, Chem. Commun. (1996) 847. (m) W. Zhang, T. Hirao, I. Ikeda, Tetrahedron Lett. 37 (1996) 4545. (n) P.A. Evans, T.A. Brandt, Tetrahedron Lett. 37 (1996) 9143. (o) G.J. Dawson, J.M.J. Williams, Tetrahedron Lett. 36 (1995) 461. (p) I.C. Baldwin, J.M.J. Williams, R.P. Beskett, Tetrahedron Asymm. 6 (1995) 1515. (q) P. von Matt, O. Loiseleur, G. Koch, A. Pfaltz, C. Lefeber, T. Feucht, G. Helmchen, Tetrahedron Asymm. 5 (1994) 573. (r) P. von Matt, A. Pfaltz, Angew. Chem. Int. Ed. 32 (1993) 566.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 5727
    • Wiese, B.1    Helmchen, G.2
  • 23
    • 0032536559 scopus 로고    scopus 로고
    • Some examples of phosphino-oxazoline use in catalysis: (a) X. Fang, M. Johannsen, S. Yao, N. Gathergood, R.G. Hazell, K.A. Jørgensen, J. Org. Chem. 64 (1999) 4844. (b) K. Selvakumar, M. Valentini, M. Worle, P.S. Pregosin, A. Albinati, Organometallics 18 (1999) 1207. (c) W. Zhang, Y.-I. Yoneda, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Asymm. 9 (1998) 3371. (d) Y. Nishibayashi, I. Takei, S. Uemura, M. Hidai, Organometallics 17 (1998) 3420. (e) B. Wiese, G. Helmchen, Tetrahedron Lett. 39 (1998) 5727. (f) R. Prétôt, A. Pfaltz, Angew. Chem. Int. Ed. 37 (1998) 323. (g) H.-J. Gais, H. Eichelmann, N. Spalthoff, F. Gerhards, M. Frank, G. Raabe, Tetrahedron Asymm. 8 (1998) 235. (h) A. Sudo, K. Saigo, J. Org. Chem. 62 (1997) 5508. (i) T. Sammakia, E.L. Stangeland, J. Org. Chem. 62 (1997) 6104. (j) K.H. Ahn, C.-W. Cho, J. Park, S. Lee, Tetrahedron Asymm. 8 (1997) 1179. (k) L. Ripa, A. Hallberg, J. Org. Chem. 62 (1997) 595. (l) Y. Nishibayashi, K. Segawa, H. Takada, K. Ohe, S. Uemura, Chem. Commun. (1996) 847. (m) W. Zhang, T. Hirao, I. Ikeda, Tetrahedron Lett. 37 (1996) 4545. (n) P.A. Evans, T.A. Brandt, Tetrahedron Lett. 37 (1996) 9143. (o) G.J. Dawson, J.M.J. Williams, Tetrahedron Lett. 36 (1995) 461. (p) I.C. Baldwin, J.M.J. Williams, R.P. Beskett, Tetrahedron Asymm. 6 (1995) 1515. (q) P. von Matt, O. Loiseleur, G. Koch, A. Pfaltz, C. Lefeber, T. Feucht, G. Helmchen, Tetrahedron Asymm. 5 (1994) 573. (r) P. von Matt, A. Pfaltz, Angew. Chem. Int. Ed. 32 (1993) 566.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 323
    • Prétôt, R.1    Pfaltz, A.2
  • 24
    • 0032579177 scopus 로고    scopus 로고
    • Some examples of phosphino-oxazoline use in catalysis: (a) X. Fang, M. Johannsen, S. Yao, N. Gathergood, R.G. Hazell, K.A. Jørgensen, J. Org. Chem. 64 (1999) 4844. (b) K. Selvakumar, M. Valentini, M. Worle, P.S. Pregosin, A. Albinati, Organometallics 18 (1999) 1207. (c) W. Zhang, Y.-I. Yoneda, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Asymm. 9 (1998) 3371. (d) Y. Nishibayashi, I. Takei, S. Uemura, M. Hidai, Organometallics 17 (1998) 3420. (e) B. Wiese, G. Helmchen, Tetrahedron Lett. 39 (1998) 5727. (f) R. Prétôt, A. Pfaltz, Angew. Chem. Int. Ed. 37 (1998) 323. (g) H.-J. Gais, H. Eichelmann, N. Spalthoff, F. Gerhards, M. Frank, G. Raabe, Tetrahedron Asymm. 8 (1998) 235. (h) A. Sudo, K. Saigo, J. Org. Chem. 62 (1997) 5508. (i) T. Sammakia, E.L. Stangeland, J. Org. Chem. 62 (1997) 6104. (j) K.H. Ahn, C.-W. Cho, J. Park, S. Lee, Tetrahedron Asymm. 8 (1997) 1179. (k) L. Ripa, A. Hallberg, J. Org. Chem. 62 (1997) 595. (l) Y. Nishibayashi, K. Segawa, H. Takada, K. Ohe, S. Uemura, Chem. Commun. (1996) 847. (m) W. Zhang, T. Hirao, I. Ikeda, Tetrahedron Lett. 37 (1996) 4545. (n) P.A. Evans, T.A. Brandt, Tetrahedron Lett. 37 (1996) 9143. (o) G.J. Dawson, J.M.J. Williams, Tetrahedron Lett. 36 (1995) 461. (p) I.C. Baldwin, J.M.J. Williams, R.P. Beskett, Tetrahedron Asymm. 6 (1995) 1515. (q) P. von Matt, O. Loiseleur, G. Koch, A. Pfaltz, C. Lefeber, T. Feucht, G. Helmchen, Tetrahedron Asymm. 5 (1994) 573. (r) P. von Matt, A. Pfaltz, Angew. Chem. Int. Ed. 32 (1993) 566.
    • (1998) Tetrahedron Asymm. , vol.8 , pp. 235
    • Gais, H.-J.1    Eichelmann, H.2    Spalthoff, N.3    Gerhards, F.4    Frank, M.5    Raabe, G.6
  • 25
    • 0000187354 scopus 로고    scopus 로고
    • Some examples of phosphino-oxazoline use in catalysis: (a) X. Fang, M. Johannsen, S. Yao, N. Gathergood, R.G. Hazell, K.A. Jørgensen, J. Org. Chem. 64 (1999) 4844. (b) K. Selvakumar, M. Valentini, M. Worle, P.S. Pregosin, A. Albinati, Organometallics 18 (1999) 1207. (c) W. Zhang, Y.-I. Yoneda, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Asymm. 9 (1998) 3371. (d) Y. Nishibayashi, I. Takei, S. Uemura, M. Hidai, Organometallics 17 (1998) 3420. (e) B. Wiese, G. Helmchen, Tetrahedron Lett. 39 (1998) 5727. (f) R. Prétôt, A. Pfaltz, Angew. Chem. Int. Ed. 37 (1998) 323. (g) H.-J. Gais, H. Eichelmann, N. Spalthoff, F. Gerhards, M. Frank, G. Raabe, Tetrahedron Asymm. 8 (1998) 235. (h) A. Sudo, K. Saigo, J. Org. Chem. 62 (1997) 5508. (i) T. Sammakia, E.L. Stangeland, J. Org. Chem. 62 (1997) 6104. (j) K.H. Ahn, C.-W. Cho, J. Park, S. Lee, Tetrahedron Asymm. 8 (1997) 1179. (k) L. Ripa, A. Hallberg, J. Org. Chem. 62 (1997) 595. (l) Y. Nishibayashi, K. Segawa, H. Takada, K. Ohe, S. Uemura, Chem. Commun. (1996) 847. (m) W. Zhang, T. Hirao, I. Ikeda, Tetrahedron Lett. 37 (1996) 4545. (n) P.A. Evans, T.A. Brandt, Tetrahedron Lett. 37 (1996) 9143. (o) G.J. Dawson, J.M.J. Williams, Tetrahedron Lett. 36 (1995) 461. (p) I.C. Baldwin, J.M.J. Williams, R.P. Beskett, Tetrahedron Asymm. 6 (1995) 1515. (q) P. von Matt, O. Loiseleur, G. Koch, A. Pfaltz, C. Lefeber, T. Feucht, G. Helmchen, Tetrahedron Asymm. 5 (1994) 573. (r) P. von Matt, A. Pfaltz, Angew. Chem. Int. Ed. 32 (1993) 566.
    • (1997) J. Org. Chem. , vol.62 , pp. 5508
    • Sudo, A.1    Saigo, K.2
  • 26
    • 0001586112 scopus 로고    scopus 로고
    • Some examples of phosphino-oxazoline use in catalysis: (a) X. Fang, M. Johannsen, S. Yao, N. Gathergood, R.G. Hazell, K.A. Jørgensen, J. Org. Chem. 64 (1999) 4844. (b) K. Selvakumar, M. Valentini, M. Worle, P.S. Pregosin, A. Albinati, Organometallics 18 (1999) 1207. (c) W. Zhang, Y.-I. Yoneda, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Asymm. 9 (1998) 3371. (d) Y. Nishibayashi, I. Takei, S. Uemura, M. Hidai, Organometallics 17 (1998) 3420. (e) B. Wiese, G. Helmchen, Tetrahedron Lett. 39 (1998) 5727. (f) R. Prétôt, A. Pfaltz, Angew. Chem. Int. Ed. 37 (1998) 323. (g) H.-J. Gais, H. Eichelmann, N. Spalthoff, F. Gerhards, M. Frank, G. Raabe, Tetrahedron Asymm. 8 (1998) 235. (h) A. Sudo, K. Saigo, J. Org. Chem. 62 (1997) 5508. (i) T. Sammakia, E.L. Stangeland, J. Org. Chem. 62 (1997) 6104. (j) K.H. Ahn, C.-W. Cho, J. Park, S. Lee, Tetrahedron Asymm. 8 (1997) 1179. (k) L. Ripa, A. Hallberg, J. Org. Chem. 62 (1997) 595. (l) Y. Nishibayashi, K. Segawa, H. Takada, K. Ohe, S. Uemura, Chem. Commun. (1996) 847. (m) W. Zhang, T. Hirao, I. Ikeda, Tetrahedron Lett. 37 (1996) 4545. (n) P.A. Evans, T.A. Brandt, Tetrahedron Lett. 37 (1996) 9143. (o) G.J. Dawson, J.M.J. Williams, Tetrahedron Lett. 36 (1995) 461. (p) I.C. Baldwin, J.M.J. Williams, R.P. Beskett, Tetrahedron Asymm. 6 (1995) 1515. (q) P. von Matt, O. Loiseleur, G. Koch, A. Pfaltz, C. Lefeber, T. Feucht, G. Helmchen, Tetrahedron Asymm. 5 (1994) 573. (r) P. von Matt, A. Pfaltz, Angew. Chem. Int. Ed. 32 (1993) 566.
    • (1997) J. Org. Chem. , vol.62 , pp. 6104
    • Sammakia, T.1    Stangeland, E.L.2
  • 27
    • 0030894667 scopus 로고    scopus 로고
    • Some examples of phosphino-oxazoline use in catalysis: (a) X. Fang, M. Johannsen, S. Yao, N. Gathergood, R.G. Hazell, K.A. Jørgensen, J. Org. Chem. 64 (1999) 4844. (b) K. Selvakumar, M. Valentini, M. Worle, P.S. Pregosin, A. Albinati, Organometallics 18 (1999) 1207. (c) W. Zhang, Y.-I. Yoneda, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Asymm. 9 (1998) 3371. (d) Y. Nishibayashi, I. Takei, S. Uemura, M. Hidai, Organometallics 17 (1998) 3420. (e) B. Wiese, G. Helmchen, Tetrahedron Lett. 39 (1998) 5727. (f) R. Prétôt, A. Pfaltz, Angew. Chem. Int. Ed. 37 (1998) 323. (g) H.-J. Gais, H. Eichelmann, N. Spalthoff, F. Gerhards, M. Frank, G. Raabe, Tetrahedron Asymm. 8 (1998) 235. (h) A. Sudo, K. Saigo, J. Org. Chem. 62 (1997) 5508. (i) T. Sammakia, E.L. Stangeland, J. Org. Chem. 62 (1997) 6104. (j) K.H. Ahn, C.-W. Cho, J. Park, S. Lee, Tetrahedron Asymm. 8 (1997) 1179. (k) L. Ripa, A. Hallberg, J. Org. Chem. 62 (1997) 595. (l) Y. Nishibayashi, K. Segawa, H. Takada, K. Ohe, S. Uemura, Chem. Commun. (1996) 847. (m) W. Zhang, T. Hirao, I. Ikeda, Tetrahedron Lett. 37 (1996) 4545. (n) P.A. Evans, T.A. Brandt, Tetrahedron Lett. 37 (1996) 9143. (o) G.J. Dawson, J.M.J. Williams, Tetrahedron Lett. 36 (1995) 461. (p) I.C. Baldwin, J.M.J. Williams, R.P. Beskett, Tetrahedron Asymm. 6 (1995) 1515. (q) P. von Matt, O. Loiseleur, G. Koch, A. Pfaltz, C. Lefeber, T. Feucht, G. Helmchen, Tetrahedron Asymm. 5 (1994) 573. (r) P. von Matt, A. Pfaltz, Angew. Chem. Int. Ed. 32 (1993) 566.
    • (1997) Tetrahedron Asymm. , vol.8 , pp. 1179
    • Ahn, K.H.1    Cho, C.-W.2    Park, J.3    Lee, S.4
  • 28
    • 0001387445 scopus 로고    scopus 로고
    • Some examples of phosphino-oxazoline use in catalysis: (a) X. Fang, M. Johannsen, S. Yao, N. Gathergood, R.G. Hazell, K.A. Jørgensen, J. Org. Chem. 64 (1999) 4844. (b) K. Selvakumar, M. Valentini, M. Worle, P.S. Pregosin, A. Albinati, Organometallics 18 (1999) 1207. (c) W. Zhang, Y.-I. Yoneda, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Asymm. 9 (1998) 3371. (d) Y. Nishibayashi, I. Takei, S. Uemura, M. Hidai, Organometallics 17 (1998) 3420. (e) B. Wiese, G. Helmchen, Tetrahedron Lett. 39 (1998) 5727. (f) R. Prétôt, A. Pfaltz, Angew. Chem. Int. Ed. 37 (1998) 323. (g) H.-J. Gais, H. Eichelmann, N. Spalthoff, F. Gerhards, M. Frank, G. Raabe, Tetrahedron Asymm. 8 (1998) 235. (h) A. Sudo, K. Saigo, J. Org. Chem. 62 (1997) 5508. (i) T. Sammakia, E.L. Stangeland, J. Org. Chem. 62 (1997) 6104. (j) K.H. Ahn, C.-W. Cho, J. Park, S. Lee, Tetrahedron Asymm. 8 (1997) 1179. (k) L. Ripa, A. Hallberg, J. Org. Chem. 62 (1997) 595. (l) Y. Nishibayashi, K. Segawa, H. Takada, K. Ohe, S. Uemura, Chem. Commun. (1996) 847. (m) W. Zhang, T. Hirao, I. Ikeda, Tetrahedron Lett. 37 (1996) 4545. (n) P.A. Evans, T.A. Brandt, Tetrahedron Lett. 37 (1996) 9143. (o) G.J. Dawson, J.M.J. Williams, Tetrahedron Lett. 36 (1995) 461. (p) I.C. Baldwin, J.M.J. Williams, R.P. Beskett, Tetrahedron Asymm. 6 (1995) 1515. (q) P. von Matt, O. Loiseleur, G. Koch, A. Pfaltz, C. Lefeber, T. Feucht, G. Helmchen, Tetrahedron Asymm. 5 (1994) 573. (r) P. von Matt, A. Pfaltz, Angew. Chem. Int. Ed. 32 (1993) 566.
    • (1997) J. Org. Chem. , vol.62 , pp. 595
    • Ripa, L.1    Hallberg, A.2
  • 29
    • 0000398912 scopus 로고    scopus 로고
    • Some examples of phosphino-oxazoline use in catalysis: (a) X. Fang, M. Johannsen, S. Yao, N. Gathergood, R.G. Hazell, K.A. Jørgensen, J. Org. Chem. 64 (1999) 4844. (b) K. Selvakumar, M. Valentini, M. Worle, P.S. Pregosin, A. Albinati, Organometallics 18 (1999) 1207. (c) W. Zhang, Y.-I. Yoneda, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Asymm. 9 (1998) 3371. (d) Y. Nishibayashi, I. Takei, S. Uemura, M. Hidai, Organometallics 17 (1998) 3420. (e) B. Wiese, G. Helmchen, Tetrahedron Lett. 39 (1998) 5727. (f) R. Prétôt, A. Pfaltz, Angew. Chem. Int. Ed. 37 (1998) 323. (g) H.-J. Gais, H. Eichelmann, N. Spalthoff, F. Gerhards, M. Frank, G. Raabe, Tetrahedron Asymm. 8 (1998) 235. (h) A. Sudo, K. Saigo, J. Org. Chem. 62 (1997) 5508. (i) T. Sammakia, E.L. Stangeland, J. Org. Chem. 62 (1997) 6104. (j) K.H. Ahn, C.-W. Cho, J. Park, S. Lee, Tetrahedron Asymm. 8 (1997) 1179. (k) L. Ripa, A. Hallberg, J. Org. Chem. 62 (1997) 595. (l) Y. Nishibayashi, K. Segawa, H. Takada, K. Ohe, S. Uemura, Chem. Commun. (1996) 847. (m) W. Zhang, T. Hirao, I. Ikeda, Tetrahedron Lett. 37 (1996) 4545. (n) P.A. Evans, T.A. Brandt, Tetrahedron Lett. 37 (1996) 9143. (o) G.J. Dawson, J.M.J. Williams, Tetrahedron Lett. 36 (1995) 461. (p) I.C. Baldwin, J.M.J. Williams, R.P. Beskett, Tetrahedron Asymm. 6 (1995) 1515. (q) P. von Matt, O. Loiseleur, G. Koch, A. Pfaltz, C. Lefeber, T. Feucht, G. Helmchen, Tetrahedron Asymm. 5 (1994) 573. (r) P. von Matt, A. Pfaltz, Angew. Chem. Int. Ed. 32 (1993) 566.
    • (1996) Chem. Commun. , pp. 847
    • Nishibayashi, Y.1    Segawa, K.2    Takada, H.3    Ohe, K.4    Uemura, S.5
  • 30
    • 0030600179 scopus 로고    scopus 로고
    • Some examples of phosphino-oxazoline use in catalysis: (a) X. Fang, M. Johannsen, S. Yao, N. Gathergood, R.G. Hazell, K.A. Jørgensen, J. Org. Chem. 64 (1999) 4844. (b) K. Selvakumar, M. Valentini, M. Worle, P.S. Pregosin, A. Albinati, Organometallics 18 (1999) 1207. (c) W. Zhang, Y.-I. Yoneda, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Asymm. 9 (1998) 3371. (d) Y. Nishibayashi, I. Takei, S. Uemura, M. Hidai, Organometallics 17 (1998) 3420. (e) B. Wiese, G. Helmchen, Tetrahedron Lett. 39 (1998) 5727. (f) R. Prétôt, A. Pfaltz, Angew. Chem. Int. Ed. 37 (1998) 323. (g) H.-J. Gais, H. Eichelmann, N. Spalthoff, F. Gerhards, M. Frank, G. Raabe, Tetrahedron Asymm. 8 (1998) 235. (h) A. Sudo, K. Saigo, J. Org. Chem. 62 (1997) 5508. (i) T. Sammakia, E.L. Stangeland, J. Org. Chem. 62 (1997) 6104. (j) K.H. Ahn, C.-W. Cho, J. Park, S. Lee, Tetrahedron Asymm. 8 (1997) 1179. (k) L. Ripa, A. Hallberg, J. Org. Chem. 62 (1997) 595. (l) Y. Nishibayashi, K. Segawa, H. Takada, K. Ohe, S. Uemura, Chem. Commun. (1996) 847. (m) W. Zhang, T. Hirao, I. Ikeda, Tetrahedron Lett. 37 (1996) 4545. (n) P.A. Evans, T.A. Brandt, Tetrahedron Lett. 37 (1996) 9143. (o) G.J. Dawson, J.M.J. Williams, Tetrahedron Lett. 36 (1995) 461. (p) I.C. Baldwin, J.M.J. Williams, R.P. Beskett, Tetrahedron Asymm. 6 (1995) 1515. (q) P. von Matt, O. Loiseleur, G. Koch, A. Pfaltz, C. Lefeber, T. Feucht, G. Helmchen, Tetrahedron Asymm. 5 (1994) 573. (r) P. von Matt, A. Pfaltz, Angew. Chem. Int. Ed. 32 (1993) 566.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 4545
    • Zhang, W.1    Hirao, T.2    Ikeda, I.3
  • 31
    • 0030590966 scopus 로고    scopus 로고
    • Some examples of phosphino-oxazoline use in catalysis: (a) X. Fang, M. Johannsen, S. Yao, N. Gathergood, R.G. Hazell, K.A. Jørgensen, J. Org. Chem. 64 (1999) 4844. (b) K. Selvakumar, M. Valentini, M. Worle, P.S. Pregosin, A. Albinati, Organometallics 18 (1999) 1207. (c) W. Zhang, Y.-I. Yoneda, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Asymm. 9 (1998) 3371. (d) Y. Nishibayashi, I. Takei, S. Uemura, M. Hidai, Organometallics 17 (1998) 3420. (e) B. Wiese, G. Helmchen, Tetrahedron Lett. 39 (1998) 5727. (f) R. Prétôt, A. Pfaltz, Angew. Chem. Int. Ed. 37 (1998) 323. (g) H.-J. Gais, H. Eichelmann, N. Spalthoff, F. Gerhards, M. Frank, G. Raabe, Tetrahedron Asymm. 8 (1998) 235. (h) A. Sudo, K. Saigo, J. Org. Chem. 62 (1997) 5508. (i) T. Sammakia, E.L. Stangeland, J. Org. Chem. 62 (1997) 6104. (j) K.H. Ahn, C.-W. Cho, J. Park, S. Lee, Tetrahedron Asymm. 8 (1997) 1179. (k) L. Ripa, A. Hallberg, J. Org. Chem. 62 (1997) 595. (l) Y. Nishibayashi, K. Segawa, H. Takada, K. Ohe, S. Uemura, Chem. Commun. (1996) 847. (m) W. Zhang, T. Hirao, I. Ikeda, Tetrahedron Lett. 37 (1996) 4545. (n) P.A. Evans, T.A. Brandt, Tetrahedron Lett. 37 (1996) 9143. (o) G.J. Dawson, J.M.J. Williams, Tetrahedron Lett. 36 (1995) 461. (p) I.C. Baldwin, J.M.J. Williams, R.P. Beskett, Tetrahedron Asymm. 6 (1995) 1515. (q) P. von Matt, O. Loiseleur, G. Koch, A. Pfaltz, C. Lefeber, T. Feucht, G. Helmchen, Tetrahedron Asymm. 5 (1994) 573. (r) P. von Matt, A. Pfaltz, Angew. Chem. Int. Ed. 32 (1993) 566.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 9143
    • Evans, P.A.1    Brandt, T.A.2
  • 32
    • 0028816229 scopus 로고
    • Some examples of phosphino-oxazoline use in catalysis: (a) X. Fang, M. Johannsen, S. Yao, N. Gathergood, R.G. Hazell, K.A. Jørgensen, J. Org. Chem. 64 (1999) 4844. (b) K. Selvakumar, M. Valentini, M. Worle, P.S. Pregosin, A. Albinati, Organometallics 18 (1999) 1207. (c) W. Zhang, Y.-I. Yoneda, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Asymm. 9 (1998) 3371. (d) Y. Nishibayashi, I. Takei, S. Uemura, M. Hidai, Organometallics 17 (1998) 3420. (e) B. Wiese, G. Helmchen, Tetrahedron Lett. 39 (1998) 5727. (f) R. Prétôt, A. Pfaltz, Angew. Chem. Int. Ed. 37 (1998) 323. (g) H.-J. Gais, H. Eichelmann, N. Spalthoff, F. Gerhards, M. Frank, G. Raabe, Tetrahedron Asymm. 8 (1998) 235. (h) A. Sudo, K. Saigo, J. Org. Chem. 62 (1997) 5508. (i) T. Sammakia, E.L. Stangeland, J. Org. Chem. 62 (1997) 6104. (j) K.H. Ahn, C.-W. Cho, J. Park, S. Lee, Tetrahedron Asymm. 8 (1997) 1179. (k) L. Ripa, A. Hallberg, J. Org. Chem. 62 (1997) 595. (l) Y. Nishibayashi, K. Segawa, H. Takada, K. Ohe, S. Uemura, Chem. Commun. (1996) 847. (m) W. Zhang, T. Hirao, I. Ikeda, Tetrahedron Lett. 37 (1996) 4545. (n) P.A. Evans, T.A. Brandt, Tetrahedron Lett. 37 (1996) 9143. (o) G.J. Dawson, J.M.J. Williams, Tetrahedron Lett. 36 (1995) 461. (p) I.C. Baldwin, J.M.J. Williams, R.P. Beskett, Tetrahedron Asymm. 6 (1995) 1515. (q) P. von Matt, O. Loiseleur, G. Koch, A. Pfaltz, C. Lefeber, T. Feucht, G. Helmchen, Tetrahedron Asymm. 5 (1994) 573. (r) P. von Matt, A. Pfaltz, Angew. Chem. Int. Ed. 32 (1993) 566.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 461
    • Dawson, G.J.1    Williams, J.M.J.2
  • 33
    • 0029096513 scopus 로고
    • Some examples of phosphino-oxazoline use in catalysis: (a) X. Fang, M. Johannsen, S. Yao, N. Gathergood, R.G. Hazell, K.A. Jørgensen, J. Org. Chem. 64 (1999) 4844. (b) K. Selvakumar, M. Valentini, M. Worle, P.S. Pregosin, A. Albinati, Organometallics 18 (1999) 1207. (c) W. Zhang, Y.-I. Yoneda, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Asymm. 9 (1998) 3371. (d) Y. Nishibayashi, I. Takei, S. Uemura, M. Hidai, Organometallics 17 (1998) 3420. (e) B. Wiese, G. Helmchen, Tetrahedron Lett. 39 (1998) 5727. (f) R. Prétôt, A. Pfaltz, Angew. Chem. Int. Ed. 37 (1998) 323. (g) H.-J. Gais, H. Eichelmann, N. Spalthoff, F. Gerhards, M. Frank, G. Raabe, Tetrahedron Asymm. 8 (1998) 235. (h) A. Sudo, K. Saigo, J. Org. Chem. 62 (1997) 5508. (i) T. Sammakia, E.L. Stangeland, J. Org. Chem. 62 (1997) 6104. (j) K.H. Ahn, C.-W. Cho, J. Park, S. Lee, Tetrahedron Asymm. 8 (1997) 1179. (k) L. Ripa, A. Hallberg, J. Org. Chem. 62 (19(l) Y. Nishibayashi, K. Segawa, H. Takada, K. Ohe, S. Uemura, Chem. Commun. (1996) 847. (m) W. Zhang, T. Hirao, I. Ikeda, Tetrahedron Lett. 37 (1996) 4545. (n) P.A. Evans, T.A. Brandt, Tetrahedron Lett. 37 (1996) 9143. (o) G.J. Dawson, J.M.J. Williams, Tetrahedron Lett. 36 (1995) 461. (p) I.C. Baldwin, J.M.J. Williams, R.P. Beskett, Tetrahedron Asymm. 6 (1995) 1515. (q) P. von Matt, O. Loiseleur, G. Koch, A. Pfaltz, C. Lefeber, T. Feucht, G. Helmchen, Tetrahedron Asymm. 5 (1994) 573. (r) P. von Matt, A. Pfaltz, Angew. Chem. Int. Ed. 32 (1993) 566.
    • (1995) Tetrahedron Asymm. , vol.6 , pp. 1515
    • Baldwin, I.C.1    Williams, J.M.J.2    Beskett, R.P.3
  • 34
    • 0028209777 scopus 로고
    • Some examples of phosphino-oxazoline use in catalysis: (a) X. Fang, M. Johannsen, S. Yao, N. Gathergood, R.G. Hazell, K.A. Jørgensen, J. Org. Chem. 64 (1999) 4844. (b) K. Selvakumar, M. Valentini, M. Worle, P.S. Pregosin, A. Albinati, Organometallics 18 (1999) 1207. (c) W. Zhang, Y.-I. Yoneda, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Asymm. 9 (1998) 3371. (d) Y. Nishibayashi, I. Takei, S. Uemura, M. Hidai, Organometallics 17 (1998) 3420. (e) B. Wiese, G. Helmchen, Tetrahedron Lett. 39 (1998) 5727. (f) R. Prétôt, A. Pfaltz, Angew. Chem. Int. Ed. 37 (1998) 323. (g) H.-J. Gais, H. Eichelmann, N. Spalthoff, F. Gerhards, M. Frank, G. Raabe, Tetrahedron Asymm. 8 (1998) 235. (h) A. Sudo, K. Saigo, J. Org. Chem. 62 (1997) 5508. (i) T. Sammakia, E.L. Stangeland, J. Org. Chem. 62 (1997) 6104. (j) K.H. Ahn, C.-W. Cho, J. Park, S. Lee, Tetrahedron Asymm. 8 (1997) 1179. (k) L. Ripa, A. Hallberg, J. Org. Chem. 62 (1997) 595. (l) Y. Nishibayashi, K. Segawa, H. Takada, K. Ohe, S. Uemura, Chem. Commun. (1996) 847. (m) W. Zhang, T. Hirao, I. Ikeda, Tetrahedron Lett. 37 (1996) 4545. (n) P.A. Evans, T.A. Brandt, Tetrahedron Lett. 37 (1996) 9143. (o) G.J. Dawson, J.M.J. Williams, Tetrahedron Lett. 36 (1995) 461. (p) I.C. Baldwin, J.M.J. Williams, R.P. Beskett, Tetrahedron Asymm. 6 (1995) 1515. (q) P. von Matt, O. Loiseleur, G. Koch, A. Pfaltz, C. Lefeber, T. Feucht, G. Helmchen, Tetrahedron Asymm. 5 (1994) 573. (r) P. von Matt, A. Pfaltz, Angew. Chem. Int. Ed. 32 (1993) 566.
    • (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
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    • 33748227479 scopus 로고
    • Some examples of phosphino-oxazoline use in catalysis: (a) X. Fang, M. Johannsen, S. Yao, N. Gathergood, R.G. Hazell, K.A. Jørgensen, J. Org. Chem. 64 (1999) 4844. (b) K. Selvakumar, M. Valentini, M. Worle, P.S. Pregosin, A. Albinati, Organometallics 18 (1999) 1207. (c) W. Zhang, Y.-I. Yoneda, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Asymm. 9 (1998) 3371. (d) Y. Nishibayashi, I. Takei, S. Uemura, M. Hidai, Organometallics 17 (1998) 3420. (e) B. Wiese, G. Helmchen, Tetrahedron Lett. 39 (1998) 5727. (f) R. Prétôt, A. Pfaltz, Angew. Chem. Int. Ed. 37 (1998) 323. (g) H.-J. Gais, H. Eichelmann, N. Spalthoff, F. Gerhards, M. Frank, G. Raabe, Tetrahedron Asymm. 8 (1998) 235. (h) A. Sudo, K. Saigo, J. Org. Chem. 62 (1997) 5508. (i) T. Sammakia, E.L. Stangeland, J. Org. Chem. 62 (1997) 6104. (j) K.H. Ahn, C.-W. Cho, J. Park, S. Lee, Tetrahedron Asymm. 8 (1997) 1179. (k) L. Ripa, A. Hallberg, J. Org. Chem. 62 (1997) 595. (l) Y. Nishibayashi, K. Segawa, H. Takada, K. Ohe, S. Uemura, Chem. Commun. (1996) 847. (m) W. Zhang, T. Hirao, I. Ikeda, Tetrahedron Lett. 37 (1996) 4545. (n) P.A. Evans, T.A. Brandt, Tetrahedron Lett. 37 (1996) 9143. (o) G.J. Dawson, J.M.J. Williams, Tetrahedron Lett. 36 (1995) 461. (p) I.C. Baldwin, J.M.J. Williams, R.P. Beskett, Tetrahedron Asymm. 6 (1995) 1515. (q) P. von Matt, O. Loiseleur, G. Koch, A. Pfaltz, C. Lefeber, T. Feucht, G. Helmchen, Tetrahedron Asymm. 5 (1994) 573. (r) P. von Matt, A. Pfaltz, Angew. Chem. Int. Ed. 32 (1993) 566.
    • (1993) Angew. Chem. Int. Ed. , vol.32 , pp. 566
    • Von Matt, P.1    Pfaltz, A.2
  • 36
    • 0033548253 scopus 로고    scopus 로고
    • Other heteroatom-functionalized oxazolines in catalysis: (a) G. Chelucci, S. Medici, A. Saba, Tetrahedron Asymm. 10 (1999) 543. (b) S. Kanemasa, Y. Oderaotoshi, J. Tanaka, E. Wada, J. Am. Chem. Soc. 120 (1998) 12355. (c) K. Boog-Wick, P.S. Pregosin, G. Trabesinger, Organometallics 17 (1998) 3254. (d) S.-L. You, Y.-G. Zhou, X.-L. Hou, L.-X. Dai, J. Chem. Soc. Chem. Commun. (1998) 2765. (e) K. Nordstrom, E. Macedo, C. Moberg, J. Org. Chem. 62 (1997) 1604. (f) D.L. Davies, J. Fawcett, S.A. Garratt, D.R. Russel, J. Chem. Soc. Chem. Commun. (1997) 1351. (g) T. Ichiyanagi, M. Shimizu, T. Fuzisawa, Tetrahedron 53 (1997) 9599. (h) T. Fuzisawa, T. Ichiyanagi, M. Shimizu, Tetrahedron Lett. 36 (1995) 5031.
    • (1999) Tetrahedron Asymm. , vol.10 , pp. 543
    • Chelucci, G.1    Medici, S.2    Saba, A.3
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    • 0032477318 scopus 로고    scopus 로고
    • Other heteroatom-functionalized oxazolines in catalysis: (a) G. Chelucci, S. Medici, A. Saba, Tetrahedron Asymm. 10 (1999) 543. (b) S. Kanemasa, Y. Oderaotoshi, J. Tanaka, E. Wada, J. Am. Chem. Soc. 120 (1998) 12355. (c) K. Boog-Wick, P.S. Pregosin, G. Trabesinger, Organometallics 17 (1998) 3254. (d) S.-L. You, Y.-G. Zhou, X.-L. Hou, L.-X. Dai, J. Chem. Soc. Chem. Commun. (1998) 2765. (e) K. Nordstrom, E. Macedo, C. Moberg, J. Org. Chem. 62 (1997) 1604. (f) D.L. Davies, J. Fawcett, S.A. Garratt, D.R. Russel, J. Chem. Soc. Chem. Commun. (1997) 1351. (g) T. Ichiyanagi, M. Shimizu, T. Fuzisawa, Tetrahedron 53 (1997) 9599. (h) T. Fuzisawa, T. Ichiyanagi, M. Shimizu, Tetrahedron Lett. 36 (1995) 5031.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 12355
    • Kanemasa, S.1    Oderaotoshi, Y.2    Tanaka, J.3    Wada, E.4
  • 38
    • 0001670942 scopus 로고    scopus 로고
    • Other heteroatom-functionalized oxazolines in catalysis: (a) G. Chelucci, S. Medici, A. Saba, Tetrahedron Asymm. 10 (1999) 543. (b) S. Kanemasa, Y. Oderaotoshi, J. Tanaka, E. Wada, J. Am. Chem. Soc. 120 (1998) 12355. (c) K. Boog-Wick, P.S. Pregosin, G. Trabesinger, Organometallics 17 (1998) 3254. (d) S.-L. You, Y.-G. Zhou, X.-L. Hou, L.-X. Dai, J. Chem. Soc. Chem. Commun. (1998) 2765. (e) K. Nordstrom, E. Macedo, C. Moberg, J. Org. Chem. 62 (1997) 1604. (f) D.L. Davies, J. Fawcett, S.A. Garratt, D.R. Russel, J. Chem. Soc. Chem. Commun. (1997) 1351. (g) T. Ichiyanagi, M. Shimizu, T. Fuzisawa, Tetrahedron 53 (1997) 9599. (h) T. Fuzisawa, T. Ichiyanagi, M. Shimizu, Tetrahedron Lett. 36 (1995) 5031.
    • (1998) Organometallics , vol.17 , pp. 3254
    • Boog-Wick, K.1    Pregosin, P.S.2    Trabesinger, G.3
  • 39
    • 0032556757 scopus 로고    scopus 로고
    • Other heteroatom-functionalized oxazolines in catalysis: (a) G. Chelucci, S. Medici, A. Saba, Tetrahedron Asymm. 10 (1999) 543. (b) S. Kanemasa, Y. Oderaotoshi, J. Tanaka, E. Wada, J. Am. Chem. Soc. 120 (1998) 12355. (c) K. Boog-Wick, P.S. Pregosin, G. Trabesinger, Organometallics 17 (1998) 3254. (d) S.-L. You, Y.-G. Zhou, X.-L. Hou, L.-X. Dai, J. Chem. Soc. Chem. Commun. (1998) 2765. (e) K. Nordstrom, E. Macedo, C. Moberg, J. Org. Chem. 62 (1997) 1604. (f) D.L. Davies, J. Fawcett, S.A. Garratt, D.R. Russel, J. Chem. Soc. Chem. Commun. (1997) 1351. (g) T. Ichiyanagi, M. Shimizu, T. Fuzisawa, Tetrahedron 53 (1997) 9599. (h) T. Fuzisawa, T. Ichiyanagi, M. Shimizu, Tetrahedron Lett. 36 (1995) 5031.
    • (1998) J. Chem. Soc. Chem. Commun. , pp. 2765
    • You, S.-L.1    Zhou, Y.-G.2    Hou, X.-L.3    Dai, L.-X.4
  • 40
    • 0001542678 scopus 로고    scopus 로고
    • Other heteroatom-functionalized oxazolines in catalysis: (a) G. Chelucci, S. Medici, A. Saba, Tetrahedron Asymm. 10 (1999) 543. (b) S. Kanemasa, Y. Oderaotoshi, J. Tanaka, E. Wada, J. Am. Chem. Soc. 120 (1998) 12355. (c) K. Boog-Wick, P.S. Pregosin, G. Trabesinger, Organometallics 17 (1998) 3254. (d) S.-L. You, Y.-G. Zhou, X.-L. Hou, L.-X. Dai, J. Chem. Soc. Chem. Commun. (1998) 2765. (e) K. Nordstrom, E. Macedo, C. Moberg, J. Org. Chem. 62 (1997) 1604. (f) D.L. Davies, J. Fawcett, S.A. Garratt, D.R. Russel, J. Chem. Soc. Chem. Commun. (1997) 1351. (g) T. Ichiyanagi, M. Shimizu, T. Fuzisawa, Tetrahedron 53 (1997) 9599. (h) T. Fuzisawa, T. Ichiyanagi, M. Shimizu, Tetrahedron Lett. 36 (1995) 5031.
    • (1997) J. Org. Chem. , vol.62 , pp. 1604
    • Nordstrom, K.1    Macedo, E.2    Moberg, C.3
  • 41
    • 0002496624 scopus 로고    scopus 로고
    • Other heteroatom-functionalized oxazolines in catalysis: (a) G. Chelucci, S. Medici, A. Saba, Tetrahedron Asymm. 10 (1999) 543. (b) S. Kanemasa, Y. Oderaotoshi, J. Tanaka, E. Wada, J. Am. Chem. Soc. 120 (1998) 12355. (c) K. Boog-Wick, P.S. Pregosin, G. Trabesinger, Organometallics 17 (1998) 3254. (d) S.-L. You, Y.-G. Zhou, X.-L. Hou, L.-X. Dai, J. Chem. Soc. Chem. Commun. (1998) 2765. (e) K. Nordstrom, E. Macedo, C. Moberg, J. Org. Chem. 62 (1997) 1604. (f) D.L. Davies, J. Fawcett, S.A. Garratt, D.R. Russel, J. Chem. Soc. Chem. Commun. (1997) 1351. (g) T. Ichiyanagi, M. Shimizu, T. Fuzisawa, Tetrahedron 53 (1997) 9599. (h) T. Fuzisawa, T. Ichiyanagi, M. Shimizu, Tetrahedron Lett. 36 (1995) 5031.
    • (1997) J. Chem. Soc. Chem. Commun. , pp. 1351
    • Davies, D.L.1    Fawcett, J.2    Garratt, S.A.3    Russel, D.R.4
  • 42
    • 0030744464 scopus 로고    scopus 로고
    • Other heteroatom-functionalized oxazolines in catalysis: (a) G. Chelucci, S. Medici, A. Saba, Tetrahedron Asymm. 10 (1999) 543. (b) S. Kanemasa, Y. Oderaotoshi, J. Tanaka, E. Wada, J. Am. Chem. Soc. 120 (1998) 12355. (c) K. Boog-Wick, P.S. Pregosin, G. Trabesinger, Organometallics 17 (1998) 3254. (d) S.-L. You, Y.-G. Zhou, X.-L. Hou, L.-X. Dai, J. Chem. Soc. Chem. Commun. (1998) 2765. (e) K. Nordstrom, E. Macedo, C. Moberg, J. Org. Chem. 62 (1997) 1604. (f) D.L. Davies, J. Fawcett, S.A. Garratt, D.R. Russel, J. Chem. Soc. Chem. Commun. (1997) 1351. (g) T. Ichiyanagi, M. Shimizu, T. Fuzisawa, Tetrahedron 53 (1997) 9599. (h) T. Fuzisawa, T. Ichiyanagi, M. Shimizu, Tetrahedron Lett. 36 (1995) 5031.
    • (1997) Tetrahedron , vol.53 , pp. 9599
    • Ichiyanagi, T.1    Shimizu, M.2    Fuzisawa, T.3
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