메뉴 건너뛰기




Volumn 8, Issue 21, 2002, Pages 5033-5042

Dramatically synergetic effect of carboxylic acid additive on tridentate titanium catalyzed enantioselective hetero-Diels - Alder reaction: Additive acceleration and nonlinear effect

Author keywords

Asymmetric catalysis; Diels Alder reaction; Nonlinear effect; Titanates; Tridentate ligands

Indexed keywords

ACCELERATION; ALDEHYDES; CATALYSIS; CATALYSTS; TITANIUM;

EID: 0037021035     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/1521-3765(20021104)8:21<5033::AID-CHEM5033>3.0.CO;2-T     Document Type: Article
Times cited : (70)

References (87)
  • 7
    • 84985633316 scopus 로고
    • a) S. J. Danishefsky, M. P. Deninno, Angew. Chem. 1987, 99, 15-23; Angew. Chem. Int. Ed. Engl. 1987, 26, 15-23;
    • (1987) Angew. Chem. Int. Ed. Engl. , vol.26 , pp. 15-23
  • 8
    • 0001546043 scopus 로고    scopus 로고
    • b) K. A. Jorgensen, Angew. Chem. 2000. 112, 3702-3733; Angew. Chem. Int. Ed. 2000, 39, 3558-3588;
    • (2000) Angew. Chem. , vol.112 , pp. 3702-3733
    • Jorgensen, K.A.1
  • 9
    • 0034675619 scopus 로고    scopus 로고
    • b) K. A. Jorgensen, Angew. Chem. 2000. 112, 3702-3733; Angew. Chem. Int. Ed. 2000, 39, 3558-3588;
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 3558-3588
  • 10
    • 0011779578 scopus 로고    scopus 로고
    • (Ed.: I. Ojima), 2nd ed., Wiley-VCH, New York, Chapter 8A
    • c) K. Maruoka in Catalysis Asymmetric Synthesis (Ed.: I. Ojima), 2nd ed., Wiley-VCH, New York, 2000, Chapter SA.
    • (2000) Catalysis Asymmetric Synthesis
    • Maruoka, K.1
  • 16
    • 0000210159 scopus 로고
    • 8-BINOL-Ti catalyzed asymmetric HDA of Danishefsky's diene with aldehydes in the presence or absence of molecular sieves (MS), see: a) K. Mikami, Y. Motoyama, M. Terada, J. Am. Chem. Soc. 1994, 116, 2812-2820; b) G. E. Keck, X. Y. Li, D. Krishnamurthy, J. Org. Chem. 1995, 60, 5998-5999; c) B. Wang, X. Feng, X. Cui, H. Liu, Y. Jiang, Chem. Commun. 2000, 1605-1606; for our preliminary results, see: d) see: d) J. Long, J. Hu, X. Shen, B. Ji, K, Ding, J. Am. Chem. Soc. 2002, 124, 10-11.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 2812-2820
    • Mikami, K.1    Motoyama, Y.2    Terada, M.3
  • 17
    • 0028886765 scopus 로고
    • 8-BINOL-Ti catalyzed asymmetric HDA of Danishefsky's diene with aldehydes in the presence or absence of molecular sieves (MS), see: a) K. Mikami, Y. Motoyama, M. Terada, J. Am. Chem. Soc. 1994, 116, 2812-2820; b) G. E. Keck, X. Y. Li, D. Krishnamurthy, J. Org. Chem. 1995, 60, 5998-5999; c) B. Wang, X. Feng, X. Cui, H. Liu, Y. Jiang, Chem. Commun. 2000, 1605-1606; for our preliminary results, see: d) see: d) J. Long, J. Hu, X. Shen, B. Ji, K, Ding, J. Am. Chem. Soc. 2002, 124, 10-11.
    • (1995) J. Org. Chem. , vol.60 , pp. 5998-5999
    • Keck, G.E.1    Li, X.Y.2    Krishnamurthy, D.3
  • 18
    • 0034618693 scopus 로고    scopus 로고
    • 8-BINOL-Ti catalyzed asymmetric HDA of Danishefsky's diene with aldehydes in the presence or absence of molecular sieves (MS), see: a) K. Mikami, Y. Motoyama, M. Terada, J. Am. Chem. Soc. 1994, 116, 2812-2820; b) G. E. Keck, X. Y. Li, D. Krishnamurthy, J. Org. Chem. 1995, 60, 5998-5999; c) B. Wang, X. Feng, X. Cui, H. Liu, Y. Jiang, Chem. Commun. 2000, 1605-1606; for our preliminary results, see: d) see: d) J. Long, J. Hu, X. Shen, B. Ji, K, Ding, J. Am. Chem. Soc. 2002, 124, 10-11.
    • (2000) Chem. Commun. , pp. 1605-1606
    • Wang, B.1    Feng, X.2    Cui, X.3    Liu, H.4    Jiang, Y.5
  • 19
    • 0037045239 scopus 로고    scopus 로고
    • 8-BINOL-Ti catalyzed asymmetric HDA of Danishefsky's diene with aldehydes in the presence or absence of molecular sieves (MS), see: a) K. Mikami, Y. Motoyama, M. Terada, J. Am. Chem. Soc. 1994, 116, 2812-2820; b) G. E. Keck, X. Y. Li, D. Krishnamurthy, J. Org. Chem. 1995, 60, 5998-5999; c) B. Wang, X. Feng, X. Cui, H. Liu, Y. Jiang, Chem. Commun. 2000, 1605-1606; for our preliminary results, see: d) see: d) J. Long, J. Hu, X. Shen, B. Ji, K, Ding, J. Am. Chem. Soc. 2002, 124, 10-11.
    • (2002) J. Am. Chem. Soc. , vol.124 , pp. 10-11
    • Long, J.1    Hu, J.2    Shen, X.3    Ji, B.4    Ding, K.5
  • 22
    • 0033549737 scopus 로고    scopus 로고
    • b) A. G. Dossetter, T F. Jamison, E. N. Jacobsen, Angew. Chem. 1999, 111, 2549-2552; Angew. Chem. Int. Ed. 1999, 38, 2398-2400;
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 2398-2400
  • 28
    • 0037083878 scopus 로고    scopus 로고
    • c) P. I. Dalko, L. Moisan, J. Cossy, Angew. Chem. 2002, 114, 647-650; Angew. Chem. Int. Ed. 2002, 41, 625-628.
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 625-628
  • 36
    • 0001032612 scopus 로고    scopus 로고
    • d) X. Hu, H. Chen, X. Zhang, Angew. Chem. 1999, 111, 3720-3723; Angew. Chem. Int. Ed. 1999, 38, 3518-3521;
    • (1999) Angew. Chem. , vol.111 , pp. 3720-3723
    • Hu, X.1    Chen, H.2    Zhang, X.3
  • 37
    • 0033521217 scopus 로고    scopus 로고
    • d) X. Hu, H. Chen, X. Zhang, Angew. Chem. 1999, 111, 3720-3723; Angew. Chem. Int. Ed. 1999, 38, 3518-3521;
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 3518-3521
  • 45
    • 0035907042 scopus 로고    scopus 로고
    • k) Y. N. Belokon, K. A. Kochetkov, T. D. Churkina, N. S. Ikonnikov, O. V. Larionov, S. R. Harutyunyan, S. Vyskocil, M. North, H. B. Kagan, Angew. Chem. 2001, 113, 2002-2005; Angew. Chem. Int. Ed. 2001, 40, 1948-1951;
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 1948-1951
  • 54
    • 0033520302 scopus 로고    scopus 로고
    • a) B. Jandeleit, D. J. Schaefer, T. S. Powers, H. W. Turner, W. H. Weinberg, Angew. Chem. 1999, 111, 2648-2689; Angew. Chem. Int. Ed. 1999, 38, 2494-2532;
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 2494-2532
  • 57
    • 0000486957 scopus 로고    scopus 로고
    • d) M. T. Reetz, Angew. Chem. 2001, 113, 292-321; Angew. Chem. Int. Ed. 2001, 40, 284-310;
    • (2001) Angew. Chem. , vol.113 , pp. 292-321
    • Reetz, M.T.1
  • 58
    • 0035910597 scopus 로고    scopus 로고
    • d) M. T. Reetz, Angew. Chem. 2001, 113, 292-321; Angew. Chem. Int. Ed. 2001, 40, 284-310;
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 284-310
  • 62
    • 0031038136 scopus 로고    scopus 로고
    • For leading examples of asymmetric activation and chiral drugging, see: a) K. Mikami, S. Matsukawa, Nature 1997, 385, 613-615; b) T. Ohkuma, H. Doucet, T. Pham, K. Mikami, T. Korenaga, M. Terada, R. Noyori, J. Am. Chem. Soc. 1998, 120, 1086-1807; c) K. Mikami, T. Korenaga, M. Terada, T. Ohkuma, T. Pham, R. Noyori, Angew. Chem. 1999, 111, 517-519; Angew. Chem. Int. Ed. 1999, 38, 495-497; d) K. Ding, A. Ishii, K. Mikami, Angew. Chem. 1999, 111, 519-523; Angew. Chem. Int. Ed. 1999, 38, 497-501; e) A. Ishii, V. A. Soloshonok, K. Mikami, J. Org. Chem. 2000, 65, 1597-1501; for comprehensive review, see: f) K. Mikami, M. Terada, T. Korenaga, Y. Matsumoto, M. Ueki, R. Angelaud, Angew. Chem. 2000, 112, 3676-3701; Angew. Chem. Int. Ed. 2000, 39, 3532-3556.
    • (1997) Nature , vol.385 , pp. 613-615
    • Mikami, K.1    Matsukawa, S.2
  • 63
    • 0032506982 scopus 로고    scopus 로고
    • For leading examples of asymmetric activation and chiral drugging, see: a) K. Mikami, S. Matsukawa, Nature 1997, 385, 613-615; b) T. Ohkuma, H. Doucet, T. Pham, K. Mikami, T. Korenaga, M. Terada, R. Noyori, J. Am. Chem. Soc. 1998, 120, 1086-1807; c) K. Mikami, T. Korenaga, M. Terada, T. Ohkuma, T. Pham, R. Noyori, Angew. Chem. 1999, 111, 517-519; Angew. Chem. Int. Ed. 1999, 38, 495-497; d) K. Ding, A. Ishii, K. Mikami, Angew. Chem. 1999, 111, 519-523; Angew. Chem. Int. Ed. 1999, 38, 497-501; e) A. Ishii, V. A. Soloshonok, K. Mikami, J. Org. Chem. 2000, 65, 1597-1501; for comprehensive review, see: f) K. Mikami, M. Terada, T. Korenaga, Y. Matsumoto, M. Ueki, R. Angelaud, Angew. Chem. 2000, 112, 3676-3701; Angew. Chem. Int. Ed. 2000, 39, 3532-3556.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 1086-1807
    • Ohkuma, T.1    Doucet, H.2    Pham, T.3    Mikami, K.4    Korenaga, T.5    Terada, M.6    Noyori, R.7
  • 64
    • 0001712058 scopus 로고    scopus 로고
    • For leading examples of asymmetric activation and chiral drugging, see: a) K. Mikami, S. Matsukawa, Nature 1997, 385, 613-615; b) T. Ohkuma, H. Doucet, T. Pham, K. Mikami, T. Korenaga, M. Terada, R. Noyori, J. Am. Chem. Soc. 1998, 120, 1086-1807; c) K. Mikami, T. Korenaga, M. Terada, T. Ohkuma, T. Pham, R. Noyori, Angew. Chem. 1999, 111, 517-519; Angew. Chem. Int. Ed. 1999, 38, 495-497; d) K. Ding, A. Ishii, K. Mikami, Angew. Chem. 1999, 111, 519-523; Angew. Chem. Int. Ed. 1999, 38, 497-501; e) A. Ishii, V. A. Soloshonok, K. Mikami, J. Org. Chem. 2000, 65, 1597-1501; for comprehensive review, see: f) K. Mikami, M. Terada, T. Korenaga, Y. Matsumoto, M. Ueki, R. Angelaud, Angew. Chem. 2000, 112, 3676-3701; Angew. Chem. Int. Ed. 2000, 39, 3532-3556.
    • (1999) Angew. Chem. , vol.111 , pp. 517-519
    • Mikami, K.1    Korenaga, T.2    Terada, M.3    Ohkuma, T.4    Pham, T.5    Noyori, R.6
  • 65
    • 0033558168 scopus 로고    scopus 로고
    • For leading examples of asymmetric activation and chiral drugging, see: a) K. Mikami, S. Matsukawa, Nature 1997, 385, 613-615; b) T. Ohkuma, H. Doucet, T. Pham, K. Mikami, T. Korenaga, M. Terada, R. Noyori, J. Am. Chem. Soc. 1998, 120, 1086-1807; c) K. Mikami, T. Korenaga, M. Terada, T. Ohkuma, T. Pham, R. Noyori, Angew. Chem. 1999, 111, 517-519; Angew. Chem. Int. Ed. 1999, 38, 495-497; d) K. Ding, A. Ishii, K. Mikami, Angew. Chem. 1999, 111, 519-523; Angew. Chem. Int. Ed. 1999, 38, 497-501; e) A. Ishii, V. A. Soloshonok, K. Mikami, J. Org. Chem. 2000, 65, 1597-1501; for comprehensive review, see: f) K. Mikami, M. Terada, T. Korenaga, Y. Matsumoto, M. Ueki, R. Angelaud, Angew. Chem. 2000, 112, 3676-3701; Angew. Chem. Int. Ed. 2000, 39, 3532-3556.
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 495-497
  • 66
    • 0001704546 scopus 로고    scopus 로고
    • For leading examples of asymmetric activation and chiral drugging, see: a) K. Mikami, S. Matsukawa, Nature 1997, 385, 613-615; b) T. Ohkuma, H. Doucet, T. Pham, K. Mikami, T. Korenaga, M. Terada, R. Noyori, J. Am. Chem. Soc. 1998, 120, 1086-1807; c) K. Mikami, T. Korenaga, M. Terada, T. Ohkuma, T. Pham, R. Noyori, Angew. Chem. 1999, 111, 517-519; Angew. Chem. Int. Ed. 1999, 38, 495-497; d) K. Ding, A. Ishii, K. Mikami, Angew. Chem. 1999, 111, 519-523; Angew. Chem. Int. Ed. 1999, 38, 497-501; e) A. Ishii, V. A. Soloshonok, K. Mikami, J. Org. Chem. 2000, 65, 1597-1501; for comprehensive review, see: f) K. Mikami, M. Terada, T. Korenaga, Y. Matsumoto, M. Ueki, R. Angelaud, Angew. Chem. 2000, 112, 3676-3701; Angew. Chem. Int. Ed. 2000, 39, 3532-3556.
    • (1999) Angew. Chem. , vol.111 , pp. 519-523
    • Ding, K.1    Ishii, A.2    Mikami, K.3
  • 67
    • 0033557464 scopus 로고    scopus 로고
    • For leading examples of asymmetric activation and chiral drugging, see: a) K. Mikami, S. Matsukawa, Nature 1997, 385, 613-615; b) T. Ohkuma, H. Doucet, T. Pham, K. Mikami, T. Korenaga, M. Terada, R. Noyori, J. Am. Chem. Soc. 1998, 120, 1086-1807; c) K. Mikami, T. Korenaga, M. Terada, T. Ohkuma, T. Pham, R. Noyori, Angew. Chem. 1999, 111, 517-519; Angew. Chem. Int. Ed. 1999, 38, 495-497; d) K. Ding, A. Ishii, K. Mikami, Angew. Chem. 1999, 111, 519-523; Angew. Chem. Int. Ed. 1999, 38, 497-501; e) A. Ishii, V. A. Soloshonok, K. Mikami, J. Org. Chem. 2000, 65, 1597-1501; for comprehensive review, see: f) K. Mikami, M. Terada, T. Korenaga, Y. Matsumoto, M. Ueki, R. Angelaud, Angew. Chem. 2000, 112, 3676-3701; Angew. Chem. Int. Ed. 2000, 39, 3532-3556.
    • (1999) Angew. Chem. Int. Ed. , vol.38 , pp. 497-501
  • 68
    • 0034629361 scopus 로고    scopus 로고
    • For leading examples of asymmetric activation and chiral drugging, see: a) K. Mikami, S. Matsukawa, Nature 1997, 385, 613-615; b) T. Ohkuma, H. Doucet, T. Pham, K. Mikami, T. Korenaga, M. Terada, R. Noyori, J. Am. Chem. Soc. 1998, 120, 1086-1807; c) K. Mikami, T. Korenaga, M. Terada, T. Ohkuma, T. Pham, R. Noyori, Angew. Chem. 1999, 111, 517-519; Angew. Chem. Int. Ed. 1999, 38, 495-497; d) K. Ding, A. Ishii, K. Mikami, Angew. Chem. 1999, 111, 519-523; Angew. Chem. Int. Ed. 1999, 38, 497-501; e) A. Ishii, V. A. Soloshonok, K. Mikami, J. Org. Chem. 2000, 65, 1597-1501; for comprehensive review, see: f) K. Mikami, M. Terada, T. Korenaga, Y. Matsumoto, M. Ueki, R. Angelaud, Angew. Chem. 2000, 112, 3676-3701; Angew. Chem. Int. Ed. 2000, 39, 3532-3556.
    • (2000) J. Org. Chem. , vol.65 , pp. 1597-1501
    • Ishii, A.1    Soloshonok, V.A.2    Mikami, K.3
  • 69
    • 0001684888 scopus 로고    scopus 로고
    • For leading examples of asymmetric activation and chiral drugging, see: a) K. Mikami, S. Matsukawa, Nature 1997, 385, 613-615; b) T. Ohkuma, H. Doucet, T. Pham, K. Mikami, T. Korenaga, M. Terada, R. Noyori, J. Am. Chem. Soc. 1998, 120, 1086-1807; c) K. Mikami, T. Korenaga, M. Terada, T. Ohkuma, T. Pham, R. Noyori, Angew. Chem. 1999, 111, 517-519; Angew. Chem. Int. Ed. 1999, 38, 495-497; d) K. Ding, A. Ishii, K. Mikami, Angew. Chem. 1999, 111, 519-523; Angew. Chem. Int. Ed. 1999, 38, 497-501; e) A. Ishii, V. A. Soloshonok, K. Mikami, J. Org. Chem. 2000, 65, 1597-1501; for comprehensive review, see: f) K. Mikami, M. Terada, T. Korenaga, Y. Matsumoto, M. Ueki, R. Angelaud, Angew. Chem. 2000, 112, 3676-3701; Angew. Chem. Int. Ed. 2000, 39, 3532-3556.
    • (2000) Angew. Chem. , vol.112 , pp. 3676-3701
    • Mikami, K.1    Terada, M.2    Korenaga, T.3    Matsumoto, Y.4    Ueki, M.5    Angelaud, R.6
  • 70
    • 0034675555 scopus 로고    scopus 로고
    • For leading examples of asymmetric activation and chiral drugging, see: a) K. Mikami, S. Matsukawa, Nature 1997, 385, 613-615; b) T. Ohkuma, H. Doucet, T. Pham, K. Mikami, T. Korenaga, M. Terada, R. Noyori, J. Am. Chem. Soc. 1998, 120, 1086-1807; c) K. Mikami, T. Korenaga, M. Terada, T. Ohkuma, T. Pham, R. Noyori, Angew. Chem. 1999, 111, 517-519; Angew. Chem. Int. Ed. 1999, 38, 495-497; d) K. Ding, A. Ishii, K. Mikami, Angew. Chem. 1999, 111, 519-523; Angew. Chem. Int. Ed. 1999, 38, 497-501; e) A. Ishii, V. A. Soloshonok, K. Mikami, J. Org. Chem. 2000, 65, 1597-1501; for comprehensive review, see: f) K. Mikami, M. Terada, T. Korenaga, Y. Matsumoto, M. Ueki, R. Angelaud, Angew. Chem. 2000, 112, 3676-3701; Angew. Chem. Int. Ed. 2000, 39, 3532-3556.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 3532-3556
  • 71
    • 0000025972 scopus 로고    scopus 로고
    • For comprehensive reviews on NLE in asymmetric catalysis, see: a) D. R. Fenwick, H. B. Kagan, Top. Stereochem. 1999. 22. 257-296; b) C. Girard, H. B. Kagan, Angew. Chem. 1998, 110. 3088-3127; Angew. Chem. Int. Ed. 1998, 37, 2922-2959; c) C. Bolm in Advanced Asymmetric Catalysis (Ed.: G. R. Stephenson), Chapman & Hall, London. 1996, pp. 9-26; d) D. Heller, H.-J. Drexler, C. Fischer, H. Buschmann, W. Baumann, B. Heller, Angew. Chem. 2000, 112, 505-509; Angew. Chem. Int. Ed. 2000, 39, 495-499; e) M. Avalos, R. Babiano, P. Cintas, J. L. Jimenez, J. C. Palacios, Tetrahedron: Asymmetry 1997, 8, 2997-3017.
    • (1999) Top. Stereochem. , vol.22 , pp. 257-296
    • Fenwick, D.R.1    Kagan, H.B.2
  • 72
    • 0000655043 scopus 로고    scopus 로고
    • For comprehensive reviews on NLE in asymmetric catalysis, see: a) D. R. Fenwick, H. B. Kagan, Top. Stereochem. 1999. 22. 257-296; b) C. Girard, H. B. Kagan, Angew. Chem. 1998, 110. 3088-3127; Angew. Chem. Int. Ed. 1998, 37, 2922-2959; c) C. Bolm in Advanced Asymmetric Catalysis (Ed.: G. R. Stephenson), Chapman & Hall, London. 1996, pp. 9-26; d) D. Heller, H.-J. Drexler, C. Fischer, H. Buschmann, W. Baumann, B. Heller, Angew. Chem. 2000, 112, 505-509; Angew. Chem. Int. Ed. 2000, 39, 495-499; e) M. Avalos, R. Babiano, P. Cintas, J. L. Jimenez, J. C. Palacios, Tetrahedron: Asymmetry 1997, 8, 2997-3017.
    • (1998) Angew. Chem. , vol.110 , pp. 3088-3127
    • Girard, C.1    Kagan, H.B.2
  • 73
    • 0032538773 scopus 로고    scopus 로고
    • For comprehensive reviews on NLE in asymmetric catalysis, see: a) D. R. Fenwick, H. B. Kagan, Top. Stereochem. 1999. 22. 257-296; b) C. Girard, H. B. Kagan, Angew. Chem. 1998, 110. 3088-3127; Angew. Chem. Int. Ed. 1998, 37, 2922-2959; c) C. Bolm in Advanced Asymmetric Catalysis (Ed.: G. R. Stephenson), Chapman & Hall, London. 1996, pp. 9-26; d) D. Heller, H.-J. Drexler, C. Fischer, H. Buschmann, W. Baumann, B. Heller, Angew. Chem. 2000, 112, 505-509; Angew. Chem. Int. Ed. 2000, 39, 495-499; e) M. Avalos, R. Babiano, P. Cintas, J. L. Jimenez, J. C. Palacios, Tetrahedron: Asymmetry 1997, 8, 2997-3017.
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 2922-2959
  • 74
    • 0004743192 scopus 로고    scopus 로고
    • (Ed.: G. R. Stephenson), Chapman & Hall, London
    • For comprehensive reviews on NLE in asymmetric catalysis, see: a) D. R. Fenwick, H. B. Kagan, Top. Stereochem. 1999. 22. 257-296; b) C. Girard, H. B. Kagan, Angew. Chem. 1998, 110. 3088-3127; Angew. Chem. Int. Ed. 1998, 37, 2922-2959; c) C. Bolm in Advanced Asymmetric Catalysis (Ed.: G. R. Stephenson), Chapman & Hall, London. 1996, pp. 9-26; d) D. Heller, H.-J. Drexler, C. Fischer, H. Buschmann, W. Baumann, B. Heller, Angew. Chem. 2000, 112, 505-509; Angew. Chem. Int. Ed. 2000, 39, 495-499; e) M. Avalos, R. Babiano, P. Cintas, J. L. Jimenez, J. C. Palacios, Tetrahedron: Asymmetry 1997, 8, 2997-3017.
    • (1996) Advanced Asymmetric Catalysis , pp. 9-26
    • Bolm, C.1
  • 75
    • 0003175705 scopus 로고    scopus 로고
    • For comprehensive reviews on NLE in asymmetric catalysis, see: a) D. R. Fenwick, H. B. Kagan, Top. Stereochem. 1999. 22. 257-296; b) C. Girard, H. B. Kagan, Angew. Chem. 1998, 110. 3088-3127; Angew. Chem. Int. Ed. 1998, 37, 2922-2959; c) C. Bolm in Advanced Asymmetric Catalysis (Ed.: G. R. Stephenson), Chapman & Hall, London. 1996, pp. 9-26; d) D. Heller, H.-J. Drexler, C. Fischer, H. Buschmann, W. Baumann, B. Heller, Angew. Chem. 2000, 112, 505-509; Angew. Chem. Int. Ed. 2000, 39, 495-499; e) M. Avalos, R. Babiano, P. Cintas, J. L. Jimenez, J. C. Palacios, Tetrahedron: Asymmetry 1997, 8, 2997-3017.
    • (2000) Angew. Chem. , vol.112 , pp. 505-509
    • Heller, D.1    Drexler, H.-J.2    Fischer, C.3    Buschmann, H.4    Baumann, W.5    Heller, B.6
  • 76
    • 0034603008 scopus 로고    scopus 로고
    • For comprehensive reviews on NLE in asymmetric catalysis, see: a) D. R. Fenwick, H. B. Kagan, Top. Stereochem. 1999. 22. 257-296; b) C. Girard, H. B. Kagan, Angew. Chem. 1998, 110. 3088-3127; Angew. Chem. Int. Ed. 1998, 37, 2922-2959; c) C. Bolm in Advanced Asymmetric Catalysis (Ed.: G. R. Stephenson), Chapman & Hall, London. 1996, pp. 9-26; d) D. Heller, H.-J. Drexler, C. Fischer, H. Buschmann, W. Baumann, B. Heller, Angew. Chem. 2000, 112, 505-509; Angew. Chem. Int. Ed. 2000, 39, 495-499; e) M. Avalos, R. Babiano, P. Cintas, J. L. Jimenez, J. C. Palacios, Tetrahedron: Asymmetry 1997, 8, 2997-3017.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 495-499
  • 77
    • 0030884481 scopus 로고    scopus 로고
    • For comprehensive reviews on NLE in asymmetric catalysis, see: a) D. R. Fenwick, H. B. Kagan, Top. Stereochem. 1999. 22. 257-296; b) C. Girard, H. B. Kagan, Angew. Chem. 1998, 110. 3088-3127; Angew. Chem. Int. Ed. 1998, 37, 2922-2959; c) C. Bolm in Advanced Asymmetric Catalysis (Ed.: G. R. Stephenson), Chapman & Hall, London. 1996, pp. 9-26; d) D. Heller, H.-J. Drexler, C. Fischer, H. Buschmann, W. Baumann, B. Heller, Angew. Chem. 2000, 112, 505-509; Angew. Chem. Int. Ed. 2000, 39, 495-499; e) M. Avalos, R. Babiano, P. Cintas, J. L. Jimenez, J. C. Palacios, Tetrahedron: Asymmetry 1997, 8, 2997-3017.
    • (1997) Tetrahedron Asymmetry , vol.8 , pp. 2997-3017
    • Avalos, M.1    Babiano, R.2    Cintas, P.3    Jimenez, J.L.4    Palacios, J.C.5
  • 78
    • 2242436569 scopus 로고    scopus 로고
    • note
    • For Mukaiyama aldol mechanism, see refs. [5, 6a]. For [4 + 2] cycloaddition mechanism, see refs. [7a, 10a, b].
  • 79
    • 0000606019 scopus 로고    scopus 로고
    • For the first synthesis, isolation and crystal structure determination of tridentate imino-alkoxytitanium complexes, see: R. Fleischer. H. Wunderlich, M. Braun, Eur. J. Org. Chem. 1998, 1063-1070.
    • (1998) Eur. J. Org. Chem. , pp. 1063-1070
    • Fleischer, R.1    Wunderlich, H.2    Braun, M.3
  • 87
    • 2242474207 scopus 로고    scopus 로고
    • note
    • CCDC-179981 ((R)-L1), -179980 ((R)-L7), and -179979 ((R)-L12) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html (or from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB21EZ, UK; fax: (+44) 1223-336033: or deposit@ccdc.cam.uk); fax: (+44) 1223-336033: or deposit@ccdc.cam.uk).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.