메뉴 건너뛰기




Volumn 81, Issue 1, 2008, Pages 60-75

Multimetallic bifunctional asymmetric catalysis based on proximity effect control

Author keywords

[No Author keywords available]

Indexed keywords

ASYMMETRIC CATALYSES; ASYMMETRIC CATALYSTS; BIFUNCTIONAL; CHIRAL LIGANDS; CONTROL CONCEPTS; CYANATION REACTIONS; DIRECT ALDOL REACTIONS; HIGH REACTIVITIES; KINETIC RESOLUTIONS; METALLIC COMPLEXES; MICHAEL REACTIONS; PROXIMITY EFFECTS; SCHIFF BASE; SYNERGISTIC EFFECTS;

EID: 48249148123     PISSN: 00092673     EISSN: 13480634     Source Type: Journal    
DOI: 10.1246/bcsj.81.60     Document Type: Article
Times cited : (98)

References (173)
  • 1
    • 34250645639 scopus 로고    scopus 로고
    • For general reviews, see; a, ed. by K. Mikami, M, Lautens, Wiley
    • For general reviews, see; a) New Frontiers in Asymmetric Catalysis, ed. by K. Mikami, M, Lautens, Wiley, 2007.
    • (2007) New Frontiers in Asymmetric Catalysis
  • 2
    • 0003445429 scopus 로고    scopus 로고
    • ed. by E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Springer, Berlin
    • b) Comprehensive Asymmetric Catalysis, ed. by E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Springer, Berlin, 1999;
    • (1999) Comprehensive Asymmetric Catalysis
  • 3
    • 28644442668 scopus 로고    scopus 로고
    • ed. by E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Springer, Berlin, for Supplement I
    • Comprehensive Asymmetric Catalysis, ed. by E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Springer, Berlin, 2003, for Supplement I.
    • (2003) Comprehensive Asymmetric Catalysis
  • 8
    • 17444395097 scopus 로고    scopus 로고
    • ed. by M. Shibasaki, Y. Yamamoto, Wiley VCH, New York
    • d) Multimetaltic Catalysis in Organic Synthesis, ed. by M. Shibasaki, Y. Yamamoto, Wiley VCH, New York, 2004.
    • (2004) Multimetaltic Catalysis in Organic Synthesis
  • 10
    • 6044269452 scopus 로고    scopus 로고
    • A recent reviews on bifunctional organo-catalysis: a P. I. Dalko, L. Moisan, Angew. Chem., Int. Ed. 2004, 43, 5138.
    • A recent reviews on bifunctional organo-catalysis: a) P. I. Dalko, L. Moisan, Angew. Chem., Int. Ed. 2004, 43, 5138.
  • 11
    • 58149297800 scopus 로고    scopus 로고
    • b) Acc. Chem. Res. 2004, 37, Issue 8.
    • (2004) Acc. Chem. Res , vol.37 , Issue.8
  • 18
    • 58149298235 scopus 로고    scopus 로고
    • Recent review on asymmetric catalysis using sterically and electronically modified BINOL derivatives: J. M. Brunei, Chem. Rev. 2005, 105, 857, and references therein
    • Recent review on asymmetric catalysis using sterically and electronically modified BINOL derivatives: J. M. Brunei, Chem. Rev. 2005, 105, 857, and references therein.
  • 24
    • 0036105811 scopus 로고    scopus 로고
    • For a review on direct catalytic asymmetric aldol reactions,see: B. Alcaide, P. Almendros, Eur. J. Org. Chem. 2002, 1595, see also reviews in Refs. 3, 4, and 9c.
    • For a review on direct catalytic asymmetric aldol reactions,see: B. Alcaide, P. Almendros, Eur. J. Org. Chem. 2002, 1595, see also reviews in Refs. 3, 4, and 9c.
  • 25
    • 0037016618 scopus 로고    scopus 로고
    • For general reviews on the catalytic enantioselective aldol reaction, see: a
    • For general reviews on the catalytic enantioselective aldol reaction, see: a) C. Palomo, M. Oiarbide, J. M. Garcia, Chem. Eur. J. 2002, 8, 36.
    • (2002) Chem. Eur. J , vol.8 , pp. 36
    • Palomo, C.1    Oiarbide, M.2    Garcia, J.M.3
  • 27
    • 11844259698 scopus 로고    scopus 로고
    • ed. by R. Mahrwald,Wiley-VCH
    • c) Modern Aldol Reactions, ed. by R. Mahrwald,Wiley-VCH, 2003.
    • (2003) Modern Aldol Reactions
  • 29
    • 0034823456 scopus 로고    scopus 로고
    • For related works using binuclear zinc complexes, see:, 3367, and references therein; For related works using organo-catalysts, see reviews in Refs. 4, 8, and 9
    • For related works using binuclear zinc complexes, see: B. M. Trost, H. Ito, E. R. Silcoff, J. Am. Chem. Soc. 2001, 123, 3367, and references therein; For related works using organo-catalysts, see reviews in Refs. 4, 8, and 9.
    • (2001) J. Am. Chem. Soc , vol.123
    • Trost, B.M.1    Ito, H.2    Silcoff, E.R.3
  • 31
    • 0034635561 scopus 로고    scopus 로고
    • Coldspray ionization mass spectrometry (CSI-MS) method enables the direct observation of labile species in solution phase: a) S. Sakamoto, M. Fujita, K. Kim, K. Yamaguchi, Tetrahedron 2000, 56, 955.
    • Coldspray ionization mass spectrometry (CSI-MS) method enables the direct observation of labile species in solution phase: a) S. Sakamoto, M. Fujita, K. Kim, K. Yamaguchi, Tetrahedron 2000, 56, 955.
  • 34
    • 0344064789 scopus 로고    scopus 로고
    • Review for stereoselective synthesis of tetrasubstituted carbon stereocenter: 1
    • Review for stereoselective synthesis of tetrasubstituted carbon stereocenter: 1. Denissova, L. Barriault, Tetrahedron 2003, 59, 10105.
    • (2003) Tetrahedron , vol.59 , pp. 10105
    • Denissova, L.B.1
  • 35
    • 0041738169 scopus 로고    scopus 로고
    • Reviews for catalytic asymmetric conjugate additions, see:a
    • Reviews for catalytic asymmetric conjugate additions, see:a) T. Hayashi, K. Yamasaki, Chem. Rev. 2003, 103, 2829.
    • (2003) Chem. Rev , vol.103 , pp. 2829
    • Hayashi, T.1    Yamasaki, K.2
  • 38
    • 0035126119 scopus 로고    scopus 로고
    • review for organocatalytic conjugate additions
    • d) N. Krause, A. Hoffmann-Roder, Synthesis 2001, 171. A review for organocatalytic conjugate additions:
    • (2001) Synthesis , vol.171 , Issue.A
    • Krause, N.1    Hoffmann-Roder, A.2
  • 43
    • 0037009019 scopus 로고    scopus 로고
    • For other examples using Af-acylpyrrole as an ester surrogate, see: a
    • For other examples using Af-acylpyrrole as an ester surrogate, see: a) D. A. Evans, G. Borg, K. A. Scheidt, Angew. Chem., Int. Ed. 2002, 41, 3188.
    • (2002) Angew. Chem., Int. Ed , vol.41 , pp. 3188
    • Evans, D.A.1    Borg, G.2    Scheidt, K.A.3
  • 52
    • 0034697199 scopus 로고    scopus 로고
    • For reviews on asymmetric synthesis of vicinal amino alcohols, see: a
    • For reviews on asymmetric synthesis of vicinal amino alcohols, see: a) S. C. Bergmeier, Tetrahedron 2000, 56, 2561.
    • (2000) Tetrahedron , vol.56 , pp. 2561
    • Bergmeier, S.C.1
  • 53
    • 0000763561 scopus 로고    scopus 로고
    • b) M. Reetz, Chem. Rev. 1999, 99, 1121.
    • (1999) Chem. Rev , vol.99 , pp. 1121
    • Reetz, M.1
  • 54
    • 10844266525 scopus 로고    scopus 로고
    • For general reviews on catalytic asymmetric Mannich-type reaction, see: a, ed. by E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Springer, Berlin, Chap. 29.5, p
    • For general reviews on catalytic asymmetric Mannich-type reaction, see: a) S. Kobayashi, M. Ueno, in Comprehensive Asymmetric Catalysis, ed. by E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Springer, Berlin, 2003, Suppl. 1, Chap. 29.5, p. 143.
    • (2003) Comprehensive Asymmetric Catalysis , Issue.SUPPL. 1 , pp. 143
    • Kobayashi, S.1    Ueno, M.2
  • 56
    • 30444441133 scopus 로고    scopus 로고
    • Recent reviews for direct catalytic asymmetric Mannich reaction: a M. M. B. Marques, Angew. Chem., Int. Ed. 2006, 45, 348.
    • Recent reviews for direct catalytic asymmetric Mannich reaction: a) M. M. B. Marques, Angew. Chem., Int. Ed. 2006, 45, 348.
  • 59
    • 20344364640 scopus 로고    scopus 로고
    • A review for the use of Dpp-imines in organic synthesis: S. M. Weinreb, R. K. Orr, Synthesis 2005, 1205.
    • A review for the use of Dpp-imines in organic synthesis: S. M. Weinreb, R. K. Orr, Synthesis 2005, 1205.
  • 60
    • 0037462104 scopus 로고    scopus 로고
    • 25S. Matsunaga, N. Kumagai, S. Harada, M. Shibasaki, J. Am. Chem. Soc. 2003, 125, 4712.
    • 25S. Matsunaga, N. Kumagai, S. Harada, M. Shibasaki, J. Am. Chem. Soc. 2003, 125, 4712.
  • 61
    • 0037438599 scopus 로고    scopus 로고
    • For closely related works using a binuclear zinc complex, see: a
    • For closely related works using a binuclear zinc complex, see: a) B. M. Trost, L. R. Terrell, J. Am. Chem. Soc. 2003, 725, 338.
    • (2003) J. Am. Chem. Soc , vol.725 , pp. 338
    • Trost, B.M.1    Terrell, L.R.2
  • 62
    • 33644937519 scopus 로고    scopus 로고
    • 2778, for related works using organo-catalysts, see reviews in Refs. 4 and 23
    • b) B. M. Trost, J. Jaratjaroonphong, V. Reutrakul, J. Am. Chem. Soc. 2006, 128, 2778, for related works using organo-catalysts, see reviews in Refs. 4 and 23.
    • (2006) J. Am. Chem. Soc , vol.128
    • Trost, B.M.1    Jaratjaroonphong, J.2    Reutrakul, V.3
  • 65
    • 0042739593 scopus 로고    scopus 로고
    • For related works using conformationally flexible ligands in asymmetric catalysis, see reviews: a
    • For related works using conformationally flexible ligands in asymmetric catalysis, see reviews: a) K. Mikami, M. Yamanaka, Chem. Rev. 2003, 103, 3369.
    • (2003) Chem. Rev , vol.103 , pp. 3369
    • Mikami, K.1    Yamanaka, M.2
  • 71
    • 0038298158 scopus 로고    scopus 로고
    • Recent selected examples in direct enantioselective aldol reactions using ester equivalent donors; a D. A. Evans, C. W. Downey, J. L. Hubbs, J. Am. Chem. Soc. 2003, 125, 8706
    • Recent selected examples in direct enantioselective aldol reactions using ester equivalent donors; a) D. A. Evans, C. W. Downey, J. L. Hubbs, J. Am. Chem. Soc. 2003, 125, 8706.
  • 75
    • 3843094836 scopus 로고    scopus 로고
    • With glycinate Schiff base: T. Ooi, M. Kameda, M. Taniguchi, K. Maruoka, J. Am. Chem. Soc. 2004, 126, 9685, and references therein
    • With glycinate Schiff base: T. Ooi, M. Kameda, M. Taniguchi, K. Maruoka, J. Am. Chem. Soc. 2004, 126, 9685, and references therein.
  • 82
    • 33947226642 scopus 로고    scopus 로고
    • For the synthesis and applications of Ph-substituted BINOL derivatives: H. Kawabata, K. Omura, T. Uchida, T. Katsuki, Chem, Asian J. 2007, 2, 248, and references therein.
    • For the synthesis and applications of Ph-substituted BINOL derivatives: H. Kawabata, K. Omura, T. Uchida, T. Katsuki, Chem, Asian J. 2007, 2, 248, and references therein.
  • 84
    • 33947157241 scopus 로고    scopus 로고
    • For an example of direct catalytic Mannich-type reaction with a-alkyl-substituted ester equivalent donor in racemic reaction, see: a S. Saito, T. Tsubogo, S. Kobayashi, Chem. Commun. 2007, 1236. See also, direct Mannich-type reactions using ester equivalent donors without α-alkyl substituent, racemic reaction:
    • For an example of direct catalytic Mannich-type reaction with a-alkyl-substituted ester equivalent donor in racemic reaction, see: a) S. Saito, T. Tsubogo, S. Kobayashi, Chem. Commun. 2007, 1236. See also, direct Mannich-type reactions using ester equivalent donors without α-alkyl substituent, racemic reaction:
  • 87
    • 84989540865 scopus 로고    scopus 로고
    • For utility of TCMK and carbinol: a E. J. Corey, J. O. Link,. J. Am. Chem. Soc. 1992, 114, 1906.
    • For utility of TCMK and carbinol: a) E. J. Corey, J. O. Link,. J. Am. Chem. Soc. 1992, 114, 1906.
  • 93
    • 0000210659 scopus 로고    scopus 로고
    • For systematic studies on the leaving ability of CCI3 group, see: a C. Zucco, C. F. Lima, M. C. Rezende, J. F. Vianna, F. Nome, J. Org. Chem. 1987, 52, 5356.
    • For systematic studies on the leaving ability of CCI3 group, see: a) C. Zucco, C. F. Lima, M. C. Rezende, J. F. Vianna, F. Nome, J. Org. Chem. 1987, 52, 5356.
  • 95
    • 0026442610 scopus 로고
    • For structural aspects of trichloromethyl ketones, see:c
    • For structural aspects of trichloromethyl ketones, see:c) E. J. Corey, J. O. Link, S. Sarshar, Y. Shao, Tetrahedron Lett. 1992, 33, 7103.
    • (1992) Tetrahedron Lett , vol.33 , pp. 7103
    • Corey, E.J.1    Link, J.O.2    Sarshar, S.3    Shao, Y.4
  • 96
    • 33746255430 scopus 로고    scopus 로고
    • Utility of trichloromethyl ketones 6 as donors was first investigated in racemic system: H. Morimoto, S. H. Wiedemann,A. Yamaguchi, S. Harada, Z. Chen, S. Matsunaga, M. Shibasaki, Angew. Chem., Int. Ed. 2006, 45, 3146.
    • Utility of trichloromethyl ketones 6 as donors was first investigated in racemic system: H. Morimoto, S. H. Wiedemann,A. Yamaguchi, S. Harada, Z. Chen, S. Matsunaga, M. Shibasaki, Angew. Chem., Int. Ed. 2006, 45, 3146.
  • 97
    • 0034705375 scopus 로고    scopus 로고
    • For recent reports of Favorskii rearrangement and related reactions of acyclic trihalomethyl ketones including trichloro methyl ketones under basic conditions, see: a S. Braverman, M. Cherkinsky, E. V. K. S. Kumar, H. E. Gottlieb, Tetrahedron 2000, 56, 4521
    • For recent reports of Favorskii rearrangement and related reactions of acyclic trihalomethyl ketones including trichloro methyl ketones under basic conditions, see: a) S. Braverman, M. Cherkinsky, E. V. K. S. Kumar, H. E. Gottlieb, Tetrahedron 2000, 56, 4521.
  • 100
    • 33746649502 scopus 로고    scopus 로고
    • For selected recent examples of iV-heteroarenesulfonyl imines in asymmetric synthesis: a A. S. Gonzalez, R. G. Arrayas, J. C. Carretero, Org. Lett. 2006, 8, 2977, and references therein,
    • For selected recent examples of iV-heteroarenesulfonyl imines in asymmetric synthesis: a) A. S. Gonzalez, R. G. Arrayas, J. C. Carretero, Org. Lett. 2006, 8, 2977, and references therein,
  • 105
    • 0036625262 scopus 로고    scopus 로고
    • 3 in organic synthesis: S. Kobayashi, M. Sugiura, H. Kitagawa, W. W.-L. Lam, Chem. Rev. 2002, 102, 2227.
    • 3 in organic synthesis: S. Kobayashi, M. Sugiura, H. Kitagawa, W. W.-L. Lam, Chem. Rev. 2002, 102, 2227.
  • 106
    • 0043240876 scopus 로고    scopus 로고
    • For utility of rare earth metal (RE) triflate and/or halide-pybox complexes as chiral Lewis acids, see a review: a) G. Desimoni, G. Faita, P. Quadrelli, Chem. Rev. 2003, 103, 3119.
    • For utility of rare earth metal (RE) triflate and/or halide-pybox complexes as chiral Lewis acids, see a review: a) G. Desimoni, G. Faita, P. Quadrelli, Chem. Rev. 2003, 103, 3119.
  • 107
    • 58149285848 scopus 로고    scopus 로고
    • 3 /pybox complex as a bifunctional catalyst to generate nucleophilic RE-cyanide species, see: c S. E. Schaus, E. N. Jacobsen, Org. Lett. 2000, 2, 1001.
    • 3 /pybox complex as a bifunctional catalyst to generate nucleophilic RE-cyanide species, see: c) S. E. Schaus, E. N. Jacobsen, Org. Lett. 2000, 2, 1001.
  • 109
    • 84945959007 scopus 로고    scopus 로고
    • For the initial use of rare earth metal alkoxide as a Brønsted base catalyst for C-C bond formations, see: H. Sasai, T. Suzuki, S. Arai, T. Aral, M. Shibasaki, J. Am. Chem. Soc. 1992, 114, 4418
    • For the initial use of rare earth metal alkoxide as a Brønsted base catalyst for C-C bond formations, see: H. Sasai, T. Suzuki, S. Arai, T. Aral, M. Shibasaki, .J. Am. Chem. Soc. 1992, 114, 4418.
  • 110
    • 58149299106 scopus 로고    scopus 로고
    • Trichloromethyl carbinols were stereoselectively converted into azetidine carboxylates. See
    • Trichloromethyl carbinols were stereoselectively converted into azetidine carboxylates. See, Ref. 42.
    • , vol.42
    • Ref1
  • 112
    • 85153004990 scopus 로고    scopus 로고
    • The structures of related heterobimetallic Cu-rare earth metal-Schiff base complexes were unequivocally determined byX-ray crystallographic analysis, see: a R. Koner, G.-H. Lee, Y. Wang, H.-H. Wei, S. Mohanta, Eur. J. Inorg. Chem. 2005, 1500
    • The structures of related heterobimetallic Cu-rare earth metal-Schiff base complexes were unequivocally determined byX-ray crystallographic analysis, see: a) R. Koner, G.-H. Lee, Y. Wang, H.-H. Wei, S. Mohanta, Eur. J. Inorg. Chem. 2005, 1500.
  • 113
    • 0026837644 scopus 로고    scopus 로고
    • C. Benelli, P. Guerriero, S. Tamburini, P. A. Vigato, Mater. Chem. Phys., 1992, 31, 137, and references therein. For related early studies on structural and magnetic properties, see also:
    • b) C. Benelli, P. Guerriero, S. Tamburini, P. A. Vigato, Mater. Chem. Phys., 1992, 31, 137, and references therein. For related early studies on structural and magnetic properties, see also:
  • 117
    • 0037424485 scopus 로고    scopus 로고
    • For related attempts to develop bifunctional asymmetric catalysts using heterobimetallic Schiff base complexes, see:a V. Annamalai, E. F. DiMauro, P. J. Carroll, M. C. Kozlowski, J. Org. Chem, 2003, 68, 1973, and references therein. See, also
    • For related attempts to develop bifunctional asymmetric catalysts using heterobimetallic Schiff base complexes, see:a) V. Annamalai, E. F. DiMauro, P. J. Carroll, M. C. Kozlowski, J. Org. Chem, 2003, 68, 1973, and references therein. See, also:
  • 120
    • 0037434136 scopus 로고    scopus 로고
    • A review of catalytic asymmetric nitro-Mannich reactions: B. Westermann, Angew. Chem., Int. Ed. 2003, 42, 151.
    • A review of catalytic asymmetric nitro-Mannich reactions: B. Westermann, Angew. Chem., Int. Ed. 2003, 42, 151.
  • 121
    • 12344267138 scopus 로고    scopus 로고
    • Highly anti-selective catalytic asymmetric nitro-Mannich reactions with thioureas: a T. P. Yoon, E. N. Jacobsen, Angew. Chem., Int. Ed. 2005, 44, 466.
    • Highly anti-selective catalytic asymmetric nitro-Mannich reactions with thioureas: a) T. P. Yoon, E. N. Jacobsen, Angew. Chem., Int. Ed. 2005, 44, 466.
  • 129
    • 0030788440 scopus 로고    scopus 로고
    • A review for early works: M. Shibasaki, H. Sasai, T. Arai, Angew. Chem., Int. Ed. Engl. 1997, 36, 1236.
    • A review for early works: M. Shibasaki, H. Sasai, T. Arai, Angew. Chem., Int. Ed. Engl. 1997, 36, 1236.
  • 135
    • 3042835317 scopus 로고    scopus 로고
    • Reviews for related chiral ligand mixing strategy: a
    • Reviews for related chiral ligand mixing strategy: a) K. Ding, H. Du, Y. Yuan, J. Long, Chem. Eur. J. 2004, 10, 2872.
    • (2004) Chem. Eur. J , vol.10 , pp. 2872
    • Ding, K.1    Du, H.2    Yuan, Y.3    Long, J.4
  • 137
    • 1942436903 scopus 로고    scopus 로고
    • * 8b: a A. I. Meyers, T. D. Nelson, H. Moorlag, D. J. Rawson, A. Meier, Tetrahedron 2004, 60, 4459, and references therein.
    • * 8b: a) A. I. Meyers, T. D. Nelson, H. Moorlag, D. J. Rawson, A. Meier, Tetrahedron 2004, 60, 4459, and references therein.
  • 138
    • 0008757162 scopus 로고    scopus 로고
    • and references therein. For other utility of bi-phenyldiols in asymmetric catalysis, see: b
    • For other utility of bi-phenyldiols in asymmetric catalysis, see: b) T. Harada, T. M. T. Tuyet, A. Oku, Org. Lett. 2000, 2, 1319, and references therein.
    • (2000) Org. Lett , vol.2 , pp. 1319
    • Harada, T.1    Tuyet, T.M.T.2    Oku, A.3
  • 141
    • 8444252168 scopus 로고    scopus 로고
    • For a recent review of the catalytic asymmetric nitroaldol reaction, see
    • For a recent review of the catalytic asymmetric nitroaldol reaction, see: C. Palomo, M. Oiarbide, A. Mielgo, Angew. Chem., Int. Ed. 2004, 43, 5442.
    • (2004) Angew. Chem., Int. Ed , vol.43 , pp. 5442
    • Palomo, C.1    Oiarbide, M.2    Mielgo, A.3
  • 142
    • 21344465658 scopus 로고    scopus 로고
    • A recent general review for non-enzymatic kinetic resolution: a E. Vedejs, M. Jure, Angew. Chem., Int. Ed. 2005, 44, 3974. For an elegant kinetic resolution of tertiary aldols via retro-aldol reaction with a catalytic antibody, see:
    • A recent general review for non-enzymatic kinetic resolution: a) E. Vedejs, M. Jure, Angew. Chem., Int. Ed. 2005, 44, 3974. For an elegant kinetic resolution of tertiary aldols via retro-aldol reaction with a catalytic antibody, see:
  • 144
  • 146
    • 4744353743 scopus 로고    scopus 로고
    • Ligand liability of related rare earth-alkali metal heterobimetallic complexes was reported, a L. Di Bari, M. Lelli, P. Salvadori, Chem. Eur. J. 2004, 10, 4594.
    • Ligand liability of related rare earth-alkali metal heterobimetallic complexes was reported, a) L. Di Bari, M. Lelli, P. Salvadori, Chem. Eur. J. 2004, 10, 4594.
  • 149
    • 16844374787 scopus 로고    scopus 로고
    • A review for combined acid catalysis including Lewis acid-assisted Lewis acid catalysis, see
    • A review for combined acid catalysis including Lewis acid-assisted Lewis acid catalysis, see: H. Yamamoto, K. Futatsugi, Angew. Chem., Int. Ed. 2005, 44, 1924.
    • (2005) Angew. Chem., Int. Ed , vol.44 , pp. 1924
    • Yamamoto, H.1    Futatsugi, K.2
  • 150
    • 14944358971 scopus 로고    scopus 로고
    • Review for azo-Michael reaction: a L.-W. Xu, C.-G. Xia, Eur. J. Org. Chem. 2005, 633. Selected examples of catalytic asymmetric aza-Michael reactions using alkoxylamines with enones:
    • Review for azo-Michael reaction: a) L.-W. Xu, C.-G. Xia, Eur. J. Org. Chem. 2005, 633. Selected examples of catalytic asymmetric aza-Michael reactions using alkoxylamines with enones:
  • 154
    • 33646689324 scopus 로고    scopus 로고
    • L. Falborg, K. A. J0rgensen, J. Chem. Soc, Perkin Trans. 1 1996, 2823.
    • e) L. Falborg, K. A. J0rgensen, J. Chem. Soc, Perkin Trans. 1 1996, 2823.
  • 157
    • 3242810683 scopus 로고    scopus 로고
    • For recent reviews on asymmetric cyanation reactions: a
    • For recent reviews on asymmetric cyanation reactions: a) J. M. Brunei, I. P. Holmes, Angew. Chem., Int. Ed. 2004, 43, 2752.
    • (2004) Angew. Chem., Int. Ed , vol.43 , pp. 2752
    • Brunei, J.M.1    Holmes, I.P.2
  • 159
    • 0034833715 scopus 로고    scopus 로고
    • For leading references of related one-pot catalytic asym metric cyanation-protection sequences, see: a
    • For leading references of related one-pot catalytic asym metric cyanation-protection sequences, see: a) S.-K. Tian, L. Deng, J. Am. Chem, Soc. 2001, 123, 6195.
    • (2001) J. Am. Chem, Soc , vol.123 , pp. 6195
    • Tian, S.-K.1    Deng, L.2
  • 163
    • 0032192283 scopus 로고    scopus 로고
    • For other reports on the effects of various achiral phos-phine oxide additives in chiral rare earth metal complexes, see: a K. Daikai, M. Kamaura, J. Inanaga, Tetrahedron Lett. 1998, 39, 7321
    • For other reports on the effects of various achiral phos-phine oxide additives in chiral rare earth metal complexes, see: a) K. Daikai, M. Kamaura, J. Inanaga, Tetrahedron Lett. 1998, 39, 7321.
  • 171
    • 32244442811 scopus 로고    scopus 로고
    • We have also reported other applications of the proximity-effect-control catalysis in racemic reactions using a cationic Bi complex. Intermolecular hydroamination of dienes and vinyl are-nes: a H. Qin, N. Yamagiwa, S. Matsunaga, M. Shibasaki, J Am. Chem. Soc. 2006, 128, 1611
    • We have also reported other applications of the proximity-effect-control catalysis in racemic reactions using a cationic Bi complex. Intermolecular hydroamination of dienes and vinyl are-nes: a) H. Qin, N. Yamagiwa, S. Matsunaga, M. Shibasaki, J Am. Chem. Soc. 2006, 128, 1611.
  • 172
    • 33846316356 scopus 로고    scopus 로고
    • Direct amination of allylic, propargylic, and benzylic alcohols
    • b) H. Qin, N. Yamagiwa, S. Matsunaga, M. Shibasaki, Chem. Asian J. 2007, 2, 150. Direct amination of allylic, propargylic, and benzylic alcohols:
    • (2007) Chem. Asian J , vol.2 , pp. 150
    • Qin, H.1    Yamagiwa, N.2    Matsunaga, S.3    Shibasaki, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.