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Volumn 41, Issue 19, 2002, Pages 3554-3572

"Asymmetric" catalysis by lanthanide complexes

Author keywords

Asymmetric catalysis; Coordination chemistry; Enantioselectivity; Lanthanides; Lewis acids

Indexed keywords

CHEMICAL BONDS; DISSOCIATION; LANTHANUM COMPOUNDS; SUBSTITUTION REACTIONS; SUBSTRATES;

EID: 0037020389     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/1521-3773(20021004)41:19<3554::aid-anie3554>3.0.co;2-p     Document Type: Review
Times cited : (220)

References (213)
  • 7
    • 0003491247 scopus 로고
    • (Eds.: B. M. Trost, I. Fleming, S. L. Schreiber), Pergamon, Oxford
    • g) H. B. Kagan in Comprehensive Organic Synthesis, Vol. 8, (Eds.: B. M. Trost, I. Fleming, S. L. Schreiber), Pergamon, Oxford, 1992;
    • (1992) Comprehensive Organic Synthesis, Vol. 8 , vol.8
    • Kagan, H.B.1
  • 13
    • 0001212447 scopus 로고    scopus 로고
    • Organolanthanoid chemistry: Synthesis, structure, catalysis
    • d) "Organolanthanoid Chemistry: Synthesis, Structure, Catalysis": Top. Curr. Chem. 1996, 179;
    • (1996) Top. Curr. Chem. , vol.179
  • 16
    • 0000421996 scopus 로고
    • (Eds.: B. M. Trost, I. Fleming), Pergamon, Oxford
    • b) T. Imamoto in Comprehensive Organic Synthesis, Vol. 1 (Eds.: B. M. Trost, I. Fleming), Pergamon, Oxford, 1991, pp. 231-250;
    • (1991) Comprehensive Organic Synthesis , vol.1 , pp. 231-250
    • Imamoto, T.1
  • 27
  • 35
    • 2142822618 scopus 로고
    • (Eds.: K. A. Gschneidner, L. Eyring, G.R. Choppin, Lander G.H.), Elsevier, Amsterdam, chap. 124
    • e) H. A. Eick in Handbook on the Physics and Chemistry of Rare Earths (Eds.: K. A. Gschneidner, L. Eyring, G. R. Choppin, G. H. Lander), Elsevier, Amsterdam, 1994, chap. 124.
    • (1994) Handbook on the Physics and Chemistry of Rare Earths
    • Eick, H.A.1
  • 45
    • 33751499216 scopus 로고
    • K. Mikami, M. Terada, T. Nakai, J. Org. Chem. 1991, 56, 5456-5459; Annual Meeting of the Chemical Society of Japan (Kyoto), 1986, abstract papers no. 3Y29, 3Y30.
    • (1991) J. Org. Chem. , vol.56 , pp. 5456-5459
    • Mikami, K.1    Terada, M.2    Nakai, T.3
  • 49
    • 0004042577 scopus 로고
    • (Ed.: D. Schinzer), Kluwer, Dordrecht, chap. 4
    • Reviews on chelation- and nonchelation-controlled reactions: a) C. Gennari in Selectivities in Lewis Acid Promoted Reactions (Ed.: D. Schinzer), Kluwer, Dordrecht, 1989, chap. 4; b) M. T. Reetz, Organotitanium Reagents in Organic Synthesis, Springer, Berlin, 1986, chap. 5; c) M. T. Reetz, Angew. Chem. 1984, 96, 542-555; Angew. Chem. Int. Ed. Engl. 1984, 23, 556-569.
    • (1989) Selectivities in Lewis Acid Promoted Reactions
    • Gennari, C.1
  • 50
    • 0003780608 scopus 로고
    • Springer, Berlin, chap. 5
    • Reviews on chelation- and nonchelation-controlled reactions: a) C. Gennari in Selectivities in Lewis Acid Promoted Reactions (Ed.: D. Schinzer), Kluwer, Dordrecht, 1989, chap. 4; b) M. T. Reetz, Organotitanium Reagents in Organic Synthesis, Springer, Berlin, 1986, chap. 5; c) M. T. Reetz, Angew. Chem. 1984, 96, 542-555; Angew. Chem. Int. Ed. Engl. 1984, 23, 556-569.
    • (1986) Organotitanium Reagents in Organic Synthesis
    • Reetz, M.T.1
  • 51
    • 0000730188 scopus 로고
    • Reviews on chelation- and nonchelation-controlled reactions: a) C. Gennari in Selectivities in Lewis Acid Promoted Reactions (Ed.: D. Schinzer), Kluwer, Dordrecht, 1989, chap. 4; b) M. T. Reetz, Organotitanium Reagents in Organic Synthesis, Springer, Berlin, 1986, chap. 5; c) M. T. Reetz, Angew. Chem. 1984, 96, 542-555; Angew. Chem. Int. Ed. Engl. 1984, 23, 556-569.
    • (1984) Angew. Chem. , vol.96 , pp. 542-555
    • Reetz, M.T.1
  • 52
    • 0010771837 scopus 로고
    • Reviews on chelation- and nonchelation-controlled reactions: a) C. Gennari in Selectivities in Lewis Acid Promoted Reactions (Ed.: D. Schinzer), Kluwer, Dordrecht, 1989, chap. 4; b) M. T. Reetz, Organotitanium Reagents in Organic Synthesis, Springer, Berlin, 1986, chap. 5; c) M. T. Reetz, Angew. Chem. 1984, 96, 542-555; Angew. Chem. Int. Ed. Engl. 1984, 23, 556-569.
    • (1984) Angew. Chem. Int. Ed. Engl. , vol.23 , pp. 556-569
  • 64
    • 0030788440 scopus 로고    scopus 로고
    • M. Shibasaki, H. Sasai, T. Arai, Angew. Chem. 1997, 109, 1290-1310; Angew, Chem. Int. Ed. Engl. 1997, 36, 1236-1256.
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 1236-1256
  • 66
    • 0030863510 scopus 로고    scopus 로고
    • a) Y. M. A. Yamada, N. Yoshikawa, H. Sasai, M. Shibasaki, Angew. Chem. 1997, 109, 1942-1944; Angew. Chem. Int. Ed. Engl. 1997, 36, 1871-1873;
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 1871-1873
  • 81
    • 0007795046 scopus 로고
    • US Patent 3615169, 1971
    • a) K. F. Thom, US Patent 3615169, 1971 [Chem. Abstr. 1972, 76, 5436a];
    • (1972) Chem. Abstr. , vol.76
    • Thom, K.F.1
  • 89
    • 0030573985 scopus 로고    scopus 로고
    • These complexes also catalyzed the asymmetric aza-Diels-Alder reaction and 1,3-dipolar cycloadditions of nitrones with alkenes: a) H. Ishitani, S. Kobayashi, Tetrahedron Lett. 1996, 37, 7357-7360; b) S. Kobayashi, M. Kawamura, J. Am. Chem. Soc. 1998, 120, 5840-5841.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 7357-7360
    • Ishitani, H.1    Kobayashi, S.2
  • 90
    • 0032540703 scopus 로고    scopus 로고
    • These complexes also catalyzed the asymmetric aza-Diels-Alder reaction and 1,3-dipolar cycloadditions of nitrones with alkenes: a) H. Ishitani, S. Kobayashi, Tetrahedron Lett. 1996, 37, 7357-7360; b) S. Kobayashi, M. Kawamura, J. Am. Chem. Soc. 1998, 120, 5840-5841.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 5840-5841
    • Kobayashi, S.1    Kawamura, M.2
  • 101
  • 102
    • 0000609674 scopus 로고    scopus 로고
    • b) D. P. Curran, Angew. Chem. 1998, 110, 1230-1255; Angew. Chem. Int. Ed. 1998, 37, 1174-1196;
    • (1998) Angew. Chem. , vol.110 , pp. 1230-1255
    • Curran, D.P.1
  • 103
    • 0032543080 scopus 로고    scopus 로고
    • b) D. P. Curran, Angew. Chem. 1998, 110, 1230-1255; Angew. Chem. Int. Ed. 1998, 37, 1174-1196;
    • (1998) Angew. Chem. Int. Ed. , vol.37 , pp. 1174-1196
  • 105
    • 0000453314 scopus 로고    scopus 로고
    • d) B. Cornils, Angew. Chem. 1997, 109, 2147-2149; Angew. Chem. Int. Ed. Engl. 1997, 36, 2057-2059.
    • (1997) Angew. Chem. , vol.109 , pp. 2147-2149
    • Cornils, B.1
  • 106
    • 0030772233 scopus 로고    scopus 로고
    • d) B. Cornils, Angew. Chem. 1997, 109, 2147-2149; Angew. Chem. Int. Ed. Engl. 1997, 36, 2057-2059.
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 2057-2059
  • 110
    • 0001335865 scopus 로고
    • d) "Asymmetric Lewis Acid Catalysts": K. Mikami, T. Nakai, Kagaku Zoukan 1995, 124, 177-192;
    • (1995) Kagaku Zoukan , vol.124 , pp. 177-192
    • Mikami, K.1    Nakai, T.2
  • 118
    • 0034605820 scopus 로고    scopus 로고
    • Recent example of a fluorous binol-Ti catalyst: a) Y. Nakamura, S. Takeuchi, Y. Ohgo, D. P. Curran, Tetrahedron Lett. 2000, 41, 57-60; Y. Tian, K. S. Chan, Tetrahedron Lett. 2000, 41, 8813-8816.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 8813-8816
    • Tian, Y.1    Chan, K.S.2
  • 126
    • 0001704941 scopus 로고
    • Diastereofacial selective hetero-Diels-Alder reactions, catalyzed by achiral (or chiral) lanthanide complexes: a) M. M. Midland, R. S. Graham, J. Am. Chem. Soc. 1984, 106, 4294-4296; b) b) M. M. Midland, M. M. Afonso, J. Am. Chem. Soc. 1989, 111, 4368-4371; c) M. M. Midland, R. W. Koops, J. Org. Chem. 1990, 55, 5058-5065; d) C. Spino, G. Liu, J. Org. Chem. 1993, 58, 817-819; e) I. E. Marko, G. R. Evans, Tetrahedron Lett. 1994, 35, 2767-2770; f) I. E. Marko. G. R. Evans. Tetrahedron Lett. 1994, 35, 2771-2774; g) I. E. Marko. G. R. Evans, P. Seres, I. Chelle, Z. Janousek, Pure Appl. Chem. 1996, 68, 113-122.
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 4294-4296
    • Midland, M.M.1    Graham, R.S.2
  • 127
    • 0001578111 scopus 로고
    • Diastereofacial selective hetero-Diels-Alder reactions, catalyzed by achiral (or chiral) lanthanide complexes: a) M. M. Midland, R. S. Graham, J. Am. Chem. Soc. 1984, 106, 4294-4296; b) b) M. M. Midland, M. M. Afonso, J. Am. Chem. Soc. 1989, 111, 4368-4371; c) M. M. Midland, R. W. Koops, J. Org. Chem. 1990, 55, 5058-5065; d) C. Spino, G. Liu, J. Org. Chem. 1993, 58, 817-819; e) I. E. Marko, G. R. Evans, Tetrahedron Lett. 1994, 35, 2767-2770; f) I. E. Marko. G. R. Evans. Tetrahedron Lett. 1994, 35, 2771-2774; g) I. E. Marko. G. R. Evans, P. Seres, I. Chelle, Z. Janousek, Pure Appl. Chem. 1996, 68, 113-122.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 4368-4371
    • Midland, M.M.1    Afonso, M.M.2
  • 128
    • 33751553123 scopus 로고
    • Diastereofacial selective hetero-Diels-Alder reactions, catalyzed by achiral (or chiral) lanthanide complexes: a) M. M. Midland, R. S. Graham, J. Am. Chem. Soc. 1984, 106, 4294-4296; b) b) M. M. Midland, M. M. Afonso, J. Am. Chem. Soc. 1989, 111, 4368-4371; c) M. M. Midland, R. W. Koops, J. Org. Chem. 1990, 55, 5058-5065; d) C. Spino, G. Liu, J. Org. Chem. 1993, 58, 817-819; e) I. E. Marko, G. R. Evans, Tetrahedron Lett. 1994, 35, 2767-2770; f) I. E. Marko. G. R. Evans. Tetrahedron Lett. 1994, 35, 2771-2774; g) I. E. Marko. G. R. Evans, P. Seres, I. Chelle, Z. Janousek, Pure Appl. Chem. 1996, 68, 113-122.
    • (1990) J. Org. Chem. , vol.55 , pp. 5058-5065
    • Midland, M.M.1    Koops, R.W.2
  • 129
    • 0027466115 scopus 로고
    • Diastereofacial selective hetero-Diels-Alder reactions, catalyzed by achiral (or chiral) lanthanide complexes: a) M. M. Midland, R. S. Graham, J. Am. Chem. Soc. 1984, 106, 4294-4296; b) b) M. M. Midland, M. M. Afonso, J. Am. Chem. Soc. 1989, 111, 4368-4371; c) M. M. Midland, R. W. Koops, J. Org. Chem. 1990, 55, 5058-5065; d) C. Spino, G. Liu, J. Org. Chem. 1993, 58, 817-819; e) I. E. Marko, G. R. Evans, Tetrahedron Lett. 1994, 35, 2767-2770; f) I. E. Marko. G. R. Evans. Tetrahedron Lett. 1994, 35, 2771-2774; g) I. E. Marko. G. R. Evans, P. Seres, I. Chelle, Z. Janousek, Pure Appl. Chem. 1996, 68, 113-122.
    • (1993) J. Org. Chem. , vol.58 , pp. 817-819
    • Spino, C.1    Liu, G.2
  • 130
    • 0028226655 scopus 로고
    • Diastereofacial selective hetero-Diels-Alder reactions, catalyzed by achiral (or chiral) lanthanide complexes: a) M. M. Midland, R. S. Graham, J. Am. Chem. Soc. 1984, 106, 4294-4296; b) b) M. M. Midland, M. M. Afonso, J. Am. Chem. Soc. 1989, 111, 4368-4371; c) M. M. Midland, R. W. Koops, J. Org. Chem. 1990, 55, 5058-5065; d) C. Spino, G. Liu, J. Org. Chem. 1993, 58, 817-819; e) I. E. Marko, G. R. Evans, Tetrahedron Lett. 1994, 35, 2767-2770; f) I. E. Marko. G. R. Evans. Tetrahedron Lett. 1994, 35, 2771-2774; g) I. E. Marko. G. R. Evans, P. Seres, I. Chelle, Z. Janousek, Pure Appl. Chem. 1996, 68, 113-122.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 2767-2770
    • Marko, I.E.1    Evans, G.R.2
  • 131
    • 0028217046 scopus 로고
    • Diastereofacial selective hetero-Diels-Alder reactions, catalyzed by achiral (or chiral) lanthanide complexes: a) M. M. Midland, R. S. Graham, J. Am. Chem. Soc. 1984, 106, 4294-4296; b) b) M. M. Midland, M. M. Afonso, J. Am. Chem. Soc. 1989, 111, 4368-4371; c) M. M. Midland, R. W. Koops, J. Org. Chem. 1990, 55, 5058-5065; d) C. Spino, G. Liu, J. Org. Chem. 1993, 58, 817-819; e) I. E. Marko, G. R. Evans, Tetrahedron Lett. 1994, 35, 2767-2770; f) I. E. Marko. G. R. Evans. Tetrahedron Lett. 1994, 35, 2771-2774; g) I. E. Marko. G. R. Evans, P. Seres, I. Chelle, Z. Janousek, Pure Appl. Chem. 1996, 68, 113-122.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 2771-2774
    • Marko, I.E.1    Evans, G.R.2
  • 132
    • 0002126695 scopus 로고    scopus 로고
    • Diastereofacial selective hetero-Diels-Alder reactions, catalyzed by achiral (or chiral) lanthanide complexes: a) M. M. Midland, R. S. Graham, J. Am. Chem. Soc. 1984, 106, 4294-4296; b) b) M. M. Midland, M. M. Afonso, J. Am. Chem. Soc. 1989, 111, 4368-4371; c) M. M. Midland, R. W. Koops, J. Org. Chem. 1990, 55, 5058-5065; d) C. Spino, G. Liu, J. Org. Chem. 1993, 58, 817-819; e) I. E. Marko, G. R. Evans, Tetrahedron Lett. 1994, 35, 2767-2770; f) I. E. Marko. G. R. Evans. Tetrahedron Lett. 1994, 35, 2771-2774; g) I. E. Marko. G. R. Evans, P. Seres, I. Chelle, Z. Janousek, Pure Appl. Chem. 1996, 68, 113-122.
    • (1996) Pure Appl. Chem. , vol.68 , pp. 113-122
    • Marko, I.E.1    Evans, G.R.2    Seres, P.3    Chelle, I.4    Janousek, Z.5
  • 134
    • 2142643479 scopus 로고    scopus 로고
    • Masters Thesis, Tokyo Institute of Technology
    • b) O. Kotera, Masters Thesis, Tokyo Institute of Technology, 1997.
    • (1997)
    • Kotera, O.1
  • 139
    • 0030730058 scopus 로고    scopus 로고
    • Further asymmetric reactions catalyzed by Ln-pybox complexes: a) A. I. Sanchez-Blanco, K. V. Gothelf. K. A. Jørgensen, Tetrahedron Lett. 1997, 38, 7923-7926: b) H. C. Aspinall, N. Greeves, P. M. Smith, Tetrahedron Lett. 1999, 40, 1763; c) S. E. Schaus, E. N. Jacobsen, Org. Lett. 2000, 2, 1001-1004; d) C. Qian, L. Wang, Tetrahedron: Asymmetry 2000, 11, 2347-2357; e) S. Fukuzawa, H. Matsuzawa, K. Metoki, Synlett 2001, 709-711.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 7923-7926
    • Sanchez-Blanco, A.I.1    Gothelf, K.V.2    Jørgensen, K.A.3
  • 140
    • 0033605355 scopus 로고    scopus 로고
    • Further asymmetric reactions catalyzed by Ln-pybox complexes: a) A. I. Sanchez-Blanco, K. V. Gothelf. K. A. Jørgensen, Tetrahedron Lett. 1997, 38, 7923-7926: b) H. C. Aspinall, N. Greeves, P. M. Smith, Tetrahedron Lett. 1999, 40, 1763; c) S. E. Schaus, E. N. Jacobsen, Org. Lett. 2000, 2, 1001-1004; d) C. Qian, L. Wang, Tetrahedron: Asymmetry 2000, 11, 2347-2357; e) S. Fukuzawa, H. Matsuzawa, K. Metoki, Synlett 2001, 709-711.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 1763
    • Aspinall, H.C.1    Greeves, N.2    Smith, P.M.3
  • 141
    • 0034611489 scopus 로고    scopus 로고
    • Further asymmetric reactions catalyzed by Ln-pybox complexes: a) A. I. Sanchez-Blanco, K. V. Gothelf. K. A. Jørgensen, Tetrahedron Lett. 1997, 38, 7923-7926: b) H. C. Aspinall, N. Greeves, P. M. Smith, Tetrahedron Lett. 1999, 40, 1763; c) S. E. Schaus, E. N. Jacobsen, Org. Lett. 2000, 2, 1001-1004; d) C. Qian, L. Wang, Tetrahedron: Asymmetry 2000, 11, 2347-2357; e) S. Fukuzawa, H. Matsuzawa, K. Metoki, Synlett 2001, 709-711.
    • (2000) Org. Lett. , vol.2 , pp. 1001-1004
    • Schaus, S.E.1    Jacobsen, E.N.2
  • 142
    • 0034674549 scopus 로고    scopus 로고
    • Further asymmetric reactions catalyzed by Ln-pybox complexes: a) A. I. Sanchez-Blanco, K. V. Gothelf. K. A. Jørgensen, Tetrahedron Lett. 1997, 38, 7923-7926: b) H. C. Aspinall, N. Greeves, P. M. Smith, Tetrahedron Lett. 1999, 40, 1763; c) S. E. Schaus, E. N. Jacobsen, Org. Lett. 2000, 2, 1001-1004; d) C. Qian, L. Wang, Tetrahedron: Asymmetry 2000, 11, 2347-2357; e) S. Fukuzawa, H. Matsuzawa, K. Metoki, Synlett 2001, 709-711.
    • (2000) Tetrahedron: Asymmetry , vol.11 , pp. 2347-2357
    • Qian, C.1    Wang, L.2
  • 143
    • 0035032715 scopus 로고    scopus 로고
    • Further asymmetric reactions catalyzed by Ln-pybox complexes: a) A. I. Sanchez-Blanco, K. V. Gothelf. K. A. Jørgensen, Tetrahedron Lett. 1997, 38, 7923-7926: b) H. C. Aspinall, N. Greeves, P. M. Smith, Tetrahedron Lett. 1999, 40, 1763; c) S. E. Schaus, E. N. Jacobsen, Org. Lett. 2000, 2, 1001-1004; d) C. Qian, L. Wang, Tetrahedron: Asymmetry 2000, 11, 2347-2357; e) S. Fukuzawa, H. Matsuzawa, K. Metoki, Synlett 2001, 709-711.
    • (2001) Synlett , pp. 709-711
    • Fukuzawa, S.1    Matsuzawa, H.2    Metoki, K.3
  • 149
    • 85007750006 scopus 로고
    • Reviews: J. Inanaga, J. Synth. Org. Chem. Jpn. 1989, 47, 200-211; J. Inanaga, J. Synth. Org. Chem. Jpn. 1990, 48, 1024-1025.
    • (1989) J. Synth. Org. Chem. Jpn. , vol.47 , pp. 200-211
    • Inanaga, J.1
  • 150
    • 0010419814 scopus 로고
    • Reviews: J. Inanaga, J. Synth. Org. Chem. Jpn. 1989, 47, 200-211; J. Inanaga, J. Synth. Org. Chem. Jpn. 1990, 48, 1024-1025.
    • (1990) J. Synth. Org. Chem. Jpn. , vol.48 , pp. 1024-1025
    • Inanaga, J.1
  • 152
    • 0003913629 scopus 로고    scopus 로고
    • (Ed.: J. Otera), Wiley-VCH, Weinheim, chap. 3
    • a) G. C. Fu in Modern Carbonyl Chemistry (Ed.: J. Otera), Wiley-VCH. Weinheim, 2000, chap. 3;
    • (2000) Modern Carbonyl Chemistry
    • Fu, G.C.1
  • 153
    • 0002704057 scopus 로고
    • (Eds.: B. M. Trost, I. Fleming, G. Pattenden), Pergamon, New York
    • b) G. M. Robertson in Comprehensive Organic Synthesis, Vol. 3 (Eds.: B. M. Trost, I. Fleming, G. Pattenden), Pergamon, New York, 1991, pp. 613-632;
    • (1991) Comprehensive Organic Synthesis, Vol. 3 , vol.3 , pp. 613-632
    • Robertson, G.M.1
  • 156
    • 0002338708 scopus 로고    scopus 로고
    • e) T. Wirth, Angew. Chem. 1996, 108, 65-67; Angew. Chem. Int. Ed. Engl. 1996, 35, 61-63.
    • (1996) Angew. Chem. , vol.108 , pp. 65-67
    • Wirth, T.1
  • 157
    • 0003182150 scopus 로고    scopus 로고
    • e) T. Wirth, Angew. Chem. 1996, 108, 65-67; Angew. Chem. Int. Ed. Engl. 1996, 35, 61-63.
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 61-63
  • 175
    • 0010339556 scopus 로고    scopus 로고
    • Daitoinnsatsu, Osaka
    • Kagan and Inanaga examined a similar reaction, using a prolinol-derived phosphoramide and sparteine, respectively: J. Inanaga, New Development of Studies on Rare Earth Complexes, Daitoinnsatsu, Osaka, 1997, p. 263.
    • (1997) New Development of Studies on Rare Earth Complexes , pp. 263
    • Inanaga, J.1
  • 183
    • 0001231250 scopus 로고    scopus 로고
    • b) K. Mikami, A. Yoshida, Angew. Chem. 1997, 109, 892-894; Angew. Chem. Int. Ed. Engl. 1997, 36, 858-860.
    • (1997) Angew. Chem. , vol.109 , pp. 892-894
    • Mikami, K.1    Yoshida, A.2
  • 184
    • 0030968142 scopus 로고    scopus 로고
    • b) K. Mikami, A. Yoshida, Angew. Chem. 1997, 109, 892-894; Angew. Chem. Int. Ed. Engl. 1997, 36, 858-860.
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 858-860
  • 188
    • 0001084079 scopus 로고
    • Reviews on asymmetric protonation using chiral proton sources: a) L. Duhamel. P. Duhamel, J.-C. Launay, J.-C. Plaquevent, Bull. Soc. Chim. Fr. 1984, 421-430; b) S. Hunig in Methods Org. Chem. (Houben-Weyl) 4th ed. 1952-, Vol. E21, 1995, pp. 3851-3911: c) C. Fehr, Angew. Chem. 1996, 108, 2726-2748; Angew. Chem. Int. Ed. Engl. 1996, 35, 2566-2587.
    • (1984) Bull. Soc. Chim. Fr. , pp. 421-430
    • Duhamel, L.1    Duhamel, P.2    Launay, J.-C.3    Plaquevent, J.-C.4
  • 189
    • 0000219702 scopus 로고
    • Reviews on asymmetric protonation using chiral proton sources: a) L. Duhamel. P. Duhamel, J.-C. Launay, J.-C. Plaquevent, Bull. Soc. Chim. Fr. 1984, 421-430; b) S. Hunig in Methods Org. Chem. (Houben-Weyl) 4th ed. 1952-, Vol. E21, 1995, pp. 3851-3911: c) C. Fehr, Angew. Chem. 1996, 108, 2726-2748; Angew. Chem. Int. Ed. Engl. 1996, 35, 2566-2587.
    • (1995) Methods Org. Chem. (Houben-Weyl) 4th ed. 1952-, Vol. E21 , vol.E21 , pp. 3851-3911
    • Hunig, S.1
  • 190
    • 0000530876 scopus 로고    scopus 로고
    • Reviews on asymmetric protonation using chiral proton sources: a) L. Duhamel. P. Duhamel, J.-C. Launay, J.-C. Plaquevent, Bull. Soc. Chim. Fr. 1984, 421-430; b) S. Hunig in Methods Org. Chem. (Houben-Weyl) 4th ed. 1952-, Vol. E21, 1995, pp. 3851-3911: c) C. Fehr, Angew. Chem. 1996, 108, 2726-2748; Angew. Chem. Int. Ed. Engl. 1996, 35, 2566-2587.
    • (1996) Angew. Chem. , vol.108 , pp. 2726-2748
    • Fehr, C.1
  • 191
    • 33751146774 scopus 로고    scopus 로고
    • Reviews on asymmetric protonation using chiral proton sources: a) L. Duhamel. P. Duhamel, J.-C. Launay, J.-C. Plaquevent, Bull. Soc. Chim. Fr. 1984, 421-430; b) S. Hunig in Methods Org. Chem. (Houben-Weyl) 4th ed. 1952-, Vol. E21, 1995, pp. 3851-3911: c) C. Fehr, Angew. Chem. 1996, 108, 2726-2748; Angew. Chem. Int. Ed. Engl. 1996, 35, 2566-2587.
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 2566-2587
  • 195
    • 33845557266 scopus 로고
    • The regioselectivities of the [2,3] and [1,2] Wittig rearrangement of bisallylic and allyl propargyl ethers: a) T. Nakai, K. Mikami, S. Taya, Y. Fujita, J. Am. Chem. Soc. 1981, 103, 6492-6494; b) K. Mikami, N. Kishi, T. Nakai, Chem. Lett. 1982, 1643-1646; c) K. Mikami, K. Azuma, T. Nakai, Tetrahedron 1984, 40, 2303-2308; d) K. Mikami, N. Kishi, T. Nakai, Chem. Lett. 1989, 1683-1686.
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 6492-6494
    • Nakai, T.1    Mikami, K.2    Taya, S.3    Fujita, Y.4
  • 196
    • 33845557266 scopus 로고
    • The regioselectivities of the [2,3] and [1,2] Wittig rearrangement of bisallylic and allyl propargyl ethers: a) T. Nakai, K. Mikami, S. Taya, Y. Fujita, J. Am. Chem. Soc. 1981, 103, 6492-6494; b) K. Mikami, N. Kishi, T. Nakai, Chem. Lett. 1982, 1643-1646; c) K. Mikami, K. Azuma, T. Nakai, Tetrahedron 1984, 40, 2303-2308; d) K. Mikami, N. Kishi, T. Nakai, Chem. Lett. 1989, 1683-1686.
    • (1982) Chem. Lett. , pp. 1643-1646
    • Mikami, K.1    Kishi, N.2    Nakai, T.3
  • 197
    • 0000007105 scopus 로고
    • The regioselectivities of the [2,3] and [1,2] Wittig rearrangement of bisallylic and allyl propargyl ethers: a) T. Nakai, K. Mikami, S. Taya, Y. Fujita, J. Am. Chem. Soc. 1981, 103, 6492-6494; b) K. Mikami, N. Kishi, T. Nakai, Chem. Lett. 1982, 1643-1646; c) K. Mikami, K. Azuma, T. Nakai, Tetrahedron 1984, 40, 2303-2308; d) K. Mikami, N. Kishi, T. Nakai, Chem. Lett. 1989, 1683-1686.
    • (1984) Tetrahedron , vol.40 , pp. 2303-2308
    • Mikami, K.1    Azuma, K.2    Nakai, T.3
  • 198
    • 33845557266 scopus 로고
    • The regioselectivities of the [2,3] and [1,2] Wittig rearrangement of bisallylic and allyl propargyl ethers: a) T. Nakai, K. Mikami, S. Taya, Y. Fujita, J. Am. Chem. Soc. 1981, 103, 6492-6494; b) K. Mikami, N. Kishi, T. Nakai, Chem. Lett. 1982, 1643-1646; c) K. Mikami, K. Azuma, T. Nakai, Tetrahedron 1984, 40, 2303-2308; d) K. Mikami, N. Kishi, T. Nakai, Chem. Lett. 1989, 1683-1686.
    • (1989) Chem. Lett. , pp. 1683-1686
    • Mikami, K.1    Kishi, N.2    Nakai, T.3
  • 208
    • 0001106853 scopus 로고    scopus 로고
    • Polymer-supported, achiral Sc catalyst: a) S. Nagayama, S. Kobayashi, Angew. Chem. 2000, 112, 578-581; Angew. Chem. Int. Ed. 2000, 39, 567-569; b) M. T. Reetz, D. Giebel. Angew. Chem. 2000, 112 12, 2614-2617; Angew. Chem. Int. Ed. 2000, 39, 2498-2501.
    • (2000) Angew. Chem. , vol.112 , pp. 578-581
    • Nagayama, S.1    Kobayashi, S.2
  • 209
    • 0034602986 scopus 로고    scopus 로고
    • Polymer-supported, achiral Sc catalyst: a) S. Nagayama, S. Kobayashi, Angew. Chem. 2000, 112, 578-581; Angew. Chem. Int. Ed. 2000, 39, 567-569; b) M. T. Reetz, D. Giebel. Angew. Chem. 2000, 112 12, 2614-2617; Angew. Chem. Int. Ed. 2000, 39, 2498-2501.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 567-569
  • 210
    • 0000932427 scopus 로고    scopus 로고
    • Polymer-supported, achiral Sc catalyst: a) S. Nagayama, S. Kobayashi, Angew. Chem. 2000, 112, 578-581; Angew. Chem. Int. Ed. 2000, 39, 567-569; b) M. T. Reetz, D. Giebel. Angew. Chem. 2000, 112 12, 2614-2617; Angew. Chem. Int. Ed. 2000, 39, 2498-2501.
    • (2000) Angew. Chem. , vol.112 , pp. 2614-2617
    • Reetz, M.T.1    Giebel, D.2
  • 211
    • 0034679481 scopus 로고    scopus 로고
    • Polymer-supported, achiral Sc catalyst: a) S. Nagayama, S. Kobayashi, Angew. Chem. 2000, 112, 578-581; Angew. Chem. Int. Ed. 2000, 39, 567-569; b) M. T. Reetz, D. Giebel. Angew. Chem. 2000, 112 12, 2614-2617; Angew. Chem. Int. Ed. 2000, 39, 2498-2501.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 2498-2501


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.