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Volumn 31, Issue 1, 1998, Pages 3-15

Applications of cis-1-Amino-2-indanol in asymmetric synthesis

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EID: 0032409293     PISSN: 00025100     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (90)

References (104)
  • 1
    • 0003400107 scopus 로고
    • John Wiley and Sons: New York
    • A great deal of synthetic effort has been devoted to the binaphthyl platform (BINOL, BINAP, etc.) as a chiral template, which has become the benchmark for asymmetric synthesis. Noyori R. Asymmetric Catalysis in Organic Synthesis: John Wiley and Sons: New York, 1994.
    • (1994) Asymmetric Catalysis in Organic Synthesis
    • Noyori, R.1
  • 12
    • 0000454231 scopus 로고    scopus 로고
    • and references therein
    • For an industrial asymmetric synthesis of a single enantiomer of Crixivan®, see: Reider, P.J. Chimia 1997, 51, 306 and references therein.
    • (1997) Chimia , vol.51 , pp. 306
    • Reider, P.J.1
  • 33
    • 0002578608 scopus 로고
    • Asymmetric catalytic epoxidation of unfunctionalized olefins
    • Ojima, I., Ed.; VCH: New York, Chapter 4.2, and references therein
    • (a) Preparation of chiral styrene oxide derivatives via asymmetric metal catalysis: Jacobsen, E. N. Asymmetric Catalytic Epoxidation of Unfunctionalized Olefins. In Catalytic Asymmetric Synthesis; Ojima, I., Ed.; VCH: New York, 1993, Chapter 4.2, p159 and references therein.
    • (1993) Catalytic Asymmetric Synthesis , pp. 159
    • Jacobsen, E.N.1
  • 44
    • 0013476098 scopus 로고    scopus 로고
    • unpublished results
    • (l) Indene has been converted to cis-indenediol in >99% ee with dioxygenase: Greasham, R. et al. unpublished results.
    • Greasham, R.1
  • 48
    • 0013476250 scopus 로고    scopus 로고
    • Available from Aldrich Chemical Co., Inc.
    • (a) Available from Aldrich Chemical Co., Inc.
  • 49
    • 0013513473 scopus 로고    scopus 로고
    • Multikilogram quantities are available from ChiRex, Newcastle, England
    • (b) Multikilogram quantities are available from ChiRex, Newcastle, England.
  • 54
    • 0000818237 scopus 로고
    • (b) For a review of the Ritter reaction, see Bishop, R. Comp. Org. Synth. 1991, 6, 261.
    • (1991) Comp. Org. Synth. , vol.6 , pp. 261
    • Bishop, R.1
  • 73
    • 0001821044 scopus 로고
    • Practical asymmetric synthesis of (-)-menthol and related terpenoids
    • Noyori, R.; Hiraoka, T.; Mori, K.; Murahashi, S.; Onada, T.; Suzuki, K.; Yonemitsu, O., Eds.; Tokyo Kagaku Dozin: Tokyo
    • (a) Noyori's BINAP-Rh complex-catalyzed enantioselective isomerization of diethylgeranylamine in the production of (-)-menthol: Akutagawa, S. Practical Asymmetric Synthesis of (-)-Menthol and Related Terpenoids. In Organic Synthesis in Japan: Past, Present, and Future; Noyori, R.; Hiraoka, T.; Mori, K.; Murahashi, S.; Onada, T.; Suzuki, K.; Yonemitsu, O., Eds.; Tokyo Kagaku Dozin: Tokyo, 1992; p 75.
    • (1992) Organic Synthesis in Japan: Past, Present, and Future , pp. 75
    • Akutagawa, S.1
  • 74
    • 0013479190 scopus 로고    scopus 로고
    • Jacobsen's Mn-(salen) catalyst for epoxidation of indene in the synthesis of HIV protease inhibitor Crixivan®: references 6 and 9c
    • (b) Jacobsen's Mn-(salen) catalyst for epoxidation of indene in the synthesis of HIV protease inhibitor Crixivan®: references 6 and 9c.
  • 76
    • 0025910637 scopus 로고
    • Stoichiometric amounts of amino alcohols: Catalytic reductions
    • (a) Stoichiometric amounts of amino alcohols: Didier, E.; Loubinoux, B.; Ramos Tombo, G.M.; Rihs, G. Tetrahedron 1991, 47, 4941. Catalytic reductions:
    • (1991) Tetrahedron , vol.47 , pp. 4941
    • Didier, E.1    Loubinoux, B.2    Ramos Tombo, G.M.3    Rihs, G.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.