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Volumn 44, Issue 10, 2005, Pages 1549-1551

Powerful chiral phase-transfer catalysts for the asymmetric synthesis of α-alkyl- and α,α-dialkyl-α-amino acids

Author keywords

Alkylation; Amino acids; Enantioselectivity; Glycine; Phase transfer catalysis

Indexed keywords

ALKYLATION; CATALYST ACTIVITY; DERIVATIVES; PHASE TRANSITIONS; RATE CONSTANTS; SYNTHESIS (CHEMICAL);

EID: 16244410177     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200462257     Document Type: Article
Times cited : (209)

References (34)
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    • (Eds.: Y. Sasson, R. Neumann), Blackie, London
    • c) Handbook of Phase-Transfer Catalysis (Eds.: Y. Sasson, R. Neumann), Blackie, London, 1997;
    • (1997) Handbook of Phase-Transfer Catalysis
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    • American Chemical Society, Washington (ACS Symposium Series 659)
    • d) Phase-Transfer Catalysis (Ed.: M. E. Halpern), American Chemical Society, Washington, 1997 (ACS Symposium Series 659).
    • (1997) Phase-Transfer Catalysis
    • Halpern, M.E.1
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    • (Eds.: Y. Sasson, R. Neumann), Blackie, London, chap 14
    • Reviews: a) T. Shioiri in Handbook of Phase-Transfer Catalysis (Eds.: Y. Sasson, R. Neumann), Blackie, London, 1997, chap. 14;
    • (1997) Handbook of Phase-Transfer Catalysis
    • Shioiri, T.1
  • 8
    • 0002855131 scopus 로고    scopus 로고
    • (Eds.: F. Vögtle, J. F. Stoddart, M. Shibasaki), Wiley-VCH, Weinheim
    • d) T. Shioiri, S. Arai in Stimulating Concepts in Chemistry (Eds.: F. Vögtle, J. F. Stoddart, M. Shibasaki), Wiley-VCH, Weinheim, 2000, p. 123.
    • (2000) Stimulating Concepts in Chemistry , pp. 123
    • Shioiri, T.1    Arai, S.2
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    • i) H.-g. Park, B.-S. Jeong, M.-S. Yoo, J.-H. Lee, M.-k. Park, Y.-J. Lee, M.-J. Kim, S.-s. Jew, Angew. Chem. 2002, 114, 3162; Angew. Chem. Int. Ed. 2002, 41, 3036;
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 3036
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    • j) T. Kita, A. Georgieva, U. Hashimoto, T. Nakata, K. Nagasawa, Angew. Chem. 2002, 114, 2956; Angew. Chem. Int. Ed. 2002, 41, 2832
    • (2002) Angew. Chem. Int. Ed. , vol.41 , pp. 2832
  • 33
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    • - salt] contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
  • 34
    • 16244411916 scopus 로고    scopus 로고
    • note
    • 2Ph) in only 22% yield with 85% ee.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.