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Volumn 64, Issue 8, 1999, Pages 2914-2918

Enantioselective synthesis of α-amino acids from chiral 1,4- benzodiazepine-2,5-diones containing the α-phenethyl group

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA AMINO ACID; BENZODIAZEPIN 2 ONE DERIVATIVE; GLYCINE DERIVATIVE;

EID: 0039255361     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo980777z     Document Type: Article
Times cited : (32)

References (52)
  • 1
    • 84945031690 scopus 로고
    • Springer-Verlag, has been dedicated to the subject since
    • In addition to a substantial number of monographs, a periodical journal, Amino Acids, Springer-Verlag, has been dedicated to the subject since 1994.
    • (1994) Amino Acids
  • 2
    • 0001039009 scopus 로고
    • α-Amino acid synthesis
    • Tetrahedron Symposium-in-Print
    • (a) O'Donnell, M. J., Ed. α-Amino Acid Synthesis (Tetrahedron Symposium-in-Print) Tetrahedron 1988, 44, 5253-5614.
    • (1988) Tetrahedron , vol.44 , pp. 5253-5614
    • O'Donnell, M.J.1
  • 7
    • 0028130028 scopus 로고
    • (c) Cole, D. C. Tetrahedron 1994, 50, 9517-9582.
    • (1994) Tetrahedron , vol.50 , pp. 9517-9582
    • Cole, D.C.1
  • 9
    • 0001622386 scopus 로고
    • See, for example: (a) Schoellkopf, U. Tetrahedron 1983, 39, 2085-2091.
    • (1983) Tetrahedron , vol.39 , pp. 2085-2091
    • Schoellkopf, U.1
  • 18
    • 0345482720 scopus 로고    scopus 로고
    • note
    • Atomic coordinates for all the structures reported in this paper have been deposited with the Cambridge Crystallographic Data Centre. The coordinates can be obtained, on request, from the Director, Cambridge Crystallographic Centre, 12 Union Road, Cambridge CB2 IEZ, U.K.
  • 23
  • 35
    • 0000254037 scopus 로고
    • The idea behind the use of 6 equiv of the cosolvent is that this will lead to tetrasolvated lithium cation and an essentially free anion instead of a contact ion pair or aggregate thereof: (a) Reich, H. J.; Borst, J. P. J. Am. Chem. Soc. 1991, 113, 1835-1837.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 1835-1837
    • Reich, H.J.1    Borst, J.P.2
  • 39
    • 0344188837 scopus 로고    scopus 로고
    • note
    • The major isomer was separated prior to hydrolysis, so that enantiopure amino acids may be obtained.
  • 46
    • 0030878921 scopus 로고    scopus 로고
    • (b) For a detailed description of the computational method, see: Cuevas, G.; Juaristi, E. J. Am. Chem. Soc. 1997, 119, 7545.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 7545
    • Cuevas, G.1    Juaristi, E.2
  • 47
    • 0040723847 scopus 로고
    • Aldrich: Milwaukee
    • Aldrich Chemical Catalogue, 1994-1995; Aldrich: Milwaukee, 1994; (a) p 37; (b) p 61; (c) p 1064; (d) p 1115; (e) p 1102.
    • (1994) Aldrich Chemical Catalogue, 1994-1995


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.