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Volumn 119, Issue 26, 1997, Pages 6040-6047

Asymmetric C-N bond constructions via crotylsilane addition reactions: A stereocontrolled route to dipeptide isosteres

Author keywords

[No Author keywords available]

Indexed keywords

PEPTIDE DERIVATIVE; SILANE DERIVATIVE;

EID: 0030834303     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja964364w     Document Type: Article
Times cited : (40)

References (52)
  • 24
    • 16944363905 scopus 로고    scopus 로고
    • note
    • 4/S, all of which resulted in complex mixtures.
  • 25
    • 16944364907 scopus 로고    scopus 로고
    • note
    • 13C NMR, IR, MS, and HRMS spectral data.
  • 27
    • 16944363664 scopus 로고    scopus 로고
    • note
    • 4 is commercially available from Aldrich Chemical Co.
  • 28
    • 16944363720 scopus 로고    scopus 로고
    • note
    • 1H NMR of these substrates indicated substantial desilation and displayed a para-substituted splitting pattern of the aromatic protons.
  • 29
    • 84943392701 scopus 로고
    • Aziridines, azines and fused ring derivatives
    • Lwowski, W., Ed.; Pergamon Press: Oxford
    • (a) Padwa, A; Woolhouse, A. D. Aziridines, Azines and fused ring derivatives. In Comprehensive Hetereocyclic Chemistry; Lwowski, W., Ed.; Pergamon Press: Oxford, 1984; Vol. 7.
    • (1984) Comprehensive Hetereocyclic Chemistry , vol.7
    • Padwa, A.1    Woolhouse, A.D.2
  • 30
    • 0003540629 scopus 로고
    • Hassner, A., Ed.; John Wiley and Sons: New York, Part 1. Ring opening of aziridines
    • (b) Deyrup, J. A. In The Chemistry of Heterocyclic Compounds; Hassner, A., Ed.; John Wiley and Sons: New York, 1983; Vol. 42, Part 1. Ring opening of aziridines:
    • (1983) The Chemistry of Heterocyclic Compounds , vol.42
    • Deyrup, J.A.1
  • 41
    • 0000403720 scopus 로고
    • The PhI=NTs was prepared according to Yamada et al. (Yamada, Y.; Yamamoto, T.; Okawara, M. Chem Lett. 1975, 361-362) with modifications as described in the Experimental Section.
    • (1975) Chem Lett. , pp. 361-362
    • Yamada, Y.1    Yamamoto, T.2    Okawara, M.3
  • 43
    • 16944365636 scopus 로고    scopus 로고
    • Commercially available from Aldrich Chemical Co.
    • Commercially available from Aldrich Chemical Co.
  • 45
    • 16944366675 scopus 로고    scopus 로고
    • note
    • Proof of the absolute stereochemistry of the allylic N-tosylamines was obtained by correlation of the known allylic nitro compound 2a to the allylic N-tosylamine 7a via the following sequence: (see Supporting Information for experimental details).
  • 50
    • 16944362716 scopus 로고    scopus 로고
    • See the Experimental Section for the preparation of silanes 6f and 6g
    • See the Experimental Section for the preparation of silanes 6f and 6g.
  • 51
    • 0000458209 scopus 로고
    • For an excellent and comprehensive review of substrate-directable reactions, see: Hoveyda, A. H.; Evans, D. A.; Fu, G. C. Chem. Rev. 1993, 93, 1307-1370.
    • (1993) Chem. Rev. , vol.93 , pp. 1307-1370
    • Hoveyda, A.H.1    Evans, D.A.2    Fu, G.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.