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Volumn 7, Issue 20, 2009, Pages 4285-4288

Accessible sugars as asymmetric olefin epoxidation organocatalysts: Glucosaminide ketones in the synthesis of terminal epoxides

Author keywords

[No Author keywords available]

Indexed keywords

ASYMMETRIC EPOXIDATION; N-ACETYL-D-GLUCOSAMINE; OLEFIN EPOXIDATION; ORGANOCATALYSTS; TERMINAL EPOXIDE; TERMINAL OLEFINS;

EID: 70349835637     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b911675c     Document Type: Article
Times cited : (25)

References (27)
  • 7
    • 0037288744 scopus 로고    scopus 로고
    • For general reviews, see:
    • T. Katsuki Synlett 2003 281
    • (2003) Synlett , pp. 281
    • Katsuki, T.1
  • 19
    • 0035313421 scopus 로고    scopus 로고
    • The procedure reported by Shibasaki requires the preparation of a complex chiral multimetallic complex and its applicability is limited by the presence of basic-labile groups and/or epimerisable positions, whereas the current disadvantage with regard to catalysts 1-4 is the lengthy synthetic sequence reported for their synthesis giving low overall preparative yields
    • A. Archelas R. Furtoss Curr. Opin. Chem. Biol. 2001 5 112
    • (2001) Curr. Opin. Chem. Biol. , vol.5 , pp. 112
    • Archelas, A.1    Furtoss, R.2
  • 23
    • 0034608915 scopus 로고    scopus 로고
    • ® and olefin occurs at a negligible rate It should be noted that good conversions (up to 91%) for 2-vinylnaphthalene 12 could be reached although with complete loss of stereoselectivity by using ketone 8 (see ESI for full details)
    • A. Armstrong I. Washington K. N. Houk J. Am. Chem. Soc. 2000 122 6297
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 6297
    • Armstrong, A.1    Washington, I.2    Houk, K.N.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.