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Volumn 46, Issue 46, 2005, Pages 7931-7934

An efficient asymmetric synthesis of grenadamide

Author keywords

Elimination; Cyclopropanation; Natural product; syn aldol; Temporary stereocentre

Indexed keywords

5,5 DIMETHYLOXAZOLIDIN 2 ONE; CYCLOPROPANE DERIVATIVE; GRENADAMIDE; HYDROXYL GROUP; NATURAL PRODUCT; OXAZOLIDINONE DERIVATIVE; PHENETHYLAMINE; UNCLASSIFIED DRUG;

EID: 26844501274     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.09.087     Document Type: Article
Times cited : (26)

References (22)
  • 8
    • 26844433390 scopus 로고    scopus 로고
    • Ref. 3.
    • These conditions have been used previously for the preparation of syn-aldols derived from N-acyl-oxazolidin-2-ones, see: (a) Ref. 3.
  • 13
    • 0037467051 scopus 로고    scopus 로고
    • For a discussion on the mechanism of directed cyclopropanation reactions of allylic alcohols, see: M. Nakamura, A. Hirai, and E. Nakamura J. Am. Chem. Soc. 125 2003 2341 2350
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 2341-2350
    • Nakamura, M.1    Hirai, A.2    Nakamura, E.3
  • 14
    • 26844475238 scopus 로고    scopus 로고
    • note
    • 4 requires 467.2671).
  • 15
    • 26844548195 scopus 로고    scopus 로고
    • note
    • 2 requires 366.2194).
  • 16
    • 0002078745 scopus 로고    scopus 로고
    • Similar cleavage conditions have been reported for the direct aminolysis of N-acyl-pyrrolidones, containing gem-dimethyl groups, see: S.G. Davies, and D.J. Dixon Synlett 1998 963 964
    • (1998) Synlett , pp. 963-964
    • Davies, S.G.1    Dixon, D.J.2
  • 20
    • 26844544620 scopus 로고    scopus 로고
    • note
    • 32NO requires 314.2477).
  • 22
    • 26844494689 scopus 로고    scopus 로고
    • note
    • 34NO requires 316.2635).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.