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Volumn 20, Issue 15, 2009, Pages 1802-1805

Stereoselective synthesis of 2-epi-jaspine B via base-catalyzed intramolecular oxy-Michael conjugate addition approach

Author keywords

[No Author keywords available]

Indexed keywords

2 EPI JASPINE B; PHYTOSPHINGOSINE; TARTARIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

EID: 69149096020     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2009.07.004     Document Type: Article
Times cited : (33)

References (35)
  • 14
    • 43649103123 scopus 로고    scopus 로고
    • For synthetic strategies and structural assignment of jaspine B and 2-epi-jaspine B, see:
    • For synthetic strategies and structural assignment of jaspine B and 2-epi-jaspine B, see:. Abraham E., Davies S.G., Roberts P.M., Russell A.J., and Thomson E. Tetrahedron: Asymmetry 19 (2008) 1027-1047
    • (2008) Tetrahedron: Asymmetry , vol.19 , pp. 1027-1047
    • Abraham, E.1    Davies, S.G.2    Roberts, P.M.3    Russell, A.J.4    Thomson, E.5
  • 32
    • 69149105673 scopus 로고    scopus 로고
    • note
    • 13C NMR spectrum thus indicating the formation of a five-membered acetonide.
  • 33
    • 0033597805 scopus 로고    scopus 로고
    • For recent examples of the oxy-Michael reaction, see:
    • For recent examples of the oxy-Michael reaction, see:. Honda T., and Ishikawa F. J. Org. Chem. 64 (1999) 5542-5546
    • (1999) J. Org. Chem. , vol.64 , pp. 5542-5546
    • Honda, T.1    Ishikawa, F.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.