메뉴 건너뛰기




Volumn 1, Issue 24, 2003, Pages 4364-4366

Synthesis of the cyclobutane core of solanoeclepin A via intramolecular allene butenolide photocycloaddition

Author keywords

[No Author keywords available]

Indexed keywords

BIOCHEMISTRY; CHEMICAL BONDS; CRYSTALLINE MATERIALS; HYDROXYLATION; OXIDATION; PH EFFECTS; PHOTOCHEMICAL REACTIONS; STEREOCHEMISTRY; STRUCTURE (COMPOSITION); SYNTHESIS (CHEMICAL); X RAY ANALYSIS;

EID: 0347537949     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b311415e     Document Type: Article
Times cited : (33)

References (28)
  • 7
    • 33845376909 scopus 로고
    • The most direct approach to the bicyclo[2.1.1]hexanone would be an intramolecular ketene olefin cycloaddition, but this process was expected to be unproductive on the basis of literature precedent: B. B. Snider and R. A. H. F. Hui, J. Org. Chem., 1985, 50, 5167-5176.
    • (1985) J. Org. Chem. , vol.50 , pp. 5167-5176
    • Snider, B.B.1    Hui, R.A.H.F.2
  • 21
    • 0030730768 scopus 로고    scopus 로고
    • (b) For intramolecular β-lactone photocycloadditions of enantiopure allenes, see M. S. Shepard and E. M. Carreira, Tetrahedron, 1997, 53, 16253-16276.
    • (1997) Tetrahedron , vol.53 , pp. 16253-16276
    • Shepard, M.S.1    Carreira, E.M.2
  • 24
    • 0346340353 scopus 로고    scopus 로고
    • The reported instability of the natural product in basic medium may be associated with the β-hydroxyketone moiety
    • The reported instability of the natural product in basic medium may be associated with the β-hydroxyketone moiety.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.