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Volumn , Issue 12, 2001, Pages 2371-2377

Synthesis of the right-hand substructure of solanoeclepin A

Author keywords

Cyclization; Cycloaddition; Natural products; Photochemistry

Indexed keywords

BICYCLO COMPOUND; CYCLOBUTANONE DERIVATIVE; CYCLOPROPANE; HEXANE; SOLANOECLEPIN A; UNCLASSIFIED DRUG;

EID: 0034977491     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200106)2001:12<2371::AID-EJOC2371>3.0.CO;2-O     Document Type: Article
Times cited : (41)

References (25)
  • 10
    • 0004769903 scopus 로고    scopus 로고
    • note
    • The reaction performed with lithium bases led to a complex mixture of products. We assume that the dioxenone moiety undergoes an attack of the generated oxoanion leading to ring opening side-reactions.
  • 16
    • 0004752211 scopus 로고    scopus 로고
    • note
    • Crystallographic data (excluding structure factors) for the structure reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-155465. Copies of the data can be obtained free of charge on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK [Fax: (internat.) +44-1223/336-033; E-mail: deposit@ccdc.cam.ac.uk].
  • 19
    • 0000134379 scopus 로고
    • (Eds.: E. W. Abel, F. G. A. Stone, G. Wilkinson), Pergamon: Oxford
    • [16a] M. P. Doyle, in Comprehensive Organometallic Chemistry II (Eds.: E. W. Abel, F. G. A. Stone, G. Wilkinson), Pergamon: Oxford, 1995, Vol. 12, pp 387-420.
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 387-420
    • Doyle, M.P.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.