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Volumn 56, Issue 3, 2000, Pages 425-439

Enantioselective synthetic methodology to prepare trans-fused bicyclo[5.3.0]decane Systems: An approach to the synthesis of the pseudoguaiane carbon framework

Author keywords

Bicyclo 5.3.0 decane; Enantioselective synthesis; Nicholas reaction; Pseudoguaiane; 4+3 cycloaddition

Indexed keywords

BICYCLO[5.3.0]DECANE DERIVATIVE; DECANE; NATURAL PRODUCT; PSEUDOGUAIANE; SESQUITERPENE; UNCLASSIFIED DRUG;

EID: 0342948830     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(99)01009-1     Document Type: Article
Times cited : (40)

References (104)
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    • For enantioselective deprotonation of cyclic ketones see: (a) Majewski, M.; Lazny, R. J. Org.Chem. 1995, 60, 5825.
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    • Ref. 11d.
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    • note
    • Supplier: Fluka. (+)-Bis-[(7?)-1-phenylethylamine] hydrochloride, Ref. 15147. (-)-Enantiomer, Ref. 15145.
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    • Supplementary material available. Complete crystal data, list of refined coordinates and a complete list of bond distances are available on request from the Director of the Cambridge Crystallographic Data Centre, University Chemical Laboratory, Lensfield Road, Cambridge CB2 1EW. Any request should be accompanied by the full literature citation for this work. See Tetrahedron 1984, 40, 2, ii.
    • (1984) Tetrahedron , vol.40 , pp. 2
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    • Technische Universität Berlin: Germany
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.