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Volumn 47, Issue 3, 1991, Pages 481-496

Radical cyclization strategies to terpenoids; syntheses of (±)-β-cuparenone, (±)-laurene and epilaurenes

Author keywords

[No Author keywords available]

Indexed keywords

BETA CUPARENONE; CUPARENE; LAURENE; TERPENOID; UNCLASSIFIED DRUG;

EID: 0026074793     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)90504-6     Document Type: Article
Times cited : (25)

References (48)
  • 6
    • 85082777144 scopus 로고
    • The Design and Application of Free Radical Chain Reactions in Organic Synthesis. Part 1
    • (1988) Synthesis , pp. 417
    • Curran1
  • 7
    • 85064667006 scopus 로고
    • The Design and Application of Free Radical Chain Reactions in Organic Synthesis. Part 2
    • (1988) Synthesis , pp. 489
    • Curran1
  • 45
    • 84918234287 scopus 로고    scopus 로고
    • As the intermediate radical equilibrates much faster than it cyclizes, the stereochemistry of the starting alcohol has no significance and provides the same (1:1) stereomixture of cyclized products.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.