A convergent and stereocontrolled cycloaddition strategy toward eudesmane sesquiterpenoid: Total synthesis of (±)-6β,14-epoxyeudesm-4(15)-en- 1β-ol

Journal of Organic Chemistry

Volumn 77, Issue 9, 2012, Pages 4217-4225

  Wang, Cui Cui ^a   Li, Wei Dong Z ^a,b  

^a LANZHOU UNIVERSITY   (China)

^b NANKAI UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

BUILDING BLOCKES; DIELS-ALDER; FUNCTIONALIZED; SESQUITERPENOIDS; TOTAL SYNTHESIS;

MALEIC ANHYDRIDE;

CYCLOADDITION;

6BETA,14 EPOXYEUDESM 4(15) EN 1 BETA OL; BENZOIC ACID DERIVATIVE; CARBON; CARBOXYLIC ACID DERIVATIVE; MALEIC ANHYDRIDE; SESQUITERPENE; UNCLASSIFIED DRUG;

ARTICLE; CYCLOADDITION; DIELS ALDER REACTION; OXYGENATION; STEREOCHEMISTRY; SYNTHESIS;

CYCLIZATION; MOLECULAR STRUCTURE; SESQUITERPENES, EUDESMANE; STEREOISOMERISM;

EID: 84860621671     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo300556r     Document Type: Article

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