Stereoselective syntheses of four diastereomers of 3,9,12- trihydroxycalamenene via a benzobicyclo[3.3.1] intermediate

Journal of Organic Chemistry

Volumn 75, Issue 12, 2010, Pages 4224-4229

  Sun, Yongquan ^a   Yu, Binxun ^a   Wang, Xiaolei ^a   Tang, Shibing ^a   She, Xuegong ^a   Pan, Xinfu ^a  

^a LANZHOU UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

DIASTEREOMERS; FRIEDEL-CRAFTS; MICHAEL ADDITIONS; STEREOSELECTIVE SYNTHESIS;

ADDITION REACTIONS;

STEREOSELECTIVITY;

3,9,12 TRIHYDROXYCALAMENENE; ALPHA,BETA LACTONE DERIVATIVE; AMPHILECTANE; BENZOBIACYCLO[3.3.1]LACTONE DERIVATIVE; LACTONE DERIVATIVE; SERRULATANE; UNCLASSIFIED DRUG;

ALLYLATION; ARTICLE; CHEMICAL STRUCTURE; DIASTEREOISOMER; FRIEDEL CRAFTS REACTION; STEREOCHEMISTRY; SYNTHESIS;

BICYCLO COMPOUNDS; LACTONES; MOLECULAR STRUCTURE; STEREOISOMERISM; TERPENES;

EID: 77953529895     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo1008349     Document Type: Article

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