Combined C-H activation/cope rearrangement as a strategic reaction in organic synthesis: Total synthesis of (-)-colombiasin A and (-)-elisapterosin B

Journal of the American Chemical Society

Volumn 128, Issue 7, 2006, Pages 2485-2490

  Davies, Huw M L ^a   Dai, Xing ^a   Long, Matthew S ^a  

^a UNIVERSITY AT BUFFALO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARBON; HYDROGEN; REACTION KINETICS; SYNTHESIS (CHEMICAL);

CYCLOPROPANATION; ENANTIOMERS; NATURAL PRODUCTS;

CHEMICAL ACTIVATION;

1 METHYL 1,2 DIHYDRONAPHTHALENE; AZO COMPOUND; BENZENESULFONIC ACID DERIVATIVE; CARBON; COLOMBIASIN A; DIRHODIUM TETRAKIS(N DODECYLBENZENESULFONYL)PROLINATE; ELISAPTEROSIN B; HYDROGEN; METHYL 2 DIAZO 3 PENTENOATE; NAPHTHALENE DERIVATIVE; NATURAL PRODUCT; PENTANE; PROLINE DERIVATIVE; RHODIUM COMPLEX; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CHEMICAL REACTION; CONFORMATION; COPE REARRANGEMENT; CYCLOPROPANATION; ENANTIOMER; STEREOCHEMISTRY; SYNTHESIS;

BRIDGED COMPOUNDS; DITERPENES; STEREOISOMERISM;

EID: 33644544051     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja056877l     Document Type: Article

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