Asymmetric total synthesis of (+)-didemniserinolipid b via achmatowicz rearrangement/bicycloketalization

Journal of Organic Chemistry

Volumn 79, Issue 15, 2014, Pages 6987-6995

  Ren, Jingyun ^a   Tong, Rongbiao ^a  

^a HONG KONG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Hong Kong)

Author keywords

[No Author keywords available]

Indexed keywords

BIOACTIVITY;

ASYMMETRIC TOTAL SYNTHESIS; CONVERGENT SYNTHETIC STRATEGY; ENANTIOSELECTIVE CONSTRUCTION; SYNTHETIC STRATEGIES; TOTAL SYNTHESIS;

SYNTHESIS (CHEMICAL);

6,8 DIOXABICYCLO[3.2.1]OCTANE; CYCLOOCTANE DERIVATIVE; DIDEMNISERINOLIPID A; DIDEMNISERINOLIPID B; DIDEMNISERINOLIPID C; LIPID; UNCLASSIFIED DRUG; 6,8-DIOXABICYCLO(3.2.1)OCTANE; BICYCLO COMPOUND; FUSED HETEROCYCLIC RINGS; PROPANEDIOL DERIVATIVE;

ACHMATOWICZ REARRANGEMENT; ARTICLE; BIOLOGICAL ACTIVITY; CHEMICAL REACTION; RING CLOSING METATHESIS; SYNTHESIS; BIOCHEMISTRY; CHEMICAL STRUCTURE; CHEMISTRY; CYCLIZATION; STEREOISOMERISM;

BICYCLO COMPOUNDS; BICYCLO COMPOUNDS, HETEROCYCLIC; BIOCHEMICAL PROCESSES; CYCLIZATION; MOLECULAR STRUCTURE; PROPYLENE GLYCOLS; STEREOISOMERISM;

EID: 84905370580     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo501142q     Document Type: Article

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