A stereoselective aldol approach for the total synthesis of herbarumin I and stagonolide A

Synthesis

Volumn , Issue 14, 2010, Pages 2407-2412

  Srihari, P ^a   Rao, G Maheswara ^a   Rao, R Srinivasa ^a   Yadav, J S ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

Evans aldol; macrolide; olefin metathesis; phytotoxic

Indexed keywords

MACROLIDES; OLEFIN METATHESIS; PHYTOTOXIC COMPOUNDS; RING-CLOSING OLEFIN METATHESIS; STEREO-SELECTIVE; TOTAL SYNTHESIS;

OLEFINS; STEREOSELECTIVITY;

SYNTHESIS (CHEMICAL);

2 (BENZYLOXY) 1 (4 BENZYL 2 THIOXOOXAZOLIDIN 3 YL) 3 (TERT BUTYLDIMETHYLSILYLOXY)HEXAN 1 ONE; 2 (BENZYLOXY) 1 (4 BENZYL 2 THIOXOOXAZOLIDIN 3 YL) 3 HYDROXYHEXAN 1 ONE; 2 (BENZYLOXY) 1 (4 BENZYL 2 THIOXOOXAZOLIDIN 3 YL)ETHANONE; 2 (BENZYLOXY) 3 (TERT BUTYLDIMETHYLSILYLOXY)HEXANAL; 4 (BENZYLOXY) 5 (TERT BUTYLDIMETHYLSILYLOXY)OCT 1 EN 3 OL; 5,6 BIS(BENZYLOXY)OCT 7 EN 4 OL; 5,6 BIS(BENZYLOXY)OCT 7 EN 4 YL HEX 5 ENOATE; 8,9 BIS(BENZYLOXY) 10 PROPYL 3,4,5,8,9,10 HEXAHYDRO 2H OXECIN 2 ONE; [5,6 BIS(BENZYLOXY)OCT 7 EN 4 YLOXY]TERT BUTYLDIMETHYLSILANE; HERBARUMIN I; HERBICIDE; STAGONOLIDE A; UNCLASSIFIED DRUG;

ANTIFUNGAL ACTIVITY; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CLINICAL PROTOCOL; COLUMN CHROMATOGRAPHY; GRIGNARD REACTION; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; SYNTHESIS; TEMPERATURE;

EID: 77954616757     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0029-1218775     Document Type: Article

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