A concise stereoselective total synthesis of synargentolide a from 3,4,6-Tri- O -acetyl- D -glucal

Synthesis

Volumn , Issue 8, 2011, Pages 1279-1282

  Sabitha, Gowravaram ^a   Reddy, S Siva Sankara ^a   Raju, Atla ^a   Yadav, Jhillu S ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

3,4,6 tri O acetyl D glucal; browns allylation; D lactones; RCM; synargentolide

Indexed keywords

3,4,6-TRI-O-ACETYL-D-GLUCAL; ASYMMETRIC ALLYLATION; BROWNS ALLYLATION; NATURALLY OCCURRING; RCM; RING-CLOSING METATHESIS REACTIONS; STARTING MATERIALS; STEREO-SELECTIVE; STEREOSELECTIVE SYNTHESIS; SYNARGENTOLIDE; TOTAL SYNTHESIS;

ALLYLATION; CLIMATE MODELS; STEREOSELECTIVITY;

SYNTHESIS (CHEMICAL);

3,4,6, TRI ORTHO ACETYL DEXTRO GLUCAL; CHEMICAL COMPOUND; LACTONE DERIVATIVE; NATURAL PRODUCT; SYNARGENTOLIDE A; UNCLASSIFIED DRUG;

ALLYLATION; ARTICLE; CHEMICAL ANALYSIS; CHEMICAL INTERACTION; CHEMICAL STRUCTURE; CHIRALITY; RING CLOSING METATHESIS; STEREOCHEMISTRY; SYNTHESIS;

EID: 79953768911     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1258458     Document Type: Article

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