Stereoselective preparation of C1-C10 and C11-O14 fragments of narbonolide: Exploiting the versatility of thiazolidinethione chiral auxiliary

Synthesis

Volumn , Issue 3, 2009, Pages 474-482

  Narasimhulu, C Prasad ^a   Das, Parthasarathi ^a  

^a DR REDDY'S LABORATORIES LTD   (India)

Author keywords

Acyl thiazolidinethione; Aldol reaction; Crimmins protocol; Myers alkylation; Tebbe reaction

Indexed keywords

ACYL-THIAZOLIDINETHIONE; ALDOL REACTION; CRIMMINS PROTOCOL; MYERS ALKYLATION; TEBBE REACTION;

ALKYLATION; STEREOCHEMISTRY; STEREOSELECTIVITY;

HYDROCARBONS;

NARBONOLIDE; POLYKETIDE; THIAZOLIDINE DERIVATIVE; THIAZOLIDINETHIONE; UNCLASSIFIED DRUG;

ALDOL REACTION; ALKYLATION; CARBON NUCLEAR MAGNETIC RESONANCE; CHIRALITY; CONFERENCE PAPER; DRUG STRUCTURE; DRUG SYNTHESIS; ESTERIFICATION; PROTON NUCLEAR MAGNETIC RESONANCE; RING CLOSING METATHESIS; STEREOCHEMISTRY;

EID: 63849329428     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0028-1083321     Document Type: Conference Paper

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