First stereoselective total synthesis of cryptomoscatone D2 and syntheses of (5 R,7 S)-kurzilactone and (+)-cryptofolione by an asymmetric acetate aldol approach

Synthesis

Volumn 44, Issue 9, 2012, Pages 1365-1372

  Yadav, Jhillusingh ^a   Ganganna, Bogonda ^a   Bhunia, Dineshchandra ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

aldol reactions; cyclizations; lactones; stereoselective synthesis; total synthesis

Indexed keywords

ALDOL REACTIONS; CYCLIZATIONS; LACTONES; STEREOSELECTIVE SYNTHESIS; TOTAL SYNTHESIS;

ALDEHYDES; CONDENSATION REACTIONS; STEREOCHEMISTRY; VOLATILE FATTY ACIDS;

STEREOSELECTIVITY;

5,7 KURZILACTONE; ACETIC ACID; CINNAMALDEHYDE; CRYPTOFOLIONE; CRYPTOMOSCATONE D2; PYRONE DERIVATIVE; UNCLASSIFIED DRUG;

ALDOL REACTION; ALLYLATION; ARTICLE; ASYMMETRIC SYNTHESIS; DRUG STRUCTURE; DRUG SYNTHESIS; HORNER WADSWORTH EMMONS REACTION; RING CLOSING METATHESIS; STEREOCHEMISTRY;

EID: 84859384945     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0031-1290771     Document Type: Article

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