A mild and efficient stereoselective synthesis of (Z)- and (E)-allyl sulfides and potent antifungal agent, (Z)-3-(4-methoxybenzylidene)thiochroman-4- one from Morita-Baylis-Hillman acetates

Chemical and Pharmaceutical Bulletin

Volumn 55, Issue 8, 2007, Pages 1274-1276

  Das, Biswanath ^a   Chowdhury, Nikhil ^a   Damodar, Kongara ^a   Banerjee, Joydeep ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

(E) allyl sulfide; (Z) 3 (4 methoxybenzylidene) thiochroman 4 one; (Z) allyl sulfide; Antifungal compound; Benzene thiol; Morita Baylis Hillman acetate

Indexed keywords

3 (4 METHOXYBENZYLIDENE)THIOCHROMAN 4 ONE; ACETIC ACID DERIVATIVE; ANTIFUNGAL AGENT; BENZENE DERIVATIVE; CHROMAN DERIVATIVE; DIMETHYL SULFOXIDE; SODIUM HYDROXIDE; SULFIDE; TETRABUTYLAMMONIUM; THIOL DERIVATIVE; UNCLASSIFIED DRUG;

AQUEOUS SOLUTION; ARTICLE; BAYLIS HILLMAN REACTION; DRUG POTENCY; DRUG SYNTHESIS; ISOMER; ONE POT SYNTHESIS; ROOM TEMPERATURE; STEREOCHEMISTRY;

ACETATES; ALLYL COMPOUNDS; ANTIFUNGAL AGENTS; CATALYSIS; CHROMANS; CYCLIZATION; DIMETHYL SULFOXIDE; INDICATORS AND REAGENTS; MAGNETIC RESONANCE SPECTROSCOPY; SODIUM HYDROXIDE; SOLVENTS; SPECTROMETRY, MASS, FAST ATOM BOMBARDMENT; SPECTROPHOTOMETRY, INFRARED; STEREOISOMERISM; SULFIDES;

EID: 34548315880     PISSN: 00092363     EISSN: 13475223     Source Type: Journal    
DOI: 10.1248/cpb.55.1274     Document Type: Article

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