N-thioaroylmorpholines in silica gel-water: An efficient system to access functionalized allylic thioesters from baylis-hillman bromides

Synthesis

Volumn , Issue 8, 2011, Pages 1261-1266

  Patel, Rajesh ^a   Srivastava, Vishnu P ^a   Yadav, Lal Dhar S ^a  

^a UNIVERSITY OF ALLAHABAD   (India)

Author keywords

allylic thioesters; aqueous medium; Baylis hillman adducts; green chemistry; nucleophilic displacement; regioselectivity

Indexed keywords

AQUEOUS MEDIUM; BAYLIS-HILLMAN ADDUCTS; GREEN CHEMISTRY; NUCLEOPHILIC DISPLACEMENT; THIOESTERS;

CATALYSTS; DRIERS (MATERIALS); REGIOSELECTIVITY; SILICA; SILICA GEL; SULFUR; SULFUR COMPOUNDS; SYNTHESIS (CHEMICAL);

BROMINE COMPOUNDS;

ALLYL COMPOUND; ALLYLIC THIOESTER DERIVATIVE; BROMINE DERIVATIVE; MORPHOLINE DERIVATIVE; N THIOAROYLMORPHOLINE DERIVATIVE; SILICA GEL; THIOESTER; UNCLASSIFIED DRUG; WATER;

ALKYLATION; ARTICLE; BAYLIS HILLMAN REACTION; CATALYST; CHEMICAL ANALYSIS; CHEMICAL INTERACTION; CHEMICAL STRUCTURE; HYDROLYSIS; NUCLEOPHILICITY; STEREOCHEMISTRY; SYNTHESIS;

EID: 79953805439     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1258476     Document Type: Article

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