The first regio- and diastereoselective direct introduction of α-mercaptoacetic acid/amide units into Morita-Baylis-Hillman acetates

Tetrahedron Letters

Volumn 50, Issue 20, 2009, Pages 2414-2419

  Yadav, Lal Dhar S ^a   Rai, Viaji K ^a  

^a UNIVERSITY OF ALLAHABAD   (India)

Author keywords

Mercapto acids; Mercapto amides; Diastereoselective synthesis; Morita Baylis Hillman reaction; Regioselective; SN2 reaction

Indexed keywords

1,3 OXATHIOLANE DERIVATIVE; 1,4 DIAZABICYCLO[2.2.2]OCTANE; ACETIC ACID DERIVATIVE; ALPHA MERCAPTOACETIC ACID; AMIDE; CERIUM; THIOGLYCOLIC ACID DERIVATIVE; UNCLASSIFIED DRUG;

AMINOLYSIS; ARTICLE; BAYLIS HILLMAN REACTION; DIASTEREOISOMER; ENVIRONMENTAL TEMPERATURE; HYDROLYSIS; STEREOCHEMISTRY; SUBSTITUTION REACTION;

EID: 63349110161     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.03.016     Document Type: Article

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