Thiourea to bicyclic scaffolds: highly regio- and stereoselective routes to dithiazolopyrimidines

Tetrahedron

Volumn 63, Issue 29, 2007, Pages 6924-6931

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

^a UNIVERSITY OF ALLAHABAD   (India)

Author keywords

Diastereoselective synthesis; Dithiazolopyrimidines; Michael addition; Microwaves; Thiourea

Indexed keywords

BICYCLO COMPOUND; DITHIAZOLOPYRIMIDINE DERIVATIVE; METHANSULFINYLMETHYLISOTHIOUREA; OXAZOLONE; PYRIMIDINE DERIVATIVE; UNCLASSIFIED DRUG; UREA DERIVATIVE;

ADDITION REACTION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; CYCLIZATION; DEMETHYLATION; MICHAEL ADDITION; MICROWAVE IRRADIATION; NUCLEAR OVERHAUSER EFFECT; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STEREOCHEMISTRY; STRUCTURE ANALYSIS;

EID: 34249808835     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.04.033     Document Type: Article

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