Electrophilic α-thiocyanation of chiral and achiral N-acyl imides. A convenient route to 5-substituted and 5,5-disubstituted 2,4-thiazolidinediones

Bioorganic and Medicinal Chemistry Letters

Volumn 18, Issue 6, 2008, Pages 1768-1771

  Falck, J R ^a   Gao, Shuanhu ^a   Prasad, Ravi Naga ^a   Koduru, Sreenivasulu Reddy ^a  

^a UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

Author keywords

Asymmetric; Enolate; Heterocycle; Thiazolidinedione; Thiocyanate

Indexed keywords

2,4 THIAZOLIDINEDIONE DERIVATIVE; IMIDE; SUCCINIMIDE DERIVATIVE; THIOL GROUP;

ARTICLE; CHEMICAL REACTION; CHIRALITY; CYANATION; CYCLIZATION; DIASTEREOISOMER; HYDROLYSIS; QUANTUM YIELD; RACEMIZATION; REACTION ANALYSIS; STEREOCHEMISTRY;

CYCLIZATION; IMIDES; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; STEREOISOMERISM; THIAZOLIDINEDIONES; THIOCYANATES;

EID: 40949085205     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2008.02.034     Document Type: Article

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