cheminform abstract: procedure-controlled selective synthesis of 5-acyl-2-iminothiazolines and their...

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ChemInform 2012, 43, issue 02 © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Thiazole derivatives R 0260 DOI: 10.1002/chin.201202135 Procedure-Controlled Selective Synthesis of 5-Acyl-2-iminothiazolines and Their Selenium and Tellurium Derivatives by Convergent Tandem Annulation. — A selective synthesis of 5-acyl-2-iminothiazoles (IV) and their analogues (VI) is achieved via reaction of carbodiimides with carboxylic acid chlorides followed by treatment with lithiated chalcogenoalkynes. — (WANG, Y.; ZHANG*, W.-X.; WANG, Z.; XI, Z.; Angew. Chem., Int. Ed. 50 (2011) 35, 8122-8126, http://dx.doi.org/10.1002/anie.201101948 ; Beijing Natl. Lab. Mol. Sci., Coll. Chem., Peking Univ., Beijing 100871, Peop. Rep. China; Eng.) — Mais 02- 135

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Page 1: ChemInform Abstract: Procedure-Controlled Selective Synthesis of 5-Acyl-2-iminothiazolines and Their Selenium and Tellurium Derivatives by Convergent Tandem Annulation

Thiazole derivativesR 0260 DOI: 10.1002/chin.201202135

Procedure-Controlled Selective Synthesis of 5-Acyl-2-iminothiazolines and Their Selenium and Tellurium Derivatives by Convergent Tandem Annulation. — A selective synthesis of 5-acyl-2-iminothiazoles (IV) and their analogues (VI) is achieved via reaction of carbodiimides with carboxylic acid chlorides followed by treatment with lithiated chalcogenoalkynes. — (WANG, Y.; ZHANG*, W.-X.; WANG, Z.; XI, Z.; Angew. Chem., Int. Ed. 50 (2011) 35, 8122-8126, http://dx.doi.org/10.1002/anie.201101948 ; Beijing Natl. Lab. Mol. Sci., Coll. Chem., Peking Univ., Beijing 100871, Peop. Rep. China; Eng.) — Mais

02- 135

ChemInform 2012, 43, issue 02 © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim