Selective Bromination of 4,5-Dimethylthiazole withN-Bromosuccinimide
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/(SICI)1099-0690(199804)1998:4%3C593::AID-EJOC593%3E3.0.CO;2-F/fullpdf
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2. Indolo-2,3-quinodimethanes and stable cyclic analogs for regio- and stereocontrolled syntheses of [b]-annelated indoles
3. Free radical chlorination of methyl derivatives of pyridine, pyrazine, and thiazole by N-chlorosuccinimide
4. The Preparation of Thiazole Grignard Reagents and Thiazolyllithium Compounds1,2
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1. Microwave-assisted synthesis of new fluorescent indoline-based building blocks by ligand free Suzuki-Miyaura cross-coupling reaction in aqueous media;Tetrahedron;2016-06
2. Synthesis of Heterocyclic Analogs of α-aminoadipic Acid and its Esters Based on Imidazo[2,1-b][1,3]Thiazole;Journal of Heterocyclic Chemistry;2014-06-11
3. Regioselective Bromination of a Thymine–Acridine Conjugate by N-Bromosuccinimide;Synthetic Communications;2010-03-19
4. Highly regioselective direct halogenation: a simple and efficient method for preparing 4-halomethyl-5-methyl-2-aryl-1,3-thiazoles;Tetrahedron Letters;2004-01
5. A computational approach of the selective free-radical bromination of 4,5-dimethyl-thiazole with N -bromosuccinimide;Journal of Molecular Structure: THEOCHEM;2000-03
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