AlCl3‐Catalyzed Synthesis of Triazolo[5,1‐b]thiazines

AlCl3‐Catalyzed oxidative cyclization of thiosemicarbazones / triazolothiones with propargylic alcohols is achieved to afford a diverse set of triazolothiazines in good yields. Triazolothiazines were synthesized in a shorter duration at room temperature under an open‐air environment with atom econom...

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Veröffentlicht in:	ChemistrySelect (Weinheim) 2021-10, Vol.6 (38), p.10258-10262
Hauptverfasser:	Muthusamy, Sengodagounder, Malarvizhi, Muthukumar, Suresh, Eringathodi
Format:	Artikel
Sprache:	eng
Schlagworte:	1,3-thiazine aluminium chloride propargylic alcohol thiosemicarbazone triazolothiazine
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creator	Muthusamy, Sengodagounder Malarvizhi, Muthukumar Suresh, Eringathodi
description	AlCl3‐Catalyzed oxidative cyclization of thiosemicarbazones / triazolothiones with propargylic alcohols is achieved to afford a diverse set of triazolothiazines in good yields. Triazolothiazines were synthesized in a shorter duration at room temperature under an open‐air environment with atom economical approach. AlCl3‐Catalyzed oxidative cyclization of thiosemicarbazones / triazolothiones with propargylic alcohols is achieved by providing a diverse set of triazolothiazines in good yields. Triazolothiazines were synthesized in a shorter duration at room temperature under an open‐air environment with atom economical approach.
doi_str_mv	10.1002/slct.202102759
format	Article
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subjects	1,3-thiazine aluminium chloride propargylic alcohol thiosemicarbazone triazolothiazine
title	AlCl3‐Catalyzed Synthesis of Triazolo[5,1‐b]thiazines
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