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
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Sprache:eng
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Zusammenfassung: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.
ISSN:2365-6549
2365-6549
DOI:10.1002/slct.202102759