Affiliation:
1. Synthetic Organic Chemistry Division, Regional Research Laboratory, Jorhat-785 006, India
2. Medicinal Aromatic and Economic plant Division, Regional Research Laboratory, Jorhat-785 006, India
Abstract
2-Benzylidineamino-4-phenyl-1,3-thiazole undergoes [4+2] Diels–Alder cycloaddition reaction with sulfene resulting in good yield of a mixture of isomeric 2,6-diphenyl-2H,4H-[1,3]thiazolo[3,2-c][1,3,5]thiadiazine 3,3-dioxides and 3, 7-diphenyl[1,3]thiazolo[3,2-b] [1,2,4]thiadiazine 5,5-dioxides derivatives are reported.
Cited by
7 articles.
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1. Synthesis of some novel 7‐substituted [1,3,4]thiadiazolo[3,2‐
c
][1,3,5]thiadiazine‐6,6‐dioxides with antifungal evaluation against rice pathogens;Journal of Heterocyclic Chemistry;2020-10-11
2. Synthesis and antifungal activities of 3,5‐diphenyl‐7‐amino‐[1,3]‐thiazolo[3,2‐a]pyrimidine‐6‐nitrile derivatives;Journal of Heterocyclic Chemistry;2020-01-10
3. Exploration and Optimization of an Efficient One-pot Sequential Synthesis of Di/tri-substituted Thiazoles from α-Bromoketones, Thioacids Salt, and Ammonium Acetate;Journal of Heterocyclic Chemistry;2015-08-07
4. Synthesis and Antibacterial Activity of 4-Aryl-2-(1-substituted ethylidene)thiazoles;Archiv der Pharmazie;2013-06-17
5. Diels-Alder Reaction;Comprehensive Organic Name Reactions and Reagents;2010-09-15