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Iodine-mediated synthesis of 3-acylbenzothiadiazine 1,1-dioxides

An iodine-mediated synthesis of 3-acylbenzothiadizine 1,1-dioxides is described. A range of electronically diverse acetophenones reacted well with several 2-aminobenzenesulfonamides, affording 3-acylbenzothiadiazine 1,1-dioxides in good yields.

Detalles Bibliográficos
Autores principales: Xi, Long-Yi, Zhang, Ruo-Yi, Shi, Lei, Chen, Shan-Yong, Yu, Xiao-Qi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902049/
https://www.ncbi.nlm.nih.gov/pubmed/27340493
http://dx.doi.org/10.3762/bjoc.12.101
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author Xi, Long-Yi
Zhang, Ruo-Yi
Shi, Lei
Chen, Shan-Yong
Yu, Xiao-Qi
author_facet Xi, Long-Yi
Zhang, Ruo-Yi
Shi, Lei
Chen, Shan-Yong
Yu, Xiao-Qi
author_sort Xi, Long-Yi
collection PubMed
description An iodine-mediated synthesis of 3-acylbenzothiadizine 1,1-dioxides is described. A range of electronically diverse acetophenones reacted well with several 2-aminobenzenesulfonamides, affording 3-acylbenzothiadiazine 1,1-dioxides in good yields.
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spelling pubmed-49020492016-06-23 Iodine-mediated synthesis of 3-acylbenzothiadiazine 1,1-dioxides Xi, Long-Yi Zhang, Ruo-Yi Shi, Lei Chen, Shan-Yong Yu, Xiao-Qi Beilstein J Org Chem Full Research Paper An iodine-mediated synthesis of 3-acylbenzothiadizine 1,1-dioxides is described. A range of electronically diverse acetophenones reacted well with several 2-aminobenzenesulfonamides, affording 3-acylbenzothiadiazine 1,1-dioxides in good yields. Beilstein-Institut 2016-05-24 /pmc/articles/PMC4902049/ /pubmed/27340493 http://dx.doi.org/10.3762/bjoc.12.101 Text en Copyright © 2016, Xi et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Xi, Long-Yi
Zhang, Ruo-Yi
Shi, Lei
Chen, Shan-Yong
Yu, Xiao-Qi
Iodine-mediated synthesis of 3-acylbenzothiadiazine 1,1-dioxides
title Iodine-mediated synthesis of 3-acylbenzothiadiazine 1,1-dioxides
title_full Iodine-mediated synthesis of 3-acylbenzothiadiazine 1,1-dioxides
title_fullStr Iodine-mediated synthesis of 3-acylbenzothiadiazine 1,1-dioxides
title_full_unstemmed Iodine-mediated synthesis of 3-acylbenzothiadiazine 1,1-dioxides
title_short Iodine-mediated synthesis of 3-acylbenzothiadiazine 1,1-dioxides
title_sort iodine-mediated synthesis of 3-acylbenzothiadiazine 1,1-dioxides
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902049/
https://www.ncbi.nlm.nih.gov/pubmed/27340493
http://dx.doi.org/10.3762/bjoc.12.101
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