Cargando…
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.
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 |
Ejemplares similares
-
Facile synthesis of benzothiadiazine 1,1-dioxides, a precursor of RSV inhibitors, by tandem amidation/intramolecular aza-Wittig reaction
por: Majumdar, Krishna C, et al.
Publicado: (2013) -
Anion receptors containing thiazine-1,1-dioxide heterocycles as hydrogen bond donors
por: Wang, Hong-Bo, et al.
Publicado: (2010) -
Recyclable hypervalent-iodine-mediated solid-phase peptide synthesis and cyclic peptide synthesis
por: Liu, Dan, et al.
Publicado: (2018) -
Controlling hazardous chemicals in microreactors: Synthesis with iodine azide
por: Brandt, Johan C, et al.
Publicado: (2009) -
Iodine(III)-mediated halogenations of acyclic monoterpenoids
por: Peilleron, Laure, et al.
Publicado: (2018)