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I2-mediated Csp2-P bond formation via tandem cyclization of o-alkynylphenyl isothiocyanates with organophosphorus esters.
Liu, Yang; Wu, Wenjin; Sang, Xiaoyan; Xia, Yu; Fang, Guojian; Hao, Wenyan.
Afiliação
  • Liu Y; College of Chemistry and Chemical Engineering, Jiangxi Normal University Nanchang 330022 People's Republic of China wenyanhao@jxnu.edu.cn.
  • Wu W; College of Chemistry and Chemical Engineering, Jiangxi Normal University Nanchang 330022 People's Republic of China wenyanhao@jxnu.edu.cn.
  • Sang X; College of Chemistry and Chemical Engineering, Jiangxi Normal University Nanchang 330022 People's Republic of China wenyanhao@jxnu.edu.cn.
  • Xia Y; College of Chemistry and Chemical Engineering, Jiangxi Normal University Nanchang 330022 People's Republic of China wenyanhao@jxnu.edu.cn.
  • Fang G; College of Chemistry and Chemical Engineering, Jiangxi Normal University Nanchang 330022 People's Republic of China wenyanhao@jxnu.edu.cn.
  • Hao W; College of Chemistry and Chemical Engineering, Jiangxi Normal University Nanchang 330022 People's Republic of China wenyanhao@jxnu.edu.cn.
RSC Adv ; 12(28): 18072-18076, 2022 Jun 14.
Article em En | MEDLINE | ID: mdl-35800309
ABSTRACT
A novel, I2-mediated tandem cyclization of o-alkynylphenyl isothiocyanates with organophosphorus esters has been developed under mild conditions. Different kinds of 4H-benzo[d][1,3]thiazin-2-ylphosphonate could be synthesized in moderate to excellent yields. This method has the advantages of easy access to raw materials, free-metal catalyst, simple operation, high yield and high functional group tolerance.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article