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Metal-Free Highly Regioselective 1,4-Sulfonyliodination of 1,3-Enynes.
Lv, Yunhe; Lai, Junrong; Pu, Weiya; Wang, Jin; Han, Wanru; Wang, Axue; Zhang, Mengyue; Wang, Xue.
Afiliação
  • Lv Y; College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang 455000, P. R. China.
  • Lai J; College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang 455000, P. R. China.
  • Pu W; College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang 455000, P. R. China.
  • Wang J; College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang 455000, P. R. China.
  • Han W; College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang 455000, P. R. China.
  • Wang A; College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang 455000, P. R. China.
  • Zhang M; College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang 455000, P. R. China.
  • Wang X; College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang 455000, P. R. China.
J Org Chem ; 88(4): 2034-2045, 2023 Feb 17.
Article em En | MEDLINE | ID: mdl-36749192
ABSTRACT
Herein, a novel, practical, and green synthetic method using readily available 1,3-enynes with sulfonyl hydrazides and I2 through tert-butyl hydroperoxide (TBHP)-mediated 1,4-sulfonyliodination has been developed for synthesizing various tetrasubstituted allenyl iodides under metal-free conditions. Notably, the proposed method exhibits a broad substrate scope, operational simplicity, tolerance to air, high functional-group tolerance, satisfactory yields, and excellent regioselectivity as well as involves the use of cost-effective reagents such as green oxidants.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article