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Di-tert-butyl peroxide-mediated atom-transfer radical addition of 2-chlorodithiane to aryl alkynes under mild conditions.
Lai, Junshan; Tian, Lixia; Liang, Yongping; Zhang, Yuan; Xie, Xingang; Fang, Bowen; Tang, Shouchu.
Afiliação
  • Lai J; School of Pharmacy, Lanzhou University, Lanzhou 730000 (P. R. China).
  • Tian L; School of Pharmacy, Lanzhou University, Lanzhou 730000 (P. R. China).
  • Liang Y; School of Pharmacy, Lanzhou University, Lanzhou 730000 (P. R. China).
  • Zhang Y; State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000 (P. R. China).
  • Xie X; State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000 (P. R. China).
  • Fang B; Chemical Engineering Institute, Northwest University for Nationalities, Lanzhou, 730030 (P. R. China).
  • Tang S; School of Pharmacy, Lanzhou University, Lanzhou 730000 (P. R. China). tangshch@lzu.edu.cn.
Chemistry ; 21(41): 14328-31, 2015 Oct 05.
Article em En | MEDLINE | ID: mdl-26296151
ABSTRACT
Atom transfer radical addition (ATRA) of 2-chlorodithiane onto aryl alkynes through the use of di-tert-butyl peroxide as an oxidant at room temperature directly affords a variety of synthetically valuable ß-chloro-(Z)-vinyl dithianes in good yields with high regioselectivities and without the assistance of any transition metals. It provides an operationally simple pathway to access vinyl dithianes with controlled formation of a new C(sp(2) )C bond and a C(sp(2) )Cl bond.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chemistry Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chemistry Ano de publicação: 2015 Tipo de documento: Article