Literature DB >> 17888660

Convenient method for the addition of disulfides to alkenes.

Noriyuki Yamagiwa1, Yutaka Suto, Yasuhiro Torisawa.   

Abstract

Catalytic disulfenylation reaction of alkenes by common Lewis acids has been investigated in detail. While reactions by FeCl(3) were feasible with cycloalkenes and other simple alkenes, much faster and excellent conversions were possible by AlCl(3) even with the substrates less reactive toward FeCl(3).

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Year:  2007        PMID: 17888660     DOI: 10.1016/j.bmcl.2007.09.021

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

1.  Silica: An efficient catalyst for one-pot regioselective synthesis of dithioethers.

Authors:  Samir Kundu; Babli Roy; Basudeb Basu
Journal:  Beilstein J Org Chem       Date:  2014-01-07       Impact factor: 2.883

2.  Disulfide-yne reaction: controlling the reactivity of a surface by light.

Authors:  Yuwen Li; Sen Li; Xin Du; Zhongze Gu
Journal:  RSC Adv       Date:  2021-06-14       Impact factor: 3.361

  2 in total

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