Literature DB >> 23846983

Transfer of sulfur: from simple to diverse.

Hui Liu1, Xuefeng Jiang.   

Abstract

The introduction of sulfur atoms onto target molecules is an important area in organic synthesis, in particular in the synthesis of pharmaceutical compounds, and a wide variety of sulfuration agents have been developed for thionation reactions over the past few decades. In this Focus Review, we collect and summarize the C-S bond-formation reactions that have been used to construct C-S bonds in natural products and pharmaceutical compounds.
Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  cross-coupling; drug design; heterocycles; natural products; sulfur

Mesh:

Substances:

Year:  2013        PMID: 23846983     DOI: 10.1002/asia.201300636

Source DB:  PubMed          Journal:  Chem Asian J        ISSN: 1861-471X


  22 in total

1.  Metal-free Chlorothiolation of Alkenes using HCl and Sulfoxides.

Authors:  Rene Ebule; Gerald B Hammond; Bo Xu
Journal:  European J Org Chem       Date:  2018-07-19

2.  A 5 + 1 Protic Acid Assisted Aza-Pummerer Approach for Synthesis of 4-Chloropiperidines from Homoallylic Amines.

Authors:  Rene Ebule; Sagar Mudshinge; Michael H Nantz; Mark S Mashuta; Gerald B Hammond; Bo Xu
Journal:  J Org Chem       Date:  2019-02-27       Impact factor: 4.354

3.  Organophotoredox-Catalyzed Formation of Alkyl-Aryl and -Alkyl C-S/Se Bonds from Coupling of Redox-Active Esters with Thio/Selenosulfonates.

Authors:  Yue Dong; Peng Ji; Yueteng Zhang; Changqing Wang; Xiang Meng; Wei Wang
Journal:  Org Lett       Date:  2020-12-10       Impact factor: 6.005

4.  Dual gold and photoredox catalysis: visible light-mediated intermolecular atom transfer thiosulfonylation of alkenes.

Authors:  Haoyu Li; Cuicui Shan; Chen-Ho Tung; Zhenghu Xu
Journal:  Chem Sci       Date:  2017-01-04       Impact factor: 9.825

5.  Polysulfurating reagent design for unsymmetrical polysulfide construction.

Authors:  Xiao Xiao; Jiahui Xue; Xuefeng Jiang
Journal:  Nat Commun       Date:  2018-06-06       Impact factor: 14.919

6.  Nickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides.

Authors:  Yi Fang; Torben Rogge; Lutz Ackermann; Shun-Yi Wang; Shun-Jun Ji
Journal:  Nat Commun       Date:  2018-06-08       Impact factor: 14.919

7.  Unexpected Substituent Effects in Spiro-Compound Formation: Steering N-Aryl Propynamides and DMSO toward Site-Specific Sulfination in Quinolin-2-ones or Spiro[4,5]trienones.

Authors:  Xiaoxian Li; Yuanxun Wang; Yaxin Ouyang; Zhenyang Yu; Beibei Zhang; Jingran Zhang; Haofeng Shi; Han Zuilhof; Yunfei Du
Journal:  J Org Chem       Date:  2021-06-29       Impact factor: 4.354

8.  Synthesis of β-Hydroxysulfides from Thiophenols and Disulfides with tert-Butyl Hydroperoxide as the Oxidant and Reactant.

Authors:  Jian-Bo Feng; Xiao-Feng Wu
Journal:  ChemistryOpen       Date:  2016-05-17       Impact factor: 2.911

9.  Exact mass analysis of sulfur clusters upon encapsulation by a polyaromatic capsular matrix.

Authors:  Sho Matsuno; Masahiro Yamashina; Yoshihisa Sei; Munetaka Akita; Akiyoshi Kuzume; Kimihisa Yamamoto; Michito Yoshizawa
Journal:  Nat Commun       Date:  2017-09-29       Impact factor: 14.919

10.  Indium-Catalyzed Direct Conversion of Lactones into Thiolactones Using a Disilathiane as a Sulfur Source.

Authors:  Yohei Ogiwara; Ken Takano; Shuhei Horikawa; Norio Sakai
Journal:  Molecules       Date:  2018-06-02       Impact factor: 4.411

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