Literature DB >> 29637310

Sulfur-Sulfur Bond Construction.

Ming Wang1, Xuefeng Jiang2.   

Abstract

Disulfide, as a common structural motif, has been frequently used in pharmaceuticals, nature products, and chemical biology. This chapter focuses on the methodologies that were reported recently for the synthesis of disulfide-containing compounds with particular emphasis on the synthesis of unsymmetrical disulfides. The presentation is organized according to the structure of the disulfides and the synthetic method.

Entities:  

Keywords:  ADC; Disulfide; Natural products; Pharmaceuticals

Year:  2018        PMID: 29637310     DOI: 10.1007/s41061-018-0192-5

Source DB:  PubMed          Journal:  Top Curr Chem (Cham)        ISSN: 2364-8961


  3 in total

1.  Novel Cyclic Biphalin Analogues by Ruthenium-Catalyzed Ring Closing Metathesis: in Vivo and in Vitro Biological Profile.

Authors:  Azzurra Stefanucci; Wei Lei; Stefano Pieretti; Marilisa Pia Dimmito; Grazia Luisi; Ettore Novellino; Michał Nowakowski; Wiktor Koźmiński; Sako Mirzaie; Gokhan Zengin; John M Streicher; Adriano Mollica
Journal:  ACS Med Chem Lett       Date:  2019-03-08       Impact factor: 4.345

2.  Decatungstate-catalyzed radical disulfuration through direct C-H functionalization for the preparation of unsymmetrical disulfides.

Authors:  Jingjing Zhang; Armido Studer
Journal:  Nat Commun       Date:  2022-07-06       Impact factor: 17.694

3.  Visible-Light-Mediated Three-Component Cascade Sulfonylative Annulation.

Authors:  Ganesh Chandra Upreti; Tavinder Singh; Sudhir Ranjan; Raju Kumar Gupta; Anand Singh
Journal:  ACS Omega       Date:  2022-08-18
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.