The Organophosphorus Sulfenyl Bromides as Versatile Reagents for Cysteine Derivatives Functionalization by Unsymmetrical Disulfide Bond Formation
Author:
Affiliation:
1. a Department of Organic Chemistry, Chemical Faculty , Gdansk University of Technology , Gdansk, Poland
Publisher
Informa UK Limited
Subject
Inorganic Chemistry,Organic Chemistry,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/10426500701735437
Reference10 articles.
1. New, efficient and chemoselective method of thioacylation, starting from carboxylic acids
2. Synthesis of S-thioacyl dithiophosphates, efficient and chemoselective thioacylating agentsProofs for the reversibility of isomerisation of anhydrides 1 to 2, melting points of amides and thioamides obtained from anhydrides 5–7 and 1H, 13C NMR and IR data of isolated anhydrides 5–7, 17 are available as supplementary data. For direct access, see http://www.rsc.org/suppdata/p1/b2/b201233b/
3. New reaction of dithiophosphoric acids with O-thioacylhydroxylamines. Nucleophilic substitution or single electron transfer process?
4. S-Thioacyldithiophosphates in the Synthesis of Thiohydroxamic Acids and O-Thioacylhydroxylamines
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1. A quantum chemical study of the gas-phase homolytic S–Br bond dissociation enthalpies of sulfenyl bromides;Chemical Data Collections;2020-08
2. A convenient method for the preparation of functionalizedN-acylsulfenamides from primary amides;Phosphorus, Sulfur, and Silicon and the Related Elements;2016-02-01
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