An odorless thia-Michael addition using Bunte salts as thiol surrogates

Autor:	Chun Cai, Ya-mei Lin, Wen-Bin Yi, Guo-ping Lu
Rok vydání:	2015
Předmět:	chemistry.chemical_classification chemistry.chemical_compound chemistry General Chemical Engineering Thiol Michael reaction Organic chemistry Halide General Chemistry Sodium thiosulfate Bond formation
Zdroj:	RSC Advances. 5:27107-27111
ISSN:	2046-2069
DOI:	10.1039/c5ra01381j
Popis:	A newly developed C–S bond formation process via acid-catalyzed thia-Michael addition has been demonstrated. The protocol, in which Bunte salts generated from odorless and inexpensive sodium thiosulfate and organic halides are used as the thiol precursors, provides an efficient approach for the synthesis of β-sulfido carbonyl compounds.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::34be52f239beb3aaf786340698bfad84 https://doi.org/10.1039/c5ra01381j Zobrazit plný text záznamu