| Literature DB >> 15876118 |
Feng Xu1, Weifeng Shi, Jianbo Wang.
Abstract
[reaction: see text] A series of beta-thio group substituted alpha-diazo carbonyl compounds have been prepared by nucleophilic substitution reactions of thiophenol, thionaphthol, or benzyl mercaptan with beta-acetoxy-alpha-diazo carbonyl compounds. The diazo decomposition of these diazo carbonyl compounds with various transition metal catalysts, including Rh(II) carboxylates and Cu(I) and Cu(II) complexes, has been investigated. It was found that the diazo decomposition of these compounds gave 1,2-thio group migration products. No 1,2-hydride or 1,2-aryl migration products were observed in all cases.Entities:
Year: 2005 PMID: 15876118 DOI: 10.1021/jo050109v
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354