B(C6F5)3‑Catalyzed Hydrodesulfurization Using Hydrosilanes – Metal-Free Reduction of Sulfides

B­(C6F5)3-catalyzed hydrodesulfurization of carbon–sulfur bonds was achieved using triethylsilane as the reducing agent. The corresponding products were obtained in good yields under mild reaction conditions. This protocol could be applied to the reduction of sulfides, including benzyl and alkyl sul...

Full description

Saved in:
Bibliographic Details
Published inOrganic letters Vol. 17; no. 13; pp. 3366 - 3369
Main Authors Saito, Kodai, Kondo, Kazumi, Akiyama, Takahiko
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 02.07.2015
Online AccessGet full text

Cover

Loading…
More Information
Summary:B­(C6F5)3-catalyzed hydrodesulfurization of carbon–sulfur bonds was achieved using triethylsilane as the reducing agent. The corresponding products were obtained in good yields under mild reaction conditions. This protocol could be applied to the reduction of sulfides, including benzyl and alkyl sulfides and dithianes, with high chemoselectivities.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.5b01651