z-logo
open-access-imgOpen Access
Palladium-Catalyzed Sulfinylation of Aryl- and Alkenylborons with Sulfinate Esters
Author(s) -
Minori Suzuki,
Kazuya Kanemoto,
Yu Nakamura,
Takamitsu Hosoya,
Suguru Yoshida
Publication year - 2021
Publication title -
organic letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.94
H-Index - 239
eISSN - 1523-7060
pISSN - 1523-7052
DOI - 10.1021/acs.orglett.1c01292
Subject(s) - organosulfur compounds , palladium , chemistry , aryl , sulfoxide , catalysis , organic chemistry , sulfone , combinatorial chemistry , sulfur , alkyl
An efficient, direct sulfinylation of organoborons catalyzed by palladium is disclosed. Treatment of organoborons and sulfinate esters in the presence of a palladium precatalyst provided a broad range of sulfoxides. Various organosulfur compounds having oxidizable functional groups were successfully prepared through the sulfoxide synthesis.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom