Palladium-Catalyzed Sulfinylation of Aryl- And Alkenylborons with Sulfinate Esters

9Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

Abstract

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.

Cite

CITATION STYLE

APA

Suzuki, M., Kanemoto, K., Nakamura, Y., Hosoya, T., & Yoshida, S. (2021). Palladium-Catalyzed Sulfinylation of Aryl- And Alkenylborons with Sulfinate Esters. Organic Letters, 23(9), 3793–3797. https://doi.org/10.1021/acs.orglett.1c01292

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free