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  • Rhodium-catalyzed asymmetric conjugate addition of arylboronic acids to nitroalkenes using olefin-sulfoxide ligands.

Rhodium-catalyzed asymmetric conjugate addition of arylboronic acids to nitroalkenes using olefin-sulfoxide ligands.

The Journal of organic chemistry (2012-03-27)
Feng Xue, Dongping Wang, Xincheng Li, Boshun Wan
ABSTRACT

An efficient rhodium/olefin-sulfoxide catalyzed asymmetric conjugate addition of organoboronic acids to a variety of nitroalkenes has been developed, where 2-methoxy-1-naphthyl sulfinyl functionalized olefin ligands have shown to be highly effective and are applicable to a broad scope of aryl, alkyl, and heteroaryl nitroalkenes.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
p-Tolylboronic acid, 97%
Sigma-Aldrich
4-Methoxyphenylboronic acid, ≥95.0%
Sigma-Aldrich
4-Fluorophenylboronic acid, ≥95%