1245819-91-3Relevant academic research and scientific papers
Rhodium-catalyzed asymmetric conjugate addition of arylboronic acids to nitroalkenes using olefin-sulfoxide ligands
Xue, Feng,Wang, Dongping,Li, Xincheng,Wan, Boshun
experimental part, p. 3071 - 3081 (2012/05/04)
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 a
Rhodium-catalyzed asymmetric conjugate addition of organoboronic acids to nitroalkenes using chiral bicyclo [3.3.0] diene ligands
Wang, Zhi-Qian,Feng, Chen-Guo,Zhang, Shu-Sheng,Xu, Ming-Hua,Lin, Guo-Qiang
supporting information; experimental part, p. 5780 - 5783 (2010/10/21)
(Figure Presented) Old before l diene: An efficient rhodium/ diene-catalyzed asymmetric conjugate addition of organoboronic acids to challenging nitroalkene substrates that lack α substituents has been developed. Chiral bicyclo[3.3.0] dienes were found to
