Rhodium-catalyzed asymmetric conjugate addition of arylboronic acids to nitroalkenes using olefin-sulfoxide ligands.
Feng Xue, Dongping Wang, Xincheng Li, Boshun Wan
Index: J. Org. Chem. 7th ed., 77 , 3071-3081, (2012)
Full Text: HTML
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.
Related Compounds
Related Articles:
2009-05-15
[Bioorg. Med. Chem. Lett. 19 , 2642-5, (2009)]
Direct palladium(II)-catalyzed synthesis of arylamidines from aryltrifluoroborates.
2012-05-04
[Org. Lett. 9th ed., 14 , 2394-2397, (2012)]
Ruthenium(0)-catalyzed sp3 C-H bond arylation of benzylic amines using arylboronates.
2012-04-06
[Org. Lett. 7th ed., 14 , 1930-1933, (2012)]
2012-05-07
[Chem. Commun. (Camb.) 36th ed., 48 , 4332-4334, (2012)]
Aryl boronic acid inhibition of synthetic melanin polymerization.
2010-08-01
[Bioorg. Med. Chem. Lett. 20 , 4475-8, (2010)]