34188-57-3Relevant academic research and scientific papers
Organocatalytic asymmetric conjugate addition of thioacetic acid to β-nitrostyrenes
Li, Hao,Wang, Jian,Zu, Liansuo,Wang, Wei
, p. 2585 - 2589 (2006)
A method for organocatalytic, enantioselective Michael addition reactions of thioacetic acid with a range of trans-β-nitrostyrenes has been developed. The processes, promoted by the chiral amine thiourea organocatalyst, take place in high yields with up t
Enantio- and diastereoselective addition of thioacetic acid to nitroalkenes via N-sulfinyl urea catalysis
Kimmel, Kyle L.,Robak, Maryann T.,Thomas, Stephen,Lee, Melissa,Ellman, Jonathan A.
experimental part, p. 2704 - 2712 (2012/04/17)
The enantioselective addition of thioacetic acid to nitroalkenes was achieved using N-sulfinyl urea catalysis. In this report, the scope of the reaction was extended to the enantio- and diastereoselective thioacetic acid addition to cyclic α,β-disubstitut
Enantioselective addition of thioacetic acid to nitroalkenes via N-sulfinyl urea organocatalysis
Kimmel, Kyle L.,Robak, MaryAnn T.,Ellman, Jonathan A.
supporting information; scheme or table, p. 8754 - 8755 (2009/12/04)
(Chemical Equation Presented) The highly enantioselective addition of thioacetic acid to nitroalkenes using a new sulfinyl urea organocatalyst is described. The addition of thioacetic acid proceeds in high yields and enantioselectivities for a variety of
