181492-01-3Relevant academic research and scientific papers
Bioreduction of β-carboline imines to amines employing Saccharomyces bayanus
Espinoza-Moraga, Marlene,Petta, Tania,Vasquez-Vasquez, Marco,Laurie, V. Felipe,Moraes, Luis A.B.,Santos, Leonardo Silva
, p. 1988 - 1992 (2010)
β-Carboline imine reductions mediated by Saccharomyces bayanus have been described achieving moderate to good enantiomeric excesses of the amine products. The enantiomeric excesses of the bioreduction showed a dependence on the imine substituents. Compoun
Catalytic asymmetric Pictet-Spengler reactions via sulfenyliminium ions
Wanner, Martin J.,Van Der Haas, Richard N. S.,De Cuba, Kimberly R.,Van Maarseveen, Jan H.,Hiemstra, Henk
, p. 7485 - 7487 (2008/09/17)
(Chemical Equation Presented) From cations to chiral products: β-Carbo-lines can be synthesized with good enantioselectivity by the title reaction catalyzed by a chiral binol-derived Bronsted acid (see scheme, BHT = 3,5-di(tert-butyl)-4-hydroxytoluene). T
