Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa, Japan.
Chem Commun (Camb). 2012 May 21;48(41):4986-8. doi: 10.1039/c2cc31530k. Epub 2012 Apr 16.
A highly effective catalytic enantioselective direct aminal synthesis was developed. Chiral ammonium 1,1'-binaphthyl-2,2'-disulfonates, which were prepared in situ from (R)-BINSA and achiral amines, promoted the enantioselective addition of primary amides to aromatic aldimines.
发展了一种高效的催化对映选择性直接胺化合成方法。手性铵 1,1'-联萘-2,2'-二磺酸盐,由 (R)-BINSA 和非手性胺原位制备,促进了伯酰胺与芳族亚胺的对映选择性加成。