Trost Barry M, Weiss Andrew H
Department of Chemistry, Stanford University, Stanford, California 94305-5080.
Department of Chemistry & Chemical Biology, Harvard University, 12 Oxford St., Cambridge, MA 02138.
Adv Synth Catal. 2009 May;351(7-8). doi: 10.1002/adsc.200800776.
Over the past decade, large strides have been achieved in the invention of methods for the direct enantioselective addition of alkynes and metal alkynylide nucleophiles into prochiral aldehydes, ketones, and imines. This review highlights and compares the available methods for these transformations.
在过去十年中,在将炔烃和金属炔化物亲核试剂直接对映选择性加成到前手性醛、酮和亚胺的方法发明方面取得了长足进展。本综述重点介绍并比较了用于这些转化的现有方法。