Janey Jacob M
Department of Process Research, Merck Research Laboratories, Merck & Co., Inc. P.O. Box 2000, Rahway, NJ 07065, USA.
Angew Chem Int Ed Engl. 2005 Jul 11;44(28):4292-300. doi: 10.1002/anie.200462314.
The direct introduction of either a nitrogen or oxygen atom adjacent to a carbonyl group in a catalytic, enantioselective manner using both chiral Lewis acid and Lewis base catalysis has been described recently. The enantiomerically enriched products of these reactions, such as alpha-amino acids, represent fundamental building blocks for the construction of complex natural products and other important bioactive molecules. This Minireview provides a synopsis of this ever-growing field and highlights some of the challenges that still remain.
最近已有报道,利用手性路易斯酸和路易斯碱催化,以催化对映选择性方式在羰基相邻位置直接引入氮原子或氧原子。这些反应的对映体富集产物,如α-氨基酸,是构建复杂天然产物和其他重要生物活性分子的基本构件。本综述概述了这一不断发展的领域,并强调了一些仍然存在的挑战。