Xu Changgong, Reep Carlyn, Jarvis Jamielyn, Naumann Brandon, Captain Burjor, Takenaka Norito
Chemistry Program, Department of Biomedical and Chemical Engineering and Sciences, Florida Institute of Technology, 150 West University Boulevard, Melbourne, FL 32901-6975, USA.
Department of Chemistry, University of Miami, 1301 Memorial Drive, Coral Gables, FL 33146-0431, USA.
Catalysts. 2021 Jun;11(6). doi: 10.3390/catal11060712. Epub 2021 Jun 7.
The catalytic enantioselective ketimine Mannich and its related reactions provide direct access to chiral building blocks bearing an α-tertiary amine stereogenic center, a ubiquitous structural motif in nature. Although ketimines are often viewed as challenging electrophiles, various approaches/strategies to circumvent or overcome the adverse properties of ketimines have been developed for these transformations. This review showcases the selected examples that highlight the benefits and utilities of various ketimines and remaining challenges associated with them in the context of Mannich, allylation, and aza-Morita-Baylis-Hillman reactions as well as their variants.
催化对映选择性酮亚胺曼尼希反应及其相关反应可直接得到带有α-叔胺立体中心的手性结构单元,这是自然界中普遍存在的结构基序。尽管酮亚胺通常被视为具有挑战性的亲电试剂,但已开发出各种方法/策略来规避或克服酮亚胺的不利性质以用于这些转化反应。本综述展示了一些精选实例,这些实例突出了各种酮亚胺在曼尼希反应、烯丙基化反应、氮杂-森田-贝利斯-希尔曼反应及其变体反应中的优势和用途,以及与之相关的尚存挑战。