Asymmetric Catalytic Ketimine Mannich Reactions and Related Transformations.

Catalysts

Chemistry Program, Department of Biomedical and Chemical Engineering and Sciences, Florida Institute of Technology, 150 West University Boulevard, Melbourne, FL 32901-6975, USA.

Published: June 2021

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8570560PMC
http://dx.doi.org/10.3390/catal11060712DOI Listing

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