A chiral Brønsted acid-catalyzed highly enantioselective Mannich-type reaction of α-diazo esters with in situ generated N-acyl ketimines.

Chem Commun (Camb)

Department of Chemistry, Indian Institute of Science Education and Research Bhopal, Bhopal, MP-462 066, India. and Department of Chemistry, Indian Institute of Technology Kanpur, Kanpur, UP-208016, India.

Published: April 2018

A chiral phosphoric acid-catalyzed asymmetric Mannich-type reaction of α-diazo esters with in situ generated N-acyl ketimines, derived from 3-hydroxyisoindolinones has been demonstrated in this communication. A variety of isoindolinone-based α-amino diazo esters bearing a quaternary stereogenic center were afforded in high yields (up to 99%) with excellent enantioselectivities (up to 99% ee). Furthermore, the synthetic utility of the products has been depicted by the hydrogenation of the diazo moiety of adducts.

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http://dx.doi.org/10.1039/C8CC01436ADOI Listing

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