Development of Catalytic Enantioselective Mannich Reactions Using Esters.

Org Lett

Department of Chemistry, School of Science, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo Japan, 113-0033.

Published: March 2024

Catalytic enantioselective Mannich reactions of simple nonactivated esters proceeded using a chiral potassium strong base catalyst prepared from a chiral bisoxazoline and potassium hexamethyldisilazide. Alkyl acetates, alkyl propionates, and an alkyl butyrate were employed as the simple esters, and the desired reactions proceeded smoothly to afford Mannich products in good to high yields with high enantioselectivities. One of the products was successfully employed in the asymmetric total synthesis of Maraviroc.

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http://dx.doi.org/10.1021/acs.orglett.3c04326DOI Listing

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