posted on 2020-08-19, 21:05authored byShweta
K. Gediya, Guy J. Clarkson, Martin Wills
A series of α-amino
ketones were reduced using asymmetric
transfer hydrogenation (ATH) through a dynamic kinetic resolution
(DKR). The protecting group was matched to the reducing agent, and
following optimization, a series of substrates were investigated,
giving products in high diastereoselectivity, over 99% ee in several
cases and full conversion. The methodology was applied to the enantioselective
synthesis of an MDM2–p53 inhibitor precursor.