Abstract
A new general de
novo synthesis of pharmaceutically important N-(hetero)aryl piperidines is reported. This protocol uses a
robustly diastereoselective reductive amination/aza-Michael reaction sequence to
achieve rapid construction of complex polysubstituted ring systems starting
from widely available heterocyclic amine nucleophiles and carbonyl
electrophiles. Notably, the diastereoselectivity of this process is enhanced by
the presence of water, and DFT calculations support a stereochemical model
involving a facially selective protonation of a water-coordinated enol
intermediate.
Supplementary materials
Title
PIP SI FINAL
Description
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Title
PIP SI FINAL
Description
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Title
Piperidine SATHER FINAL
Description
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