TY - JOUR
T1 - Catalytic generation of α-CF3 enolate
T2 - Direct catalytic asymmetric Mannich-type reaction of α-CF3 amide
AU - Yin, Liang
AU - Brewitz, Lennart
AU - Kumagai, Naoya
AU - Shibasaki, Masakatsu
N1 - Publisher Copyright:
© 2014 American Chemical Society.
PY - 2014/12/31
Y1 - 2014/12/31
N2 - The introduction of the CF3 unit is a common strategy for modifying pharmacokinetic properties and slowing metabolic degradation in medicinal chemistry. A catalytic and enantioselective addition of α-CF3 enolates allows for expeditious access to functionalized chiral building blocks with CF3-containing stereogenicity. To date, α-CF3 enolates have been a less explored class of nucleophiles because of rapid defluorination. The present study reveals that a designed α-CF3 amide enables a direct asymmetric Mannich-type reaction in a cooperative catalytic system.
AB - The introduction of the CF3 unit is a common strategy for modifying pharmacokinetic properties and slowing metabolic degradation in medicinal chemistry. A catalytic and enantioselective addition of α-CF3 enolates allows for expeditious access to functionalized chiral building blocks with CF3-containing stereogenicity. To date, α-CF3 enolates have been a less explored class of nucleophiles because of rapid defluorination. The present study reveals that a designed α-CF3 amide enables a direct asymmetric Mannich-type reaction in a cooperative catalytic system.
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U2 - 10.1021/ja511458k
DO - 10.1021/ja511458k
M3 - Article
C2 - 25495289
AN - SCOPUS:84920170716
SN - 0002-7863
VL - 136
SP - 17958
EP - 17961
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 52
ER -