Premium
C 2 ‐Symmetric Cinchona Alkaloid Derivatives: Versatile Catalysts for the Enantioselective C−C Bond Forming Conjugate Addition of Nucleophiles to Simple α,β‐Unsaturated Acyl Pyrazoles
Author(s) -
Curran Simon P.,
Fallon Brendan J.,
Con Stephen J.
Publication year - 2020
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.202004505
Subject(s) - nucleophile , chemistry , enantioselective synthesis , cinchona , nitromethane , catalysis , organic chemistry , malononitrile , decarboxylation , michael reaction , allylic rearrangement , organocatalysis , combinatorial chemistry
A single C 2 ‐symmetric squaramide catalyst system allows the facile addition of either malononitrile or benzyl nitroacetate to simple pyrazole‐based Michael acceptors with excellent enantiocontrol and at lower catalyst loadings than previously possible. The latter reactions are not diastereoselective, however facile hydrogenolysis leads to decarboxylation and formation of the formal adduct from the addition of nitromethane (a very recalcitrant nucleophile in this chemistry) with excellent yield and enantiocontrol.