We report a highly enantioselective, general catalytic system for the facile synthesis of tertiary stereocenters by protonation adjacent to cyclic ketones. The method relies on catalytic decarboxylative protonation of readily accessible racemic quaternary β-ketoesters. A range of substituted cycloalkanone compounds can be accessed through this process with high levels of enantioselectivity
General catalytic asymmetric routes toward cyclopentanoid and cycloheptanoid core structures embedde...
The first general method for the enantioselective construction of all-carbon quaternary centers on c...
Mechanism and the origin of enantioselectivity in the decarboxylative protonation of α-amino malonat...
We report a highly enantioselective, general catalytic system for the facile synthesis of tertiary s...
General homogeneous conditions for the palladium-catalyzed synthesis of carbonyl compounds with tert...
Enantioselective protonation is a common process in biosynthetic sequences. The decarboxylase and es...
Herein, we describe a study into the scope and origin of an enantiodivergent effect in the palladium...
We report a highly enantioselective catalytic protonation of bis‐silyl ketene acetals. Our method de...
α-Quaternary ketones are accessed through novel enantioselective alkylations of allyl and propargyl ...
International audienceThe palladium‐catalyzed decarboxylative asymmetric protonation (DAP) of racemi...
The direct α-vinylation of carbonyl compounds to form a quaternary stereocenter is a challenging tra...
The catalytic enantioselective preparation of all-carbon quaternary stereocenters within rings via a...
The use of high-throughput screening allowed for the optimization of reaction conditions for the pal...
The palladium-catalyzed decarboxylative allylic alkylation of enol carbonates derived from lactams a...
An enantioselective synthesis of diverse N4-Boc-protected α,α-disubstituted piperazin-2-ones using t...
General catalytic asymmetric routes toward cyclopentanoid and cycloheptanoid core structures embedde...
The first general method for the enantioselective construction of all-carbon quaternary centers on c...
Mechanism and the origin of enantioselectivity in the decarboxylative protonation of α-amino malonat...
We report a highly enantioselective, general catalytic system for the facile synthesis of tertiary s...
General homogeneous conditions for the palladium-catalyzed synthesis of carbonyl compounds with tert...
Enantioselective protonation is a common process in biosynthetic sequences. The decarboxylase and es...
Herein, we describe a study into the scope and origin of an enantiodivergent effect in the palladium...
We report a highly enantioselective catalytic protonation of bis‐silyl ketene acetals. Our method de...
α-Quaternary ketones are accessed through novel enantioselective alkylations of allyl and propargyl ...
International audienceThe palladium‐catalyzed decarboxylative asymmetric protonation (DAP) of racemi...
The direct α-vinylation of carbonyl compounds to form a quaternary stereocenter is a challenging tra...
The catalytic enantioselective preparation of all-carbon quaternary stereocenters within rings via a...
The use of high-throughput screening allowed for the optimization of reaction conditions for the pal...
The palladium-catalyzed decarboxylative allylic alkylation of enol carbonates derived from lactams a...
An enantioselective synthesis of diverse N4-Boc-protected α,α-disubstituted piperazin-2-ones using t...
General catalytic asymmetric routes toward cyclopentanoid and cycloheptanoid core structures embedde...
The first general method for the enantioselective construction of all-carbon quaternary centers on c...
Mechanism and the origin of enantioselectivity in the decarboxylative protonation of α-amino malonat...