We report a divergent and modular protocol for the preparation of acyclic molecular frameworks containing newly created quaternary carbon stereocenters. Central to this approach is a sequence composed of a (1) regioselective and -retentive preparation of allyloxycarbonyl-trapped fully substituted stereodefined amide enolates and of a (2) enantioselective palladium-catalyzed decarboxylative allylic alkylation reaction using a novel bisphosphine ligand
α-Quaternary ketones are accessed through novel enantioselective alkylations of allyl and propargyl ...
The development of a palladium-catalyzed enantioselective decarboxylative allylic alkylation of cycl...
A catalytic enantioselective method for the synthesis of α-quaternary Mannich-type products is repor...
We report a divergent and modular protocol for the preparation of acyclic molecular frameworks conta...
The first enantioselective palladium-catalyzed decarboxylative allylic alkylation of fully substitut...
The Pd-catalyzed decarboxylative asymmetric allylic alkylation of enolate nucleophiles is a cornerst...
Research in the Stoltz group is directed, generally, at the development of synthetic methods for the...
The palladium-catalyzed decarboxylative allylic alkylation of enol carbonates derived from lactams a...
A palladium-catalyzed decarboxylative asymmetric allylic alkylation (Pd-DAAA) of benzo-fused and non...
A palladium-catalyzed asymmetric decarboxylative allylic alkylation of allyl 2,2-diphenylglycinate i...
Stereochemical alchemy! Racemic allyl β-ketoesters allow the regiocontrolled formation of enolates, ...
As saturated heterocyclic building blocks become increasingly popular in medicinal chemistry and dru...
The enantioselective construction of a quaternary stereocenter in 2,3-dihydrofuran frameworks has be...
This account describes the circumstances leading to our group's innovations in the area of decarbox...
Enantioselective catalytic allylic alkylation for the synthesis of 2-alkyl-2-allylcycloalkanones and...
α-Quaternary ketones are accessed through novel enantioselective alkylations of allyl and propargyl ...
The development of a palladium-catalyzed enantioselective decarboxylative allylic alkylation of cycl...
A catalytic enantioselective method for the synthesis of α-quaternary Mannich-type products is repor...
We report a divergent and modular protocol for the preparation of acyclic molecular frameworks conta...
The first enantioselective palladium-catalyzed decarboxylative allylic alkylation of fully substitut...
The Pd-catalyzed decarboxylative asymmetric allylic alkylation of enolate nucleophiles is a cornerst...
Research in the Stoltz group is directed, generally, at the development of synthetic methods for the...
The palladium-catalyzed decarboxylative allylic alkylation of enol carbonates derived from lactams a...
A palladium-catalyzed decarboxylative asymmetric allylic alkylation (Pd-DAAA) of benzo-fused and non...
A palladium-catalyzed asymmetric decarboxylative allylic alkylation of allyl 2,2-diphenylglycinate i...
Stereochemical alchemy! Racemic allyl β-ketoesters allow the regiocontrolled formation of enolates, ...
As saturated heterocyclic building blocks become increasingly popular in medicinal chemistry and dru...
The enantioselective construction of a quaternary stereocenter in 2,3-dihydrofuran frameworks has be...
This account describes the circumstances leading to our group's innovations in the area of decarbox...
Enantioselective catalytic allylic alkylation for the synthesis of 2-alkyl-2-allylcycloalkanones and...
α-Quaternary ketones are accessed through novel enantioselective alkylations of allyl and propargyl ...
The development of a palladium-catalyzed enantioselective decarboxylative allylic alkylation of cycl...
A catalytic enantioselective method for the synthesis of α-quaternary Mannich-type products is repor...