α,β-Unsaturated esters are readily available but challenging substrates to activate in asymmetric catalysis. We now describe an efficient, general, and highly enantioselective Mukaiyama–Michael reaction of silyl ketene acetals with α,β-unsaturated methyl esters that is catalyzed by a silylium imidodiphosphorimidate (IDPi) Lewis acid
The l-menthone-derived TADDOL phosphite 6b catalyzes highly enantioselective conjugate additions of ...
418 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2008.A catalytic system involving ...
Nitronate anions, formally generated by α-deprotonating the corresponding nitroalkanes, are highly n...
Despite tremendous advances in enantioselective catalysis of the Diels−Alder reaction, the use of si...
The fundamental substrate class of α,β-unsaturated esters offers extraordinary synthetic potential f...
The fundamental substrate class of α,β-unsaturated esters offers extraordinary synthetic po...
The chemical synthesis of organic molecules involves, at its very essence, the creation of carbon–ca...
LUMO-lowering organocatalysis has been extended to promote the conjugate addition of S-alkyl and 1-p...
LUMO-lowering organocatalysis has been extended to promote the conjugate addition of S-alkyl and 1-p...
Touched for the very first time! It is herein highlighted how acetaldehyde silyl enol ethers undergo...
Reactions that form a product with the same reactive functionality as that of one of the starting co...
MB thanks EaStCHEM and the School of Chemistry for support.An enantioselective Michael addition of m...
A highly enantioselective organocatalytic Mukaiyama-Michael reaction of silyloxy dienes and α,β-unsa...
High acidity and structural confinement are pivotal elements in asymmetric acid catalysis. The recen...
The l-menthone-derived TADDOL phosphite 6b catalyzes highly enantioselective conjugate additions of ...
The l-menthone-derived TADDOL phosphite 6b catalyzes highly enantioselective conjugate additions of ...
418 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2008.A catalytic system involving ...
Nitronate anions, formally generated by α-deprotonating the corresponding nitroalkanes, are highly n...
Despite tremendous advances in enantioselective catalysis of the Diels−Alder reaction, the use of si...
The fundamental substrate class of α,β-unsaturated esters offers extraordinary synthetic potential f...
The fundamental substrate class of α,β-unsaturated esters offers extraordinary synthetic po...
The chemical synthesis of organic molecules involves, at its very essence, the creation of carbon–ca...
LUMO-lowering organocatalysis has been extended to promote the conjugate addition of S-alkyl and 1-p...
LUMO-lowering organocatalysis has been extended to promote the conjugate addition of S-alkyl and 1-p...
Touched for the very first time! It is herein highlighted how acetaldehyde silyl enol ethers undergo...
Reactions that form a product with the same reactive functionality as that of one of the starting co...
MB thanks EaStCHEM and the School of Chemistry for support.An enantioselective Michael addition of m...
A highly enantioselective organocatalytic Mukaiyama-Michael reaction of silyloxy dienes and α,β-unsa...
High acidity and structural confinement are pivotal elements in asymmetric acid catalysis. The recen...
The l-menthone-derived TADDOL phosphite 6b catalyzes highly enantioselective conjugate additions of ...
The l-menthone-derived TADDOL phosphite 6b catalyzes highly enantioselective conjugate additions of ...
418 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2008.A catalytic system involving ...
Nitronate anions, formally generated by α-deprotonating the corresponding nitroalkanes, are highly n...