We present a redox-neutral method for the photocatalytic generation of carbanions. Benzylic carboxylates are photooxidized by single electron transfer; immediate CO2 extrusion and reduction of the in situ formed radical yields a carbanion capable of reacting with aliphatic aldehydes as electrophiles giving the Grignard analogous reaction product. </bold
The combination of photoredox catalysis with the Wolff−Kishner (WK) reaction allows the difunctional...
The development of green and sustainable methods for the conversion of aldehydes to carboxylic acids...
Aminodecarboxylation of unactivated alkyl carboxylic acids has been accomplished utilizing an organi...
We present a redox-neutral method for the photocatalytic generation of carbanions. Benzylic carboxyl...
We present a redox-neutral method for the photocatalytic generation of carbanions. Benzylic carboxy...
We report a redox-neutral method for the generation of carbanions from benzylic C-H bonds in a photo...
We report a redox‐neutral method for the generation of carbanions from benzylic C–H bonds in a photo...
Organometallic reagents are routinely used as fundamental building blocks in organic chemistry to ra...
The use of photocatalysis in organic chemistry has encountered a surge of novel transformations sinc...
The carboxylation of sp(3)-hybridized C-H bonds with CO2 is a challenging transformation. Herein, we...
A metal-free generation of carbanion nucleophiles is of prime importance in organic synthesis. Herei...
A metal-free generation of carbanion nucleophiles is of prime importance in organic synthesis. Herei...
An efficient and environmentally benign method for the oxidation of aldehydes to carboxylic acids ha...
Arylacetic acids were used as sources of benzyl radicals under tetrabutylammonium decatungstate phot...
The direct conversion of aliphatic carboxylic acids to the corresponding alkyl fluorides has been ac...
The combination of photoredox catalysis with the Wolff−Kishner (WK) reaction allows the difunctional...
The development of green and sustainable methods for the conversion of aldehydes to carboxylic acids...
Aminodecarboxylation of unactivated alkyl carboxylic acids has been accomplished utilizing an organi...
We present a redox-neutral method for the photocatalytic generation of carbanions. Benzylic carboxyl...
We present a redox-neutral method for the photocatalytic generation of carbanions. Benzylic carboxy...
We report a redox-neutral method for the generation of carbanions from benzylic C-H bonds in a photo...
We report a redox‐neutral method for the generation of carbanions from benzylic C–H bonds in a photo...
Organometallic reagents are routinely used as fundamental building blocks in organic chemistry to ra...
The use of photocatalysis in organic chemistry has encountered a surge of novel transformations sinc...
The carboxylation of sp(3)-hybridized C-H bonds with CO2 is a challenging transformation. Herein, we...
A metal-free generation of carbanion nucleophiles is of prime importance in organic synthesis. Herei...
A metal-free generation of carbanion nucleophiles is of prime importance in organic synthesis. Herei...
An efficient and environmentally benign method for the oxidation of aldehydes to carboxylic acids ha...
Arylacetic acids were used as sources of benzyl radicals under tetrabutylammonium decatungstate phot...
The direct conversion of aliphatic carboxylic acids to the corresponding alkyl fluorides has been ac...
The combination of photoredox catalysis with the Wolff−Kishner (WK) reaction allows the difunctional...
The development of green and sustainable methods for the conversion of aldehydes to carboxylic acids...
Aminodecarboxylation of unactivated alkyl carboxylic acids has been accomplished utilizing an organi...