Add to ORKGAlkyl oxalates are new bench-stable alcohol-activating groups for radical generation under visible light photoredox conditions. Using these precursors, the first net redox-neutral coupling of tertiary and secondary alcohols with electron-deficient alkenes is achieved
Despite many recent advances in the radical alkylation of electron-deficient heteroarenes since the ...
In Chapter 1, alkyl oxalates are described as new bench-stable alcohol activating groups for radical...
A convenient method for the direct construction of quaternary carbons from tertiary alcohols by visi...
Alkyl oxalates are new bench-stable alcohol-activating groups for radical generation under visible l...
Alkyl oxalates are new bench-stable alcohol-activating groups for radical generation under visible l...
Alkyl oxalates are new bench-stable alcohol-activating groups for radical generation under visible l...
The coupling of tertiary carbon radicals with alkene acceptors is an underdeveloped strategy for uni...
The coupling of tertiary carbon radicals with alkene acceptors is an underdeveloped strategy for uni...
The coupling of tertiary carbon radicals with alkene acceptors is an underdeveloped strategy for uni...
A convenient method for the direct construction of quaternary carbons from tertiary alcohols by visi...
The coupling of tertiary carbon radicals with alkene acceptors is an underdeveloped strategy for uni...
The coupling of tertiary carbon radicals with alkene acceptors is an underdeveloped strategy for uni...
The coupling of tertiary carbon radicals with alkene acceptors is an underdeveloped strategy for uni...
Despite many recent advances in the radical alkylation of electron-deficient heteroarenes since the ...
Despite many recent advances in the radical alkylation of electron-deficient heteroarenes since the ...
Despite many recent advances in the radical alkylation of electron-deficient heteroarenes since the ...
In Chapter 1, alkyl oxalates are described as new bench-stable alcohol activating groups for radical...
A convenient method for the direct construction of quaternary carbons from tertiary alcohols by visi...
Alkyl oxalates are new bench-stable alcohol-activating groups for radical generation under visible l...
Alkyl oxalates are new bench-stable alcohol-activating groups for radical generation under visible l...
Alkyl oxalates are new bench-stable alcohol-activating groups for radical generation under visible l...
The coupling of tertiary carbon radicals with alkene acceptors is an underdeveloped strategy for uni...
The coupling of tertiary carbon radicals with alkene acceptors is an underdeveloped strategy for uni...
The coupling of tertiary carbon radicals with alkene acceptors is an underdeveloped strategy for uni...
A convenient method for the direct construction of quaternary carbons from tertiary alcohols by visi...
The coupling of tertiary carbon radicals with alkene acceptors is an underdeveloped strategy for uni...
The coupling of tertiary carbon radicals with alkene acceptors is an underdeveloped strategy for uni...
The coupling of tertiary carbon radicals with alkene acceptors is an underdeveloped strategy for uni...
Despite many recent advances in the radical alkylation of electron-deficient heteroarenes since the ...
Despite many recent advances in the radical alkylation of electron-deficient heteroarenes since the ...
Despite many recent advances in the radical alkylation of electron-deficient heteroarenes since the ...
In Chapter 1, alkyl oxalates are described as new bench-stable alcohol activating groups for radical...
A convenient method for the direct construction of quaternary carbons from tertiary alcohols by visi...