The direct mechanochemical amidation of esters by ball milling is described. The operationally simple procedure requires an ester, an amine, and substoichiometric KOtBu and was used to prepare a large and diverse library of 78 amide structures with modest to excellent efficiency. Heteroaromatic and heterocyclic components are specifically shown to be amenable to this mechanochemical protocol. This direct synthesis platform has been applied to the synthesis of active pharmaceutical ingredients (APIs) and agrochemicals as well as the gram-scale synthesis of an active pharmaceutical, all in the absence of a reaction solvent
Discovered over a century ago, Beckmann rearrangement is still today fully compliant with all the gr...
A catalytic amidation protocol mediated by 2,2,2-trifluoroethanol has been developed, facilitating t...
Milling of cyanoacetamide and acetoacetic ester as reactants, in the presence of KOH as the catalyst...
The direct mechanochemical amidation of esters by ball milling is described. The operationally simpl...
The direct mechanochemical amidation of esters by ball milling is described. The operationally simpl...
A ball-milling enabled tertiary amine catalyzed aza-Morita–Baylis–Hillman reaction is reported. The ...
A ball-milling enabled tertiary amine catalyzed aza-Morita–Baylis–Hillman reaction is reported. The ...
Within this thesis is described a series of studies into performing organic synthesis under mechanoc...
Two robust and efficient mechanochemical protocols for the synthesis of an array of N-arylamides hav...
Two easily accessible routes for preparing an array of formylated and acetylated amines under mechan...
A catalytic protocol for the base-mediated amidation of unactivated esters with amino alcohol deriva...
We describe the development of a sustainable ester amidation process. Base and solvent screening, co...
A catalytic amidation method has been developed, employing 2,2,2-trifluoroethanol to facilitate cond...
A catalytic amidation method has been developed, employing 2,2,2-trifluoroethanol to facilitate cond...
Discovered over a century ago, Beckmann rearrangement is still today fully compliant with all the gr...
Discovered over a century ago, Beckmann rearrangement is still today fully compliant with all the gr...
A catalytic amidation protocol mediated by 2,2,2-trifluoroethanol has been developed, facilitating t...
Milling of cyanoacetamide and acetoacetic ester as reactants, in the presence of KOH as the catalyst...
The direct mechanochemical amidation of esters by ball milling is described. The operationally simpl...
The direct mechanochemical amidation of esters by ball milling is described. The operationally simpl...
A ball-milling enabled tertiary amine catalyzed aza-Morita–Baylis–Hillman reaction is reported. The ...
A ball-milling enabled tertiary amine catalyzed aza-Morita–Baylis–Hillman reaction is reported. The ...
Within this thesis is described a series of studies into performing organic synthesis under mechanoc...
Two robust and efficient mechanochemical protocols for the synthesis of an array of N-arylamides hav...
Two easily accessible routes for preparing an array of formylated and acetylated amines under mechan...
A catalytic protocol for the base-mediated amidation of unactivated esters with amino alcohol deriva...
We describe the development of a sustainable ester amidation process. Base and solvent screening, co...
A catalytic amidation method has been developed, employing 2,2,2-trifluoroethanol to facilitate cond...
A catalytic amidation method has been developed, employing 2,2,2-trifluoroethanol to facilitate cond...
Discovered over a century ago, Beckmann rearrangement is still today fully compliant with all the gr...
Discovered over a century ago, Beckmann rearrangement is still today fully compliant with all the gr...
A catalytic amidation protocol mediated by 2,2,2-trifluoroethanol has been developed, facilitating t...
Milling of cyanoacetamide and acetoacetic ester as reactants, in the presence of KOH as the catalyst...