A new simple approach to the synthesis of unsymmetrical ureas HetNC(O)NRR¢ (HetNH = pyrrole, indole, carbazole; R, R¢ = H, alkyl, aryl) has been explored, which involves the direct reaction of the N-phenoxycarbonyl derivatives of pyrrole, indole and carbazole, HetNCO2Ph, with amines. The aminolysis reaction can be catalyzed by the amidine base DBU (1,8-diazabicyclo[5.4.0]undec-7-ene) under usually very mild conditions and provides a straightforward convenient entry into the target products through a route which avoids the traditional protocols based on multistep procedures and toxic phosgene or phosgene-derivatives
Abstract. In this thesis the synthesis of potentially biologically active heterocyclic compounds has...
We gratefully acknowledge financial support from the BBSRC (Grant no. BB/I022910/1 and the European ...
<p>An efficient method for the synthesis of urea and carbamate derivatives from amines and alcohols ...
A convenient method toward the synthesis of α-amino acid-derived unsymmetrical ureas 2 is described ...
A convenient method toward the synthesis of alpha-amino acid-derived unsymmetrical ureas 2 is descri...
Selective hydrolysis of carbonimidodithioates (3) leads to the thiocarbamates (4), which can be easi...
A simple and efficient two-step synthesis of unsymmetrically substituted ureas containing an amino a...
Synthesizing nitrogen containing heterocyclic compounds is one of the leading research areas through...
International audienceA direct and convenient method for the preparation of N-substituted ureas is a...
N-Heteroaromatics HetNH, such as pyrrole (1), indole (2) and carbazole (3), have been selectively N...
Ureas are a very important class of carbonyl compounds which find extensive application as agrochemi...
AbstractA simple and efficient route for the synthesis of Unsymmetrical N,N′-diphenyl urea have been...
An efficient parallel synthesis of ureas based on amino acids is described, both in solution and on ...
In the search for new drug compounds, the current focus has been shifted to a class of compounds cal...
In a simple, one-pot procedure, H<sub>2</sub>O<sub>2</sub> has been utilised for the synthesis of un...
Abstract. In this thesis the synthesis of potentially biologically active heterocyclic compounds has...
We gratefully acknowledge financial support from the BBSRC (Grant no. BB/I022910/1 and the European ...
<p>An efficient method for the synthesis of urea and carbamate derivatives from amines and alcohols ...
A convenient method toward the synthesis of α-amino acid-derived unsymmetrical ureas 2 is described ...
A convenient method toward the synthesis of alpha-amino acid-derived unsymmetrical ureas 2 is descri...
Selective hydrolysis of carbonimidodithioates (3) leads to the thiocarbamates (4), which can be easi...
A simple and efficient two-step synthesis of unsymmetrically substituted ureas containing an amino a...
Synthesizing nitrogen containing heterocyclic compounds is one of the leading research areas through...
International audienceA direct and convenient method for the preparation of N-substituted ureas is a...
N-Heteroaromatics HetNH, such as pyrrole (1), indole (2) and carbazole (3), have been selectively N...
Ureas are a very important class of carbonyl compounds which find extensive application as agrochemi...
AbstractA simple and efficient route for the synthesis of Unsymmetrical N,N′-diphenyl urea have been...
An efficient parallel synthesis of ureas based on amino acids is described, both in solution and on ...
In the search for new drug compounds, the current focus has been shifted to a class of compounds cal...
In a simple, one-pot procedure, H<sub>2</sub>O<sub>2</sub> has been utilised for the synthesis of un...
Abstract. In this thesis the synthesis of potentially biologically active heterocyclic compounds has...
We gratefully acknowledge financial support from the BBSRC (Grant no. BB/I022910/1 and the European ...
<p>An efficient method for the synthesis of urea and carbamate derivatives from amines and alcohols ...