Nitroalkanes activated with polyphosphoric acid serve as efficient electrophiles in reactions with various nucleophilic amines. Strategically placed second functionality allows for the design of annulation reactions enabling preparation of various heterocycles. This strategy was employed to develop an innovative synthetic approach towards 3,4-dihydroquinazolines from readily available 2-(aminomethyl)anilines
A new series of 3,4-disubstituted quinazolin-2-ones, with potential T-type calcium channel antagonis...
The 1,2,3,4-tetrahydroisoquinoline derived push-pull enaminones and nitroenamine have been investiga...
An efficient route to <i>N</i><sup>4</sup>-substituted 2,4-diaminoquinazolines has been developed by...
Nitroalkanes activated with polyphosphoric acid serve as efficient electrophiles in reactions with v...
Nitroalkanes activated with polyphosphoric acid serve as efficient electrophiles in reactions with v...
Nitroalkanes activated with polyphosphoric acid could serve as efficient electrophiles in reactions ...
Nitroalkanes activated with polyphosphoric acid could serve as efficient electrophiles in reactions ...
The sequential N-functionalization of 2-aminobenzylamine (2-ABA) followed by cyclodehydration allowe...
A straightforward strategy for the synthesis of dihydroquinazolines is presented, which allows for t...
The sequential N-functionalization of 2-aminobenzylamine (2-ABA) followed by cyclodehydration allowe...
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.A...
This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. Ma...
A new method for the synthesis of 6,7-dimethoxy-3,4-dihydroisoquinoline based on the reaction of 2-(...
A highly efficient and simple one-pot reaction for the synthesis of three-component assembly of dive...
Herein we disclose a mild protocol for the reductive functionalisation of quinolinium and isoquinoli...
A new series of 3,4-disubstituted quinazolin-2-ones, with potential T-type calcium channel antagonis...
The 1,2,3,4-tetrahydroisoquinoline derived push-pull enaminones and nitroenamine have been investiga...
An efficient route to <i>N</i><sup>4</sup>-substituted 2,4-diaminoquinazolines has been developed by...
Nitroalkanes activated with polyphosphoric acid serve as efficient electrophiles in reactions with v...
Nitroalkanes activated with polyphosphoric acid serve as efficient electrophiles in reactions with v...
Nitroalkanes activated with polyphosphoric acid could serve as efficient electrophiles in reactions ...
Nitroalkanes activated with polyphosphoric acid could serve as efficient electrophiles in reactions ...
The sequential N-functionalization of 2-aminobenzylamine (2-ABA) followed by cyclodehydration allowe...
A straightforward strategy for the synthesis of dihydroquinazolines is presented, which allows for t...
The sequential N-functionalization of 2-aminobenzylamine (2-ABA) followed by cyclodehydration allowe...
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.A...
This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. Ma...
A new method for the synthesis of 6,7-dimethoxy-3,4-dihydroisoquinoline based on the reaction of 2-(...
A highly efficient and simple one-pot reaction for the synthesis of three-component assembly of dive...
Herein we disclose a mild protocol for the reductive functionalisation of quinolinium and isoquinoli...
A new series of 3,4-disubstituted quinazolin-2-ones, with potential T-type calcium channel antagonis...
The 1,2,3,4-tetrahydroisoquinoline derived push-pull enaminones and nitroenamine have been investiga...
An efficient route to <i>N</i><sup>4</sup>-substituted 2,4-diaminoquinazolines has been developed by...