A novel, facile, and efficient method for the synthesis of tetrahydropyridazines by a one-pot tandem reaction of easily accessible ketohydrazones and olefins in the presence of 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) has been successfully developed. The reaction involves the initial generation of azoalkenes from direct oxidative dehydrogenation of ketohydrazones using TEMPO as the commercially available oxidant, followed by a subsequent aza-Diels–Alder reaction with olefins
Total synthesis has evolved as a valuable tool for the development of novel synthetic compounds and ...
This thesis generalises the earlier reported one pot synthesis of 1,2,3,4-tetrahydroquinoline deriva...
A convenient, scalable synthesis of 1,2-dihydropyridazines is presented, based on the Diels-Alder cy...
A novel, facile, and efficient method for the synthesis of tetrahydropyridazines by a one-pot tandem...
The reaction of ketohydrazones containing an α-methylene group with chloramine-T followed by treatme...
1,2-Diaza-1,3-dienes bearing electron-withdrawing groups react with electron-poor alkenes by means o...
Cyclic ketohydrazones containing -methylene group are oxidized by chloramine-T followed by treatment...
1,2-Diaza-1,3-dienes bearing electron-withdrawing groups react with electron-poor alkenes by means o...
1,2-Diaza-1,3-dienes bearing electron withdrawing groups react with electron-poor alkenes by means o...
A highly efficient formal inverse electron demand aza Diels–Alder reaction of 1,2-diaza-1,3-dienes (...
The reaction of 3,6-diphenyl-1,2,4,5-tetrazine 1 with cis,cis-cycloocta-1,5-diene 7 has been studied...
Catalyst-dependent [4 + 2]-cycloaddition reactions of azoalkenes from α-halohydrazones with enol dia...
The intramolecular addition of hydrazone radicals to carbon–carbon double bonds was achieved by usin...
Metal-free, formal [2 + 2 + 2] cycloaddition st rategies for the synthesis of polycyclic pyridine de...
The Alpha, Beta unsaturated hydrazone reacts regioselectivity with a wide range of dienophiles to gi...
Total synthesis has evolved as a valuable tool for the development of novel synthetic compounds and ...
This thesis generalises the earlier reported one pot synthesis of 1,2,3,4-tetrahydroquinoline deriva...
A convenient, scalable synthesis of 1,2-dihydropyridazines is presented, based on the Diels-Alder cy...
A novel, facile, and efficient method for the synthesis of tetrahydropyridazines by a one-pot tandem...
The reaction of ketohydrazones containing an α-methylene group with chloramine-T followed by treatme...
1,2-Diaza-1,3-dienes bearing electron-withdrawing groups react with electron-poor alkenes by means o...
Cyclic ketohydrazones containing -methylene group are oxidized by chloramine-T followed by treatment...
1,2-Diaza-1,3-dienes bearing electron-withdrawing groups react with electron-poor alkenes by means o...
1,2-Diaza-1,3-dienes bearing electron withdrawing groups react with electron-poor alkenes by means o...
A highly efficient formal inverse electron demand aza Diels–Alder reaction of 1,2-diaza-1,3-dienes (...
The reaction of 3,6-diphenyl-1,2,4,5-tetrazine 1 with cis,cis-cycloocta-1,5-diene 7 has been studied...
Catalyst-dependent [4 + 2]-cycloaddition reactions of azoalkenes from α-halohydrazones with enol dia...
The intramolecular addition of hydrazone radicals to carbon–carbon double bonds was achieved by usin...
Metal-free, formal [2 + 2 + 2] cycloaddition st rategies for the synthesis of polycyclic pyridine de...
The Alpha, Beta unsaturated hydrazone reacts regioselectivity with a wide range of dienophiles to gi...
Total synthesis has evolved as a valuable tool for the development of novel synthetic compounds and ...
This thesis generalises the earlier reported one pot synthesis of 1,2,3,4-tetrahydroquinoline deriva...
A convenient, scalable synthesis of 1,2-dihydropyridazines is presented, based on the Diels-Alder cy...