1,2-Diaza-1,3-dienes bearing electron-withdrawing groups react with electron-poor alkenes by means of an uncommon aza- Diels-Alder reaction furnishing novel tetrahydropyridazines with high regio- and stereoselectivity. Conducting these cycloadditions in solvent free conditions under thermal conditions the reaction times are significantly reduced, the yields are improved and the stereoselectivity remained unchanged
Catalyst-dependent [4 + 2]-cycloaddition reactions of azoalkenes from α-halohydrazones with enol dia...
A convenient, scalable synthesis of 1,2-dihydropyridazines is presented, based on the Diels-Alder cy...
A catalyst-free [4 + 2] annulation process between <i>in situ</i> generated 1,2-diaza-1,3-butadienes...
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...
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 synthesis of new 3-tetrazolyl-1,4,5,6-tetrahydropyridazines by Diels–Alder reactions of ethyl 3...
The inverse-electron-demand variant of the Diels-Alder reaction has been attracting strongly increas...
Abstract- The pyridazino[4,5-b]indole (3), which is conveniently available from 3-methylthioindole a...
A novel, facile, and efficient method for the synthesis of tetrahydropyridazines by a one-pot tandem...
The multicomponent 1,3-dipolar cycloaddition of different 1,2-diaza-1,3-dienes with in situ-generate...
The multicomponent 1,3-dipolar cycloaddition of different 1,2-diaza-1,3-dienes with in-situ-generate...
Catalytic inverse electron demand Diels Alder (IEDDA) reactions of heterocyclic aza-dienes are rarel...
Despite the poor reputation of electron-deficient pyridazines in intermolecular Hetero Diels-Alder (...
Catalyst-dependent [4 + 2]-cycloaddition reactions of azoalkenes from α-halohydrazones with enol dia...
A convenient, scalable synthesis of 1,2-dihydropyridazines is presented, based on the Diels-Alder cy...
A catalyst-free [4 + 2] annulation process between <i>in situ</i> generated 1,2-diaza-1,3-butadienes...
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...
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 synthesis of new 3-tetrazolyl-1,4,5,6-tetrahydropyridazines by Diels–Alder reactions of ethyl 3...
The inverse-electron-demand variant of the Diels-Alder reaction has been attracting strongly increas...
Abstract- The pyridazino[4,5-b]indole (3), which is conveniently available from 3-methylthioindole a...
A novel, facile, and efficient method for the synthesis of tetrahydropyridazines by a one-pot tandem...
The multicomponent 1,3-dipolar cycloaddition of different 1,2-diaza-1,3-dienes with in situ-generate...
The multicomponent 1,3-dipolar cycloaddition of different 1,2-diaza-1,3-dienes with in-situ-generate...
Catalytic inverse electron demand Diels Alder (IEDDA) reactions of heterocyclic aza-dienes are rarel...
Despite the poor reputation of electron-deficient pyridazines in intermolecular Hetero Diels-Alder (...
Catalyst-dependent [4 + 2]-cycloaddition reactions of azoalkenes from α-halohydrazones with enol dia...
A convenient, scalable synthesis of 1,2-dihydropyridazines is presented, based on the Diels-Alder cy...
A catalyst-free [4 + 2] annulation process between <i>in situ</i> generated 1,2-diaza-1,3-butadienes...