A practical base-promoted tandem condensation N-alkylation reaction for the formation of trisubstituted hydrazones has been developed employing aldehydes and hydrazines with alkyl halides. Crucially, this reaction successfully overcomes chemoselectivity problems, allowing for the reaction of multiple components in a one-pot manner. Halo- and heterofunctional groups, as well as free hydroxyl and amino groups, are tolerated in this transformation to produce a wide range of trisubstituted hydrazones in good to excellent yields
A novel one-pot multicomponent synthesis of α-aminocarbonyl N-acylhydrazones starting from readily a...
A novel one-pot multicomponent synthesis of α-aminocarbonyl N-acylhydrazones starting from readily a...
A novel one-pot multicomponent synthesis of α-aminocarbonyl N-acylhydrazones starting from readily a...
A new, high-yielding methodology for reducing hydrazones to hydrazines is described, which allows th...
A one-pot procedure for the synthesis of hydrazines and hydrazides involves the redn. of hydrazones ...
Multicomponent reactions (MCR), as one-pot reactions, are effictient to synthesis target compounds w...
Multicomponent reactions (MCR), as one-pot reactions, are effictient to synthesis target compounds w...
N′-Alkyl hydrazides were effectively synthesized by routes featuring installation, alkylation, and r...
A ligand-free, palladium-catalyzed aminoarylation reaction of the unactivated alkenes in β,γ-unsatur...
A ligand-free, palladium-catalyzed aminoarylation reaction of the unactivated alkenes in β,γ-unsatur...
Isocyanide-based multicomponent reactions (IMCRs) allow the construction of relatively complex molec...
The intramolecular addition of hydrazone radicals to carbon–carbon double bonds was achieved by usin...
The intramolecular addition of hydrazone radicals to carbon–carbon double bonds was achieved by usin...
The intramolecular addition of hydrazone radicals to carbon–carbon double bonds was achieved by usin...
The intramolecular addition of hydrazone radicals to carbon–carbon double bonds was achieved by usin...
A novel one-pot multicomponent synthesis of α-aminocarbonyl N-acylhydrazones starting from readily a...
A novel one-pot multicomponent synthesis of α-aminocarbonyl N-acylhydrazones starting from readily a...
A novel one-pot multicomponent synthesis of α-aminocarbonyl N-acylhydrazones starting from readily a...
A new, high-yielding methodology for reducing hydrazones to hydrazines is described, which allows th...
A one-pot procedure for the synthesis of hydrazines and hydrazides involves the redn. of hydrazones ...
Multicomponent reactions (MCR), as one-pot reactions, are effictient to synthesis target compounds w...
Multicomponent reactions (MCR), as one-pot reactions, are effictient to synthesis target compounds w...
N′-Alkyl hydrazides were effectively synthesized by routes featuring installation, alkylation, and r...
A ligand-free, palladium-catalyzed aminoarylation reaction of the unactivated alkenes in β,γ-unsatur...
A ligand-free, palladium-catalyzed aminoarylation reaction of the unactivated alkenes in β,γ-unsatur...
Isocyanide-based multicomponent reactions (IMCRs) allow the construction of relatively complex molec...
The intramolecular addition of hydrazone radicals to carbon–carbon double bonds was achieved by usin...
The intramolecular addition of hydrazone radicals to carbon–carbon double bonds was achieved by usin...
The intramolecular addition of hydrazone radicals to carbon–carbon double bonds was achieved by usin...
The intramolecular addition of hydrazone radicals to carbon–carbon double bonds was achieved by usin...
A novel one-pot multicomponent synthesis of α-aminocarbonyl N-acylhydrazones starting from readily a...
A novel one-pot multicomponent synthesis of α-aminocarbonyl N-acylhydrazones starting from readily a...
A novel one-pot multicomponent synthesis of α-aminocarbonyl N-acylhydrazones starting from readily a...