Dipolar cycloadditions of azomethine imines, formed in situ from aldehydes and N1-alkyl-N2-acylhydrazines, with electron-deficient dipolarophiles produce pyrazolidines: mono-substituted dipolarophiles afford principally 4-substituted pyrazolidines
Centre of Advanced Studies on Natural Products including Organic Synthesis, Department of Chemistry,...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
—The regio- and diastereoselective synthesis of pyrrolidine derivatives through 1,3-dipolar cycloadd...
Dipolar cycloadditions of azomethine imines, formed in situ from aldehydes and N1-alkyl-N2- acylhydr...
A catalytic method involving carbenoid insertion onto dihydroimidazoles is reported for the generati...
1,3-Dipolar reactions of imines of both acyclic and cyclic α-amino esters with a range of nitroolefi...
A study of the reactivity of a non-stabilised azomethine ylide, derived from N-(methoxymethyl)-N-(tr...
2-Thio-3-chloroacrylamides undergo 1,3-dipolar cycloadditions with diazoalkanes leading to a series ...
Azomethine imines are considered 1,3-dipoles of the aza-allyl type which are transient intermediates...
A multicomponent 1,3-dipolar cycloaddition between heterocyclic aldehydes, amino esters and dipolaro...
1,3-Dipolar reactions of imines of both acyclic and cyclic α-amino esters with a range of nitroolefi...
Abstract: Nitrile imines generated by the oxidative dehydrogenation of aromatic aldehyde phenylhydra...
International audienceN-Metallated azomethine ylide generated from methyl (E)-N-benzylideneglycinate...
This review summarizes the trends in the formation of complex or not so complex heterocyclic structu...
textA novel application of the Pauson-Khand reaction was applied to the synthesis of a series of bri...
Centre of Advanced Studies on Natural Products including Organic Synthesis, Department of Chemistry,...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
—The regio- and diastereoselective synthesis of pyrrolidine derivatives through 1,3-dipolar cycloadd...
Dipolar cycloadditions of azomethine imines, formed in situ from aldehydes and N1-alkyl-N2- acylhydr...
A catalytic method involving carbenoid insertion onto dihydroimidazoles is reported for the generati...
1,3-Dipolar reactions of imines of both acyclic and cyclic α-amino esters with a range of nitroolefi...
A study of the reactivity of a non-stabilised azomethine ylide, derived from N-(methoxymethyl)-N-(tr...
2-Thio-3-chloroacrylamides undergo 1,3-dipolar cycloadditions with diazoalkanes leading to a series ...
Azomethine imines are considered 1,3-dipoles of the aza-allyl type which are transient intermediates...
A multicomponent 1,3-dipolar cycloaddition between heterocyclic aldehydes, amino esters and dipolaro...
1,3-Dipolar reactions of imines of both acyclic and cyclic α-amino esters with a range of nitroolefi...
Abstract: Nitrile imines generated by the oxidative dehydrogenation of aromatic aldehyde phenylhydra...
International audienceN-Metallated azomethine ylide generated from methyl (E)-N-benzylideneglycinate...
This review summarizes the trends in the formation of complex or not so complex heterocyclic structu...
textA novel application of the Pauson-Khand reaction was applied to the synthesis of a series of bri...
Centre of Advanced Studies on Natural Products including Organic Synthesis, Department of Chemistry,...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
—The regio- and diastereoselective synthesis of pyrrolidine derivatives through 1,3-dipolar cycloadd...
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