Add to ORKGDipolar 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 pyrazolidine
Azomethine ylides derived from 3,4-dihydropyrrolo[1,2-a]pyrazinium salts undergo 1,3-dipolar cycload...
Azomethine ylides derived from 3,4-dihydropyrrolo[1,2-a]pyrazinium salts undergo 1,3-dipolar cycload...
Azomethine ylides derived from 3,4-dihydropyrrolo[1,2-a]pyrazinium salts undergo 1,3-dipolar cycload...
Dipolar cycloadditions of azomethine imines, formed in situ from aldehydes and N1-alkyl-N2-acylhydra...
1,3-Dipolar reactions of imines of both acyclic and cyclic α-amino esters with a range of nitroolefi...
Azomethine imines are considered 1,3-dipoles of the aza-allyl type which are transient intermediates...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
1,3-Dipolar reactions of imines of both acyclic and cyclic α-amino esters with a range of nitroolefi...
In recent years, the design and synthesis of structures that can potentially mimic the properties of...
A multicomponent 1,3-dipolar cycloaddition between heterocyclic aldehydes, amino esters and dipolaro...
Azomethine ylides derived from 3,4-dihydropyrrolo[1,2-a]pyrazinium salts undergo 1,3-dipolar cycload...
Azomethine ylides derived from 3,4-dihydropyrrolo[1,2-a]pyrazinium salts undergo 1,3-dipolar cycload...
Azomethine ylides derived from 3,4-dihydropyrrolo[1,2-a]pyrazinium salts undergo 1,3-dipolar cycload...
Dipolar cycloadditions of azomethine imines, formed in situ from aldehydes and N1-alkyl-N2-acylhydra...
1,3-Dipolar reactions of imines of both acyclic and cyclic α-amino esters with a range of nitroolefi...
Azomethine imines are considered 1,3-dipoles of the aza-allyl type which are transient intermediates...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
1,3-Dipolar reactions of imines of both acyclic and cyclic α-amino esters with a range of nitroolefi...
In recent years, the design and synthesis of structures that can potentially mimic the properties of...
A multicomponent 1,3-dipolar cycloaddition between heterocyclic aldehydes, amino esters and dipolaro...
Azomethine ylides derived from 3,4-dihydropyrrolo[1,2-a]pyrazinium salts undergo 1,3-dipolar cycload...
Azomethine ylides derived from 3,4-dihydropyrrolo[1,2-a]pyrazinium salts undergo 1,3-dipolar cycload...
Azomethine ylides derived from 3,4-dihydropyrrolo[1,2-a]pyrazinium salts undergo 1,3-dipolar cycload...