This review highlights the biological importance of many polysubstituted nitro-prolines and -pyrrolidines. Their preparation using asymmetric 1,3-dipolar cycloadditions of azomethine ylides with nitroalkenes using diastereoselective and enantioselective strategies is described remarking the scope and main features of each one.This work has been supported by the Spanish Ministerio de Economía y Competitividad (MINECO) (Consolider INGENIO 2010 CSD2007-00006, CTQ2010-20387), FEDER, Generalitat Valenciana (PROMETEO/2009/039), and by the University of Alicante
Enantiomerically pure (E)-gamma-alkoxy-alpha,beta-unsaturated esters were reacted with azomethine yl...
Two complementary approaches to substituted pyrrolidines via stereocontrolled 1,3-dipolar cycloaddit...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
This review highlights the biological importance of many polysubstituted nitro-prolines and -pyrroli...
CONSPECTUS: Cycloaddition reactions are among the most powerful methods for the synthesis of complex...
Enantiopure exo-4-nitro-3,5-diphenylproline reacts with aldehydes and electrophilic alkenes, in good...
International audienceThe use of structurally similar chiral non-racemic azomethine ylides, nitrones...
The pyrrolidine ring is a privileged structural motif in synthetic and medicinal chemisty. This revi...
International audienceThe use of structurally similar chiral non-racemic azomethine ylides, nitrones...
This review summarizes the trends in the formation of complex or not so complex heterocyclic structu...
The (3+2) cycloaddition between azomethine ylides and alkenes is an efficient, convergent and stereo...
Enantiopure exo-4-nitro-3,5-diphenylproline reacts with aldehydes and electrophilic alkenes, in good...
Catalytic asymmetric 1,3-dipolar cycloadditions of azomethine ylides have turned out to be one of th...
A series of chiral <i>N,O</i>-ligands derived from a 1,2-dihydroimidazo[1,2-<i>a</i>]quinolone mo...
A series of chiral <i>N,O</i>-ligands derived from a 1,2-dihydroimidazo[1,2-<i>a</i>]quinolone mo...
Enantiomerically pure (E)-gamma-alkoxy-alpha,beta-unsaturated esters were reacted with azomethine yl...
Two complementary approaches to substituted pyrrolidines via stereocontrolled 1,3-dipolar cycloaddit...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
This review highlights the biological importance of many polysubstituted nitro-prolines and -pyrroli...
CONSPECTUS: Cycloaddition reactions are among the most powerful methods for the synthesis of complex...
Enantiopure exo-4-nitro-3,5-diphenylproline reacts with aldehydes and electrophilic alkenes, in good...
International audienceThe use of structurally similar chiral non-racemic azomethine ylides, nitrones...
The pyrrolidine ring is a privileged structural motif in synthetic and medicinal chemisty. This revi...
International audienceThe use of structurally similar chiral non-racemic azomethine ylides, nitrones...
This review summarizes the trends in the formation of complex or not so complex heterocyclic structu...
The (3+2) cycloaddition between azomethine ylides and alkenes is an efficient, convergent and stereo...
Enantiopure exo-4-nitro-3,5-diphenylproline reacts with aldehydes and electrophilic alkenes, in good...
Catalytic asymmetric 1,3-dipolar cycloadditions of azomethine ylides have turned out to be one of th...
A series of chiral <i>N,O</i>-ligands derived from a 1,2-dihydroimidazo[1,2-<i>a</i>]quinolone mo...
A series of chiral <i>N,O</i>-ligands derived from a 1,2-dihydroimidazo[1,2-<i>a</i>]quinolone mo...
Enantiomerically pure (E)-gamma-alkoxy-alpha,beta-unsaturated esters were reacted with azomethine yl...
Two complementary approaches to substituted pyrrolidines via stereocontrolled 1,3-dipolar cycloaddit...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...