DOIAbstract
Cyclic amidines are prepared in 3 steps from an aromatic aldehyde, isobutyraldehyde, and urea. The amidines 1 and 2 are readily resolved using chiral cyclic phosphoric acids
Cyclic amidines are prepared in 3 steps from an aromatic aldehyde, isobutyraldehyde, and urea. The amidines 1 and 2 are readily resolved using chiral cyclic phosphoric acids
The syntheses of new chiral cyclic 1,2-diacetals from (2R, 3R)-( )-tartaric acidare described. C2-sy...
© 2020 Wiley Periodicals LLC. Imine is one of the most versatile functional groups in chemistry and ...
The palladium catalysed insertion of isonitriles into aryl bromides carrying pendant amine or alcoho...
Cyclic amidines are prepared in 3 steps from an aromatic aldehyde, isobutyraldehyde, and urea. The a...
A facile access to optically active cyclic ureas was developed through palladium-catalyzed asymmetri...
Radical cyclization of amide substrates was performed to establish the Memory of Chirality (MOC). Am...
Chiral induction was utilized for the synthesis of diastereopure cyclic peptoids containing an N-ben...
In extending our studies involving BF3-Et(2)O-catalyzed reaction of cinnamic acid analogues, we have...
Part I. Cationic cyclization reactions of unsaturated amides were studied. Several different unsatur...
The regioselective nucleophilic reactivity of cyclic amidines is considered in the context of their ...
Recyclable chiral diamine–polyoxometalate (POM) acids catalyzed asymmetric direct aldol reaction of ...
Primary and secondary aliphatic and saturated cyclic amines as well as primary aromatic and heterocy...
Abstract A general procedure for the synthesis of amides via the direct condensation of carboxylic a...
Synthesis of new beta-lactams is an attractive field because some of these types of molecules are bi...
A novel route into chiral amides is achieved through the efficient, non-racemising, cleavage of N-ac...
The syntheses of new chiral cyclic 1,2-diacetals from (2R, 3R)-( )-tartaric acidare described. C2-sy...
© 2020 Wiley Periodicals LLC. Imine is one of the most versatile functional groups in chemistry and ...
The palladium catalysed insertion of isonitriles into aryl bromides carrying pendant amine or alcoho...
Cyclic amidines are prepared in 3 steps from an aromatic aldehyde, isobutyraldehyde, and urea. The a...
A facile access to optically active cyclic ureas was developed through palladium-catalyzed asymmetri...
Radical cyclization of amide substrates was performed to establish the Memory of Chirality (MOC). Am...
Chiral induction was utilized for the synthesis of diastereopure cyclic peptoids containing an N-ben...
In extending our studies involving BF3-Et(2)O-catalyzed reaction of cinnamic acid analogues, we have...
Part I. Cationic cyclization reactions of unsaturated amides were studied. Several different unsatur...
The regioselective nucleophilic reactivity of cyclic amidines is considered in the context of their ...
Recyclable chiral diamine–polyoxometalate (POM) acids catalyzed asymmetric direct aldol reaction of ...
Primary and secondary aliphatic and saturated cyclic amines as well as primary aromatic and heterocy...
Abstract A general procedure for the synthesis of amides via the direct condensation of carboxylic a...
Synthesis of new beta-lactams is an attractive field because some of these types of molecules are bi...
A novel route into chiral amides is achieved through the efficient, non-racemising, cleavage of N-ac...
The syntheses of new chiral cyclic 1,2-diacetals from (2R, 3R)-( )-tartaric acidare described. C2-sy...
© 2020 Wiley Periodicals LLC. Imine is one of the most versatile functional groups in chemistry and ...
The palladium catalysed insertion of isonitriles into aryl bromides carrying pendant amine or alcoho...
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