Add to ORKGThe sodium salt of sulfimide 2 is a useful asymmetric methylidene transfer agent for the synthesis of enantiomerically enriched epoxides and aziridines. Moderate enantioselectivities are observed with a broad range of carbonyl compounds and with imines. An enantiomerically enriched beta-adrenoreceptor agonist analogue was prepared using the new method
Aziridines, the nitrogenous analogues of epoxides, are useful building blocks for the synthesis of v...
A synthetic strategy to obtain new enantiopure trans-3,4-diaminocaranes derived from (+)-3-carene vi...
Ephedrine can be readily converted by means of intramolecular S(N)2 substitution by the hydroxyl or ...
Enantiomerically enriched sulfimides are used to prepare enantiomerically enriched epoxides, aziridi...
Enantioselective transfer hydrogenation of a-amino ketones is an effective method for the asymmetric...
Chiral cyclic and acyclic allyl aminosulfoxonium ylides have been generated from aminosulfoxonium-su...
The enantiomerically pure title aziridines were obtained by regioselective azidolysis of the 2',3'-e...
Ephedrine and pseudoephedrine are converted by means of a Mitsunobu reaction to respectively trans- ...
Two different routes for the regio- and stereoslective synthesis of aziridino epoxides from cyclic d...
The sodium salt of (S)-sulfimide 8 reacts with carbonyl compounds to yield (R)-epoxides in 60-64% yi...
A rapid, expedient and enantioselective method for the synthesis of beta-hydroxy amines and monosubs...
A rapid, expedient and enantioselective method for the synthesis of beta-hydroxy amines and monosubs...
A rapid, expedient and enantioselective method for the synthesis of beta-hydroxy amines and monosubs...
Two different routes for the regio- and stereoslective synthesis of aziridino epoxides from cyclic d...
A synthetic strategy to obtain new enantiopure trans-3,4-diaminocaranes derived from (+)-3-carene vi...
Aziridines, the nitrogenous analogues of epoxides, are useful building blocks for the synthesis of v...
A synthetic strategy to obtain new enantiopure trans-3,4-diaminocaranes derived from (+)-3-carene vi...
Ephedrine can be readily converted by means of intramolecular S(N)2 substitution by the hydroxyl or ...
Enantiomerically enriched sulfimides are used to prepare enantiomerically enriched epoxides, aziridi...
Enantioselective transfer hydrogenation of a-amino ketones is an effective method for the asymmetric...
Chiral cyclic and acyclic allyl aminosulfoxonium ylides have been generated from aminosulfoxonium-su...
The enantiomerically pure title aziridines were obtained by regioselective azidolysis of the 2',3'-e...
Ephedrine and pseudoephedrine are converted by means of a Mitsunobu reaction to respectively trans- ...
Two different routes for the regio- and stereoslective synthesis of aziridino epoxides from cyclic d...
The sodium salt of (S)-sulfimide 8 reacts with carbonyl compounds to yield (R)-epoxides in 60-64% yi...
A rapid, expedient and enantioselective method for the synthesis of beta-hydroxy amines and monosubs...
A rapid, expedient and enantioselective method for the synthesis of beta-hydroxy amines and monosubs...
A rapid, expedient and enantioselective method for the synthesis of beta-hydroxy amines and monosubs...
Two different routes for the regio- and stereoslective synthesis of aziridino epoxides from cyclic d...
A synthetic strategy to obtain new enantiopure trans-3,4-diaminocaranes derived from (+)-3-carene vi...
Aziridines, the nitrogenous analogues of epoxides, are useful building blocks for the synthesis of v...
A synthetic strategy to obtain new enantiopure trans-3,4-diaminocaranes derived from (+)-3-carene vi...
Ephedrine can be readily converted by means of intramolecular S(N)2 substitution by the hydroxyl or ...