Efficient Highly Enantioselective Syntheses of (1R,2R)- and (1S,2S)-Amino- 1-alkyl(or aryl)-1,3-propanediols by Highly Stereoselective Additions and Highly Regioselective Ring Opening of Substituted Az

An Efficient Synthesis of Ephedra Alkaloid Analogues Using an Enantiomerically Pure N-(R)-(+)- -Methyl- benzylaziridine-2-carboxaldehyde

An Efficient Synthesis of Both Eantiomers of Cathinone by Regioselective Reductive Ring Opening of Substituted Aziridines

Highly Diastereoselective Reduction of Enantiomerically Pure Aziridino Ketones

N-t-Butoxycarbonyl-N-methylaminomethyllithium

Chirospecific Syntheses of Precursors of Cyclopentane and Cyclopentene Carbocyclic Nucleosides by [3+3]-Coupling and Transannular Alkylation

Regiospecific Reductive Ring Cleavage of N-Substituted Aziridine-2-carboxylates and Aziridine-2-methanol via Catalytic Hydrogenation Using Pd as a Catalyst

Chirospecific Syntheses of Precursors of Cyclopentane and Cyclopentene Carbocyclic Nucleosides

Regiospecific Reductive Ring Cleavage of N-Substituted Aziridine-2-Carboxylates

Regioselective N-Methyl Carbon Lithiation of N-Boc-Methylalkylamines. Expedient Synthesis of Unsymmetrical Amines