130157-08-3

Upstream product

• 130157-00-5 (Benzhydrylidene-amino)-acetic acid (1R,2S,4S)-1-[(dicyclohexylsulfamoyl)-methyl]-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester 
• 130195-81-2 Azido-acetic acid (1R,2S,4S)-1-[(dicyclohexylsulfamoyl)-methyl]-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester 
• 130195-80-1 Chloro-acetic acid (1R,2S,4S)-1-[(dicyclohexylsulfamoyl)-methyl]-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester 
• 130178-50-6 Amino-acetic acid (1R,2S,4S)-1-[(dicyclohexylsulfamoyl)-methyl]-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester 
• 99295-72-4 (+)-(1R,2S,4S)-N,N-dicyclohexyl-7,7-dimethyl-2-hydroxybicyclo[2.2.1]heptane-1-methanesulfonamide 
• 130272-36-5 Amino-acetic acid (1R,2S,4S)-1-[(dicyclohexylsulfamoyl)-methyl]-7,7-dimethyl-bicyclo[2.2.1]hept-2-yl ester; hydrochloride 
• 1013-88-3 Benzophenone imine 

Relevant academic research and scientific papers

Double asymmetric synthesis: Palladium chiral complexes in the alkylation of chiral schiff bases derived from glycine

A new double asymmetric induction in carbon-carbon bond formation is achieved by the use of palladium chiral complexes in the alkylation of chiral Schiff bases 1 derived from glycine. High diastereoisomeric excesses are obtained (90-99%) using N,N-cyclohe