131150-38-4

Upstream product

• 917-54-4 methyllithium 
• 95437-43-7 (S)-2-(N,N-dibenzylamino)-3-phenylpropanoic acid 
• 131150-35-1 (S)-2-(dibenzylamino)-N'-methoxy-N'-methyl-3-phenylpropane amide 
• 111060-52-7 (S)-2-(dibenzylamino)-3-phenylpropan-1-ol 
• 111138-83-1 N,N-dibenzyl-L-phenylalanine benzyl ester 
• 123054-12-6 (2S)-N,N-dibenzylphenylalaninal 
• 3282-30-2 pivaloyl chloride 
• 198569-65-2 (S)-3-Dibenzylamino-4-phenyl-butan-2-ol 

Downstream Products

• 156045-58-8 (S)-5-Dibenzylamino-4-oxo-6-phenyl-hexanoic acid tert-butyl ester 
• 198569-64-1 (2S,7S)-2,7-Bis-dibenzylamino-1,8-diphenyl-octane-3,6-dione 
• 223913-37-9 (2R,3S)-3-Dibenzylamino-2,4-diphenyl-butan-2-ol 
• 223913-38-0 (2S,3S)-3-Dibenzylamino-2,4-diphenyl-butan-2-ol 
• 156045-60-2 (4S,5S)-5-Dibenzylamino-4-hydroxy-6-phenyl-hexanoic acid tert-butyl ester 
• 133333-27-4 tert-butyl (1S)-1-[(2S)-5-oxotetrahydrofuran-2-yl]-2-phenylethylcarbamate 
• 143337-98-8 (5S,1'S)-5-(1'-(dibenzylamino)-2'-phenylethyl)dihydrofuran-2(3H)-one 
• 223913-42-6 (2R,3S)-3-amino-2,4-diphenylbutan-2-ol 
• 223913-41-5 (2S,3S)-3-Amino-2,4-diphenyl-butan-2-ol 
• 130984-96-2 (2S,3S)-1-Phenyl-butane-2,3-diamine 
• 130984-46-2 (2S,3S)-N²,N²,N³-Tribenzyl-1-phenyl-butane-2,3-diamine 

Relevant academic research and scientific papers

Synthesis of a new C2-symmetric molecule with dimeric hydroxyethylene isosteric moiety

As part of our studies directed toward the development of new HIV protease inhibitors, a new type of C2-symmetric molecule having a dimeric hydroxyethylene isosteric moiety is synthesised by Cu(II)-mediated dimerisation of the sodium enolate of

NON-RACEMIZING SYNTHESIS AND STEREOSELECTIVE REDUCTION OF CHIRAL α-AMINO KETONES

α-Amino acids can be doubly benzylated at nitrogen, forming N,N-dibenzyl amino acids which can be converted into α-amino ketones 4 without appreciable racemization.The latter undergo stereoselective reduction with NaBH4 under non-chelation control to form