143747-07-3

Upstream product

• 137649-69-5 (2S,3R,4R,5S)-2,5-bis<<(benzyloxy)carbonyl>amino>-3,4-dihydroxy-1,6-diphenylhexane 
• 122-51-0 orthoformic acid triethyl ester 
• 59830-60-3 benzyl (1S)-(1-formyl-2-phenylethyl)carbamate 
• 6372-14-1 N-((benzyloxy)carbonyl)-L-phenylalaninol 

Downstream Products

• 143747-09-5 (4S,5R,6S,1'S)-5-acetoxy-4-benzyl-6-<1-<<(benzyloxy)carbonyl>amino>-2-phenylethyl>-3,4,5,6-tetrahydro-2H-1,3-oxazin-2-one 
• 134878-07-2 (2S,3R,4S,5S)-2,5-diamino-3,4-dihydroxy-1,6-diphenylhexane 
• 143747-08-4 (2S,3R,4R,5S)-3-acetoxy-2,5-bis<<(benzyloxy)carbonyl>amino>-4-<(methanesulfonyl)oxy>-1,6-diphenylhexane 

Relevant academic research and scientific papers

Process for the preparation of a substituted diaminodiol

A process is disclosed for the preparation of a substituted diaminodiol.

Stereocontrolled Synthesis of C2-Symmetric and Pseudo-C2-Symmetric Diamino Alcohols and Diols for Use in HIV Protease Inhibitors

The stereocontrolled syntheses of dibenzyldiamino alcohol 1 and dibenzyldiamino diols 2-4, core units of potent C2-symmetric and pseudo-C2-symmetric inhibitors of HIV protease, are described, starting from phenylalanine.Stereoselecti