160235-14-3

Upstream product

• 160235-09-6 {(S)-1-[(S)-1-(Methoxy-methyl-carbamoyl)-2-phenyl-ethylcarbamoyl]-2-methyl-propyl}-carbamic acid tert-butyl ester 
• 87694-53-9 Boc-Phe-OH N,O-dimethyl hydroxamate 
• 145525-25-3 tert-butyl ((S)-3-methyl-1-oxo-1-(((S)-1-oxo-3-phenylpropan-2-yl)amino)butan-2-yl)carbamate 
• 17435-72-2 ethyl 2-bromomethyl-2-propenoate 
• 133489-47-1 (S)-2-amino-N-methoxy-N-methyl-3-phenylpropanamide 
• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 13734-41-3 t-Boc-L-valine 

Relevant academic research and scientific papers

CrCl2 mediated addition of allylic halides or phosphates to N-protected α-amino aldehydes. Stereocontrolled synthesis of a new core for C2 symmetric HIV-protease inhibitors

The addition of γ-monosubstituted allylchromium(III) reagents to N-protected α-amino aldehydes proceeds in a stereoconvergent manner in contrast with the case of the unsubstituted reagents, where the stereoselectivity depends on the nature of the group bo

CrCl2 mediated allylation of N-protected α-amino aldehydes. A versatile synthesis of polypeptides containing an hydroxyethylene isostere

Differently substituted allylic bromides react with N-protected amino aldehydes to give intermediate products for the synthesis of hydroxyethylene dipeptide isosteres. The low stereoselectivity of this reaction can be improved using aldehydes protected wi