161815-94-7

Upstream product

• 161758-23-2 (4S,5S)-5-((tert-Butoxycarbonyl)amino)-1-chloro-6-phenyl-2-((trimethylsilyl)methyl)-1-hexen-4-ol 
• 161758-60-7 (4S,5S)-4-Benzyl-3-(tert-butoxycarbonyl)-5-(2-formyl-3-propenyl)-2,2-dimethyl-1,3-oxazolidine 
• 143006-56-8 (4S,5S)-4-benzyl-3-(tert-butoxycarbonyl)-5-(2-(chloromethyl)-3-propenyl)-2,2-dimethyl-1,3-oxazolidine 
• 143006-54-6 (4S,5S)-5-((tert-butoxycarbonyl)amino)-2-(chloromethyl)-6-phenyl-1-hexen-4-ol 
• 72155-45-4 Boc-L-phenylalaninal 
• 161758-24-3 (4S,5S)-4-Benzyl-3-(tert-butoxycarbonyl)-2,2-dimethyl-5-(2-methylene-4-phenyl-4(E)-butenyl)-1,3-oxazolidine 

Downstream Products

• 161758-52-7 (4S,5S)-4-Benzyl-3-(tert-butoxycarbonyl)-2,2-dimethyl-5-(2(S)-carboxy-4-phenyl-4(E)-butenyl)-1,3-oxazolidine 
• 161758-53-8 (3S,5S,6S)-6-((tert-butoxycarbonyl)amino)-3-carboxy-1,7-diphenyl-1(E)-hepten-5-ol 
• 161758-55-0 (4S,5S)-4-Benzyl-5-[(E)-(S)-2-((1S,2R)-2-hydroxy-indan-1-ylcarbamoyl)-4-phenyl-but-3-enyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 161758-51-6 (4S,5S)-4-Benzyl-5-((E)-(S)-2-formyl-4-phenyl-but-3-enyl)-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 

Relevant academic research and scientific papers

Stereoselective 'ene' reaction of allylsilanes with amino aldehydes. An application to the synthesis of potential HIV-1 protease inhibitors

2-Substituted 3-(trimethylsilyl)-1-propenes react with N-Doc-α-amino aldehydes in the presence of BF3·OEt2 to give homoallylic alcohols, potential intermediates for the synthesis of hydroxyethylene peptide isosteres. The reaction giv