887128-08-7

Upstream product

• 887128-07-6 methyl (2R)-2-[benzyl(tert-butoxycarbonyl)amino]-3-hydroxypropanoate 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 100-52-7 benzaldehyde 
• 123639-56-5 methyl (2R)-2-(benzylamino)-3-hydroxypropanoate 

Downstream Products

• 887128-09-8 tert-butyl N-benzyl-N-[(1S)-1-[(tert-butyldimethylsilyloxy)methyl]-2-hydroxyethyl]carbamate 
• 134930-26-0 (S)-4-(benzylamino)-5-hydroxy-2-pentenoic acid ethyl ester 
• 887128-12-3 ((2S,3R)-1-Benzyl-2-hydroxymethyl-3a-nitro-octahydro-indol-3-yl)-acetic acid ethyl ester 
• 887128-13-4 ((2S,3S)-1-Benzyl-2-hydroxymethyl-octahydro-indol-3-yl)-acetic acid ethyl ester 
• 887128-11-2 4-(benzyl-tert-butoxycarbonyl-amino)-5-(tert-butyl-dimethyl-silanyloxy)-pent-2-enoic acid ethyl ester 

Relevant academic research and scientific papers

Orthogonally protected glycerols and 2-aminodiols: Useful building blocks in heterocyclic chemistry

The efficient synthesis of orthogonally protected glycerols, 2-aminopropane-1,3-diols and 2-aminobutane-1,4-diols that can constitute useful tools in heterocyclic chemistry, is reported. These interesting tri-functionalized small synthons were easily prepared from serine or aspartic acid. In addition, these substrates can be readily transformed into their iodide derivatives in very good yields. ARKAT USA, Inc.

Synthesis of a perhydroindolic analog of kainic acid

Synthesis of perhydroindolyl-2-carboxy-3-acetic acid, a strained analog of kainic acid, is described. This compound was obtained in 7 steps by the use of the Barco procedure from nitrocyclohexene.