132903-68-5

Upstream product

• 100-52-7 benzaldehyde 
• 90048-49-0 tert-butyl (2S)-2-amino-3-hydroxypropanoate 
• 132903-69-6 N-benzyl-(2R,S)-oxo-1,2,3-oxathiazolidine-(4S)-carboxylic acid tert-butyl ester 
• 132903-70-9 N-benzyl-2,2-dioxo-1,2,3-oxathiazolidine-(4S)-carboxylic acid tert-butyl ester 
• 1026455-46-8 (S)-2-benzylamino-3-(tert-butyldimethylsilyloxy)propionic acid 
• 106910-76-3 (S)-2-(benzylamino)-3-hydroxypropanoic acid 
• 132903-76-5 (S)-2-Benzylamino-3-(tert-butyl-dimethyl-silanyloxy)-propionic acid tert-butyl ester 

Downstream Products

• 1415318-24-9 N-benzyl-2-(4-hydroxybenzamido)tert-butylacrylate 
• 1415318-30-7 C₁₇H₁₃NO₄ 
• 132903-69-6 N-benzyl-(2R)-oxo-1,2,3-oxathiazolidine-(4S)-carboxylic acid tert-butyl ester 
• 132958-54-4 N-benzyl-(2S)-oxo-1,2,3-oxathiazolidine-(4S)-carboxylic acid tert-butyl ester 

Relevant academic research and scientific papers

TRIAZOLE-ISOXAZOLE COMPOUND AND MEDICAL USE THEREOF

A compound represented by Formula [I]: or pharmaceutically acceptable salt thereof, wherein each symbol is as defined in the description.

A hypervalent iodine-mediated spirocyclization of 2-(4-hydroxybenzamido) acrylates - Unexpected formation of δ-spirolactones

On the way towards a new total synthesis of (S)-arogenate, a novel aryl-λ3-iodane-mediated oxidative spirocyclization of para-substituted phenol derivatives has been discovered. Starting from easy accessible 2-(4-hydroxybenzamido)acrylates we c

Cyclic sulphamidates: New synthetic precursors for β-functionalised α-amino acids

The nucleophilic ring opening of cyclic sulphamidates derived from (S)-serine by a variety of nucleophiles, was utilised in a novel approach to the synthesis of β-substituted alanines.