296782-38-2

Upstream product

• 296782-36-0 (2S,5R)-5-(tert-Butyl-dimethyl-silanyloxymethyl)-1-(2,2,2-trifluoro-acetyl)-pyrrolidine-2-carboxylic acid tert-butyl ester 
• 296782-34-8 1-benzyl-5-(tert-butyl-dimethyl-silanyloxymethyl)-pyrrolidine-2-carboxylic acid tert-butyl ester 
• 296782-37-1 (2S,5R)-5-Hydroxymethyl-1-(2,2,2-trifluoro-acetyl)-pyrrolidine-2-carboxylic acid tert-butyl ester 
• 296782-35-9 5-(tert-butyl-dimethyl-silanyloxymethyl)-pyrrolidine-2-carboxylic acid tert-butyl ester 
• 296782-15-5 (2S,5R)-5-Formyl-1-(2,2,2-trifluoro-acetyl)-pyrrolidine-2-carboxylic acid tert-butyl ester 
• 183996-24-9 (2S,5S)-1-benzyl-5-hydroxymethylpyrrolidine-2-carboxylic acid tert-butyl ester 
• 24424-99-5 di-tert-butyl dicarbonate 
• 296782-55-3 (2S,5R)-5-((Z)-2-Benzyloxycarbonylamino-2-methoxycarbonyl-vinyl)-1-(2,2,2-trifluoro-acetyl)-pyrrolidine-2-carboxylic acid tert-butyl ester 

Relevant academic research and scientific papers

Synthesis of azabicycloalkane amino acid scaffolds as reverse-turn inducer dipeptide mimics

In an effort to design dipeptide structural mimics of protein and peptide reverse-turns, a series of 5,5-, 6,5-, and 7,5-fused 2-oxo-1- azabicycloalkane amino acids has been synthesized. A new and convenient synthetic route utilizing a Horner-Emmons react