1343479-87-7

Upstream product

• 1343479-76-4 ethyl 2-((3R,5R)-3-(((tert-butoxycarbonyl)amino)methyl)-5-((6R,7aR)-8,8-dimethyl-2,2-dioxidohexahydro-3H-3a,6-meth-anobenzo[c]isothiazole-1-carbonyl)isoxazolidin-2-yl)acetate 
• 1343479-77-5 ethyl 2-((3R,5R)-5-(((tert-butoxycarbonyl)amino)methyl)-3-hydroxy-2-oxopyrrolidin-1-yl)acetate 
• 17257-71-5 (S)-Mosher acid 

Relevant academic research and scientific papers

Stereoselective 1,3-dipolar cycloadditions of nitrones derived from amino acids. Asymmetric synthesis of N-(alkoxycarbonylmethyl)-3-hydroxypyrrolidin-2- ones Dedicated to Professor Giovanni Romeo on occasion of his 70th birthday

Diastereoselective asymmetric 1,3-dipolar cycloadditions of N-(alkoxycarbonylmethyl) nitrones derived from glycine, alanine and phenylalanine have been studied both experimentally and theoretically. Asymmetric induction is evaluated by either introducing

High-yield synthesis of pyrrolidinyl PNA monomers

Two monomers for the syntheses of conformationally restricted peptide nucleic acids were synthesized through a simple procedure, involving an asymmetric 1,3-dipolar cycloaddition chemistry as a key step, from common starting materials in 3 and 5 steps, and 58.8% and 30.5% overall yields, respectively.