107114-01-2Relevant academic research and scientific papers
Pyrrolidine-Forming 1,3-Dipolar Cycloaddition of N-(Phenylthiomethyl)-α-amino Acid Esters
Imai, Nobuyuki,Nemoto, Mari,Terao, Yoshiyasu,Achiwa, Kazuo,Sekiya, Minoru
, p. 1080 - 1088 (2007/10/02)
The sodium hydride-aided reaction of N-(phenylthiomethyl)-α-amino acid esters with α,β-unsaturated carboxylates results in a pyrrolidine-forming 1,3-dipolar cycloaddition.Thus, a new route to pyrrolidines, pyrrolizidines and indolizidines has been provide
