141232-76-0Relevant academic research and scientific papers
Palladium-catalyzed reduction of an allylic amine: A formal access to both diastereoisomers of cyclopentenyl glycine
Borugeois-Cury,Doan,Gore
, p. 1277 - 1280 (2007/10/02)
The easily accessible bicyclic amines 3 (exo or endo) are regioselectively transformed to the methyl esters of the diastereoisomers (1c or 1d) of N-benzyl cyclopentenylglycine by reaction with hydride donors (mainly NaBH3CN) in the presence of
