1384954-86-2Relevant academic research and scientific papers
A convenient route to optically pure α-alkyl-β-(sec-amino) alanines
Olma,Lasota,Kudaj
, p. 2525 - 2528 (2012/07/27)
The cyclization of N-Boc-α-alkylserines to corresponding β-lactones under Mitsunobu reaction conditions and the ring opening with heterocyclic amines (pyrrolidine, piperidine, morpholine and thiomorpholine) produced N-Boc-α-alkyl-β-(sec-amino)alanines. The removal of the Boc group gives di-hydrochlorides of non-protein amino acids.
