A convenient route to optically pure α-alkyl-β-(sec-amino)alanines.

Abstract:

: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.

journal_name

Amino Acids

journal_title

Amino acids

authors

Olma A,Lasota A,Kudaj A

doi

10.1007/s00726-011-1055-3

subject

Has Abstract

pub_date

2012-06-01 00:00:00

pages

2525-8

issue

6

eissn

0939-4451

issn

1438-2199

journal_volume

42

pub_type

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