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Chemical Dynamic Thermodynamic Resolution and S/R Interconversion of Unprotected Unnatural Tailor-made α-Amino Acids
Author(s) -
Shuni Wang,
Shengbin Zhou,
Jiang Wang,
Yong Nian,
Aki Kawashima,
Hiroki Moriwaki,
José Luis Aceña,
Vadim A. Soloshonok,
Hong Liu
Publication year - 2015
Publication title -
the journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.2
H-Index - 228
eISSN - 1520-6904
pISSN - 0022-3263
DOI - 10.1021/acs.joc.5b01292
Subject(s) - chemistry , combinatorial chemistry , generality , computational chemistry , organic chemistry , psychology , psychotherapist
Described here is an advanced, general method for purely chemical dynamic thermodynamic resolution and S/R interconversion of unprotected tailor-made α-amino acids (α-AAs) through intermediate formation of the corresponding nickel(II)-chelated Schiff bases. The method features virtually complete stereochemical outcome, broad substrate generality (35 examples), and operationally convenient conditions allowing for large-scale preparation of the target α-AAs in enantiomerically pure form. Furthermore, the new type of nonracemizable axially chiral ligands can be quantitatively recycled and reused, rendering the whole process economically and synthetically attractive.

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