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Comparative study of different chiral ligands for dynamic kinetic resolution of amino acids.
Nagaoka, Keita; Nakano, Arina; Han, Jianlin; Sakamoto, Tsubasa; Konno, Hiroyuki; Moriwaki, Hiroki; Abe, Hidenori; Izawa, Kunisuke; Soloshonok, Vadim A.
Afiliação
  • Nagaoka K; Department of Biological Engineering, Graduate School of Science and Engineering, Yamagata University, Yonezawa, Yamagata, Japan.
  • Nakano A; Department of Biological Engineering, Graduate School of Science and Engineering, Yamagata University, Yonezawa, Yamagata, Japan.
  • Han J; Jiangsu Co-Innovation Center of Efficient Processing and Utilization of Forest Resources, College of Chemical Engineering, Nanjing Forestry University, Nanjing, China.
  • Sakamoto T; Hamari Chemicals Ltd., Osaka, Japan.
  • Konno H; Department of Biological Engineering, Graduate School of Science and Engineering, Yamagata University, Yonezawa, Yamagata, Japan.
  • Moriwaki H; Hamari Chemicals Ltd., Osaka, Japan.
  • Abe H; Hamari Chemicals Ltd., Osaka, Japan.
  • Izawa K; Hamari Chemicals Ltd., Osaka, Japan.
  • Soloshonok VA; Department of Organic Chemistry I, Faculty of Chemistry, University of the Basque Country UPV/EHU, San Sebastián, Spain.
Chirality ; 33(10): 685-702, 2021 10.
Article em En | MEDLINE | ID: mdl-34402557
ABSTRACT
Dynamic kinetic resolution (DKR) of unprotected amino acids (AAs), via intermediate formation of Ni(II) complexes, is currently a leading methodology for preparation of natural and tailor-made AAs in enantiomerically pure form. In this work, we conduct a comparative case study of synthetic performance of four different ligands in DKR of six AAs representing aryl-, benzyl-, alkyl-, and long alkyl-type derivatives. The results of this study allow for rational selection of ligand/AA type to develop a practical procedure for preparation of target enantiomerically pure AAs.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aminoácidos / Níquel Idioma: En Revista: Chirality Assunto da revista: BIOLOGIA MOLECULAR / QUIMICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aminoácidos / Níquel Idioma: En Revista: Chirality Assunto da revista: BIOLOGIA MOLECULAR / QUIMICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Japão