Development of Hamari Ligands for Practical Asymmetric Synthesis of Tailor-Made Amino Acids-Reference-Cited by-同舟云学术

Development of Hamari Ligands for Practical Asymmetric Synthesis of Tailor-Made Amino Acids

Published:2019-11-07 Issue:21 Volume:4 Page:18942-18947
ISSN:2470-1343
Container-title:ACS Omega
language:en
Short-container-title:ACS Omega

Author:

Han Jianlin¹^ORCID,Romoff Todd T.²,Moriwaki Hiroki³,Konno Hiroyuki⁴,Soloshonok Vadim A.⁵⁶^ORCID

Affiliation:

1. College of Chemical Engineering, Nanjing Forestry University, Nanjing 210037, China

2. Hamari Chemicals USA, San Diego, California 92121, United States

3. Hamari Chemicals Ltd., 1-4-29 Kunijima, Higashi-Yodogawa-ku, Osaka 533-0024, Japan

4. Department of Biochemical Engineering, Graduate School of Science and Engineering, Yamagata University, Yonezawa, Yamagata 992-8510, Japan

5. Department of Organic Chemistry I, Faculty of Chemistry, University of the Basque Country UPV/EHU, Paseo Manuel Lardizábal 3, 20018 San Sebastián, Spain

6. IKERBASQUE, Basque Foundation for Science, María Díaz de Haro 3, Plaza Bizkaia, 48013 Bilbao, Spain

Funder

Ikerbasque, Basque Foundation for Science

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acsomega.9b02940

Reference26 articles.

1. Unusual Amino Acids in Medicinal Chemistry

2. Alkylation and Michael additions of glycine ethyl ester. Use in .alpha.-amino acid synthesis and as acyl carbanion equivalent

3. Asymmetric synthesis of α-amino-acid derivatives by alkylation of a chiral Schiff base

4. Asymmetric synthesis of threonine and partial resolution and retroracemization of .alpha.-amino acids via copper(II) complexes of their Schiff bases with (S)-2-N-(N'-benzylprolyl)aminobenzaldehyde and (S)-2-N-(N'-benzylprolyl)aminoacetophenone. Crystal and molecular structure of a copper(II) complex of glycine Schiff base with (S)-2-N-(N'-benzylprolyl)aminoacetophenone

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