Discovery of biomimetic transamination as a general synthetic method for preparation of fluorine-containing amines and amino acids-Reference-Cited by-同舟云学术

Discovery of biomimetic transamination as a general synthetic method for preparation of fluorine-containing amines and amino acids

Published:2023-12-30 Issue:2 Volume:18 Page:3-15
ISSN:1814-9766
Container-title:Ukrainica Bioorganica Acta
language:en
Short-container-title:Ukr. Bioorg. Acta

Author:

Wzorek Alicja¹^ORCID,Han Jianlin²^ORCID,Lyutenko Nataliya V.³^ORCID,Koley Manankar⁴^ORCID,Sorochinsky Alexander E.³^ORCID,Ono Taizo⁵^ORCID

Affiliation:

1. Institute of Chemistry, Jan Kochanowski University in Kielce, Kielce, Poland

2. College of Chemical Engineering, Nanjing Forestry University, Nanjing, China

3. V.P. Kukhar Institute of Bioorganic Chemistry and Petrochemistry of the NAS of Ukraine, Kyiv, Ukraine

4. CSIR-Central Glass & Ceramic Research Institute, Kolkata, India

5. University of the Basque Country, San Sebastián, Spain; IKERBASQUE, Basque Foundation for Science, Bilbao, Spain

Abstract

In this perspective review article, we describe the discovery of azomethine-azomethine isomerization of fluorinated N-benzyl-imines and its further development into one of the most convenient, scalable, and practical synthetic methods for preparation of biologically relevant fluorinated amines and amino acids. Currently referred to as 1,3-Proton Shift Reaction, this method is widely used by organic chemists for synthesis of variety fluorinated amino compounds playing important role in the design of modern pharmaceuticals and agrochemicals

Publisher

National Academy of Sciences of Ukraine (Co. LTD Ukrinformnauka) (Publications)

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