HAMARI’S CONTRIBUTION TO THE ASYMMETRIC SYNTHESIS OF TAILOR-MADE AMINO ACIDS

This article reviews the development of the asymmetric synthesis of tailor-made amino acids conducted at Hamari Chemicals during the 10-year period 2013–2022.The discussion is based on strategies such as direct chiral modification of unprotected amino acids via intermediate formation of Ni(II) compl...

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Date:2024
Main Authors: Han, Jianlin, Liu, Hong, Wang, Jiang, Wzorek, Alicja, Sorochinsky, Alexander, Klika, Karel, Ono, Taizo, Moriwaki, Hiroki, Sato, Tatsunori, Kunisuke , Izawa, Konno, Hiroyuki, Soloshonok, Vadim
Format: Article
Language:English
Published: V.I.Vernadsky Institute of General and Inorganic Chemistry 2024
Online Access:https://ucj.org.ua/index.php/journal/article/view/693
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Journal Title:Ukrainian Chemistry Journal

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Ukrainian Chemistry Journal
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spelling oai:ojs2.1444248.nisspano.web.hosting-test.net:article-6932025-03-26T18:07:37Z HAMARI’S CONTRIBUTION TO THE ASYMMETRIC SYNTHESIS OF TAILOR-MADE AMINO ACIDS Han, Jianlin Liu, Hong Wang, Jiang Wzorek, Alicja Sorochinsky, Alexander Klika, Karel Ono, Taizo Moriwaki, Hiroki Sato, Tatsunori Kunisuke , Izawa Konno, Hiroyuki Soloshonok, Vadim tailor-made amino acids; drug design and development; second-order asymmetric transformation; dynamic kinetic resolution; inversion of chirality. This article reviews the development of the asymmetric synthesis of tailor-made amino acids conducted at Hamari Chemicals during the 10-year period 2013–2022.The discussion is based on strategies such as direct chiral modification of unprotected amino acids via intermediate formation of Ni(II) complexes and elaboration of chiral nucleophilic or electrophilic glycine equivalents. The former approach includes, for example, second-order asymmetric transformation, dynamic kinetic resolution, and inversion of chirality while the latter approach involves construction of the desired amino acid architecture using, for example, alkylation, aldol, Mannich, or Michael addition reactions as well as multistep procedures. Operational convenience, scalability, and practicality of the developed methods are emphasized. V.I.Vernadsky Institute of General and Inorganic Chemistry 2024-11-29 Article Article Organic chemistry Органическая xимия Органічна xімія application/pdf https://ucj.org.ua/index.php/journal/article/view/693 10.33609/2708-129X.90.10.2024.88-134 Ukrainian Chemistry Journal; Vol. 90 No. 10 (2024): Ukrainian Chemistry Journal; 88-134 Украинский химический журнал; Том 90 № 10 (2024): Ukrainian Chemistry Journal; 88-134 Український хімічний журнал; Том 90 № 10 (2024): Ukrainian Chemistry Journal; 88-134 2708-129X 2708-1281 en https://ucj.org.ua/index.php/journal/article/view/693/346
institution Ukrainian Chemistry Journal
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datestamp_date 2025-03-26T18:07:37Z
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language English
topic_facet tailor-made amino acids
drug design and development
second-order asymmetric transformation
dynamic kinetic resolution
inversion of chirality.
format Article
author Han, Jianlin
Liu, Hong
Wang, Jiang
Wzorek, Alicja
Sorochinsky, Alexander
Klika, Karel
Ono, Taizo
Moriwaki, Hiroki
Sato, Tatsunori
Kunisuke , Izawa
Konno, Hiroyuki
Soloshonok, Vadim
spellingShingle Han, Jianlin
Liu, Hong
Wang, Jiang
Wzorek, Alicja
Sorochinsky, Alexander
Klika, Karel
Ono, Taizo
Moriwaki, Hiroki
Sato, Tatsunori
Kunisuke , Izawa
Konno, Hiroyuki
Soloshonok, Vadim
HAMARI’S CONTRIBUTION TO THE ASYMMETRIC SYNTHESIS OF TAILOR-MADE AMINO ACIDS
author_facet Han, Jianlin
Liu, Hong
Wang, Jiang
Wzorek, Alicja
Sorochinsky, Alexander
Klika, Karel
Ono, Taizo
Moriwaki, Hiroki
Sato, Tatsunori
Kunisuke , Izawa
Konno, Hiroyuki
Soloshonok, Vadim
author_sort Han, Jianlin
title HAMARI’S CONTRIBUTION TO THE ASYMMETRIC SYNTHESIS OF TAILOR-MADE AMINO ACIDS
title_short HAMARI’S CONTRIBUTION TO THE ASYMMETRIC SYNTHESIS OF TAILOR-MADE AMINO ACIDS
title_full HAMARI’S CONTRIBUTION TO THE ASYMMETRIC SYNTHESIS OF TAILOR-MADE AMINO ACIDS
title_fullStr HAMARI’S CONTRIBUTION TO THE ASYMMETRIC SYNTHESIS OF TAILOR-MADE AMINO ACIDS
title_full_unstemmed HAMARI’S CONTRIBUTION TO THE ASYMMETRIC SYNTHESIS OF TAILOR-MADE AMINO ACIDS
title_sort hamari’s contribution to the asymmetric synthesis of tailor-made amino acids
description This article reviews the development of the asymmetric synthesis of tailor-made amino acids conducted at Hamari Chemicals during the 10-year period 2013–2022.The discussion is based on strategies such as direct chiral modification of unprotected amino acids via intermediate formation of Ni(II) complexes and elaboration of chiral nucleophilic or electrophilic glycine equivalents. The former approach includes, for example, second-order asymmetric transformation, dynamic kinetic resolution, and inversion of chirality while the latter approach involves construction of the desired amino acid architecture using, for example, alkylation, aldol, Mannich, or Michael addition reactions as well as multistep procedures. Operational convenience, scalability, and practicality of the developed methods are emphasized.
publisher V.I.Vernadsky Institute of General and Inorganic Chemistry
publishDate 2024
url https://ucj.org.ua/index.php/journal/article/view/693
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