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A Concise Synthetic Method for Constructing 3-Substituted Piperazine-2-Acetic Acid Esters from 1,2-Diamines
We report a short synthetic route for synthesizing 2,3-substituted piperazine acetic acid esters. Optically pure amino acids were efficiently converted into 1,2-diamines that could be utilized to deliver the title 2,3-substituted piperazines in five steps with a high enantiomeric purity. The novel r...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9182393/ https://www.ncbi.nlm.nih.gov/pubmed/35684357 http://dx.doi.org/10.3390/molecules27113419 |
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author | Chamakuri, Srinivas Tang, Sunny Ann Tran, Kevin A. Guduru, Shiva Krishna Reddy Bolin, Peter K. MacKenzie, Kevin R. Young, Damian W. |
author_facet | Chamakuri, Srinivas Tang, Sunny Ann Tran, Kevin A. Guduru, Shiva Krishna Reddy Bolin, Peter K. MacKenzie, Kevin R. Young, Damian W. |
author_sort | Chamakuri, Srinivas |
collection | PubMed |
description | We report a short synthetic route for synthesizing 2,3-substituted piperazine acetic acid esters. Optically pure amino acids were efficiently converted into 1,2-diamines that could be utilized to deliver the title 2,3-substituted piperazines in five steps with a high enantiomeric purity. The novel route facilitated, for the first time, the synthesis of 3-phenyl substituted-2-piperazine acetic acid esters that were difficult to achieve using other methods; however, in this case, the products underwent racemization. |
format | Online Article Text |
id | pubmed-9182393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91823932022-06-10 A Concise Synthetic Method for Constructing 3-Substituted Piperazine-2-Acetic Acid Esters from 1,2-Diamines Chamakuri, Srinivas Tang, Sunny Ann Tran, Kevin A. Guduru, Shiva Krishna Reddy Bolin, Peter K. MacKenzie, Kevin R. Young, Damian W. Molecules Article We report a short synthetic route for synthesizing 2,3-substituted piperazine acetic acid esters. Optically pure amino acids were efficiently converted into 1,2-diamines that could be utilized to deliver the title 2,3-substituted piperazines in five steps with a high enantiomeric purity. The novel route facilitated, for the first time, the synthesis of 3-phenyl substituted-2-piperazine acetic acid esters that were difficult to achieve using other methods; however, in this case, the products underwent racemization. MDPI 2022-05-25 /pmc/articles/PMC9182393/ /pubmed/35684357 http://dx.doi.org/10.3390/molecules27113419 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Chamakuri, Srinivas Tang, Sunny Ann Tran, Kevin A. Guduru, Shiva Krishna Reddy Bolin, Peter K. MacKenzie, Kevin R. Young, Damian W. A Concise Synthetic Method for Constructing 3-Substituted Piperazine-2-Acetic Acid Esters from 1,2-Diamines |
title | A Concise Synthetic Method for Constructing 3-Substituted Piperazine-2-Acetic Acid Esters from 1,2-Diamines |
title_full | A Concise Synthetic Method for Constructing 3-Substituted Piperazine-2-Acetic Acid Esters from 1,2-Diamines |
title_fullStr | A Concise Synthetic Method for Constructing 3-Substituted Piperazine-2-Acetic Acid Esters from 1,2-Diamines |
title_full_unstemmed | A Concise Synthetic Method for Constructing 3-Substituted Piperazine-2-Acetic Acid Esters from 1,2-Diamines |
title_short | A Concise Synthetic Method for Constructing 3-Substituted Piperazine-2-Acetic Acid Esters from 1,2-Diamines |
title_sort | concise synthetic method for constructing 3-substituted piperazine-2-acetic acid esters from 1,2-diamines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9182393/ https://www.ncbi.nlm.nih.gov/pubmed/35684357 http://dx.doi.org/10.3390/molecules27113419 |
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