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Chiral auxiliary recycling in continuous flow: automated recovery and reuse of Oppolzer's sultam
The telescoping of a three-stage, chiral auxiliary-mediated transformation in flow is described, including continuous separation of the product and auxiliary. The auxiliary can either be collected for later reuse, or directly fed back to the beginning of the process for recycling in real time, enabl...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5896371/ https://www.ncbi.nlm.nih.gov/pubmed/29719686 http://dx.doi.org/10.1039/c7sc05192a |
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author | Sullivan, R. J. Newman, S. G. |
author_facet | Sullivan, R. J. Newman, S. G. |
author_sort | Sullivan, R. J. |
collection | PubMed |
description | The telescoping of a three-stage, chiral auxiliary-mediated transformation in flow is described, including continuous separation of the product and auxiliary. The auxiliary can either be collected for later reuse, or directly fed back to the beginning of the process for recycling in real time, enabling each molecule of auxiliary to make multiple equivalents of chiral product and thus minimizing the step- and atom-economy issues associated with auxiliary-mediated synthesis. This concept is demonstrated for the asymmetric hydrogenation of olefins using Oppolzer's sultam, shortening the total reaction time >100 fold compared to batch, and demonstrating formal sub-stoichiometric auxiliary loading with respect to the process by automating auxiliary recycling within a closed loop. |
format | Online Article Text |
id | pubmed-5896371 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-58963712018-05-01 Chiral auxiliary recycling in continuous flow: automated recovery and reuse of Oppolzer's sultam Sullivan, R. J. Newman, S. G. Chem Sci Chemistry The telescoping of a three-stage, chiral auxiliary-mediated transformation in flow is described, including continuous separation of the product and auxiliary. The auxiliary can either be collected for later reuse, or directly fed back to the beginning of the process for recycling in real time, enabling each molecule of auxiliary to make multiple equivalents of chiral product and thus minimizing the step- and atom-economy issues associated with auxiliary-mediated synthesis. This concept is demonstrated for the asymmetric hydrogenation of olefins using Oppolzer's sultam, shortening the total reaction time >100 fold compared to batch, and demonstrating formal sub-stoichiometric auxiliary loading with respect to the process by automating auxiliary recycling within a closed loop. Royal Society of Chemistry 2018-01-25 /pmc/articles/PMC5896371/ /pubmed/29719686 http://dx.doi.org/10.1039/c7sc05192a Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0) |
spellingShingle | Chemistry Sullivan, R. J. Newman, S. G. Chiral auxiliary recycling in continuous flow: automated recovery and reuse of Oppolzer's sultam |
title | Chiral auxiliary recycling in continuous flow: automated recovery and reuse of Oppolzer's sultam
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title_full | Chiral auxiliary recycling in continuous flow: automated recovery and reuse of Oppolzer's sultam
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title_fullStr | Chiral auxiliary recycling in continuous flow: automated recovery and reuse of Oppolzer's sultam
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title_full_unstemmed | Chiral auxiliary recycling in continuous flow: automated recovery and reuse of Oppolzer's sultam
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title_short | Chiral auxiliary recycling in continuous flow: automated recovery and reuse of Oppolzer's sultam
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title_sort | chiral auxiliary recycling in continuous flow: automated recovery and reuse of oppolzer's sultam |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5896371/ https://www.ncbi.nlm.nih.gov/pubmed/29719686 http://dx.doi.org/10.1039/c7sc05192a |
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