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Enantioselective Synthesis of a New Non-Natural Gabosine
The preparation of a new non-natural gabosine is reported, in which the chirality is transferred from the toluene’s biotransformed metabolite (1R,2S)-3-methylcyclohexa-3.5-diene-1,2-diol. Further chemical transformations to introduce additional functionality and chirality to the molecule were also a...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7961443/ https://www.ncbi.nlm.nih.gov/pubmed/33800731 http://dx.doi.org/10.3390/molecules26051423 |
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author | Colobbio, Maximiliano Pandolfi, Enrique Schapiro, Valeria |
author_facet | Colobbio, Maximiliano Pandolfi, Enrique Schapiro, Valeria |
author_sort | Colobbio, Maximiliano |
collection | PubMed |
description | The preparation of a new non-natural gabosine is reported, in which the chirality is transferred from the toluene’s biotransformed metabolite (1R,2S)-3-methylcyclohexa-3.5-diene-1,2-diol. Further chemical transformations to introduce additional functionality and chirality to the molecule were also accomplished. |
format | Online Article Text |
id | pubmed-7961443 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79614432021-03-17 Enantioselective Synthesis of a New Non-Natural Gabosine Colobbio, Maximiliano Pandolfi, Enrique Schapiro, Valeria Molecules Article The preparation of a new non-natural gabosine is reported, in which the chirality is transferred from the toluene’s biotransformed metabolite (1R,2S)-3-methylcyclohexa-3.5-diene-1,2-diol. Further chemical transformations to introduce additional functionality and chirality to the molecule were also accomplished. MDPI 2021-03-06 /pmc/articles/PMC7961443/ /pubmed/33800731 http://dx.doi.org/10.3390/molecules26051423 Text en © 2021 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Colobbio, Maximiliano Pandolfi, Enrique Schapiro, Valeria Enantioselective Synthesis of a New Non-Natural Gabosine |
title | Enantioselective Synthesis of a New Non-Natural Gabosine |
title_full | Enantioselective Synthesis of a New Non-Natural Gabosine |
title_fullStr | Enantioselective Synthesis of a New Non-Natural Gabosine |
title_full_unstemmed | Enantioselective Synthesis of a New Non-Natural Gabosine |
title_short | Enantioselective Synthesis of a New Non-Natural Gabosine |
title_sort | enantioselective synthesis of a new non-natural gabosine |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7961443/ https://www.ncbi.nlm.nih.gov/pubmed/33800731 http://dx.doi.org/10.3390/molecules26051423 |
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