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Synthesis of Cannabinoids: “In Water” and “On Water” Approaches: Influence of SDS Micelles
[Image: see text] We have proven that the biomimetic-like synthesis of cannabinoids from citral and the corresponding phenolic counterpart may well be carried out using water as a solvent. The influence of different additives such as surfactants was also analyzed. Rationalization of the reaction mod...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9087200/ https://www.ncbi.nlm.nih.gov/pubmed/33533618 http://dx.doi.org/10.1021/acs.joc.0c02698 |
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author | Quílez del Moral, José F. Ruiz Martínez, Cristina Pérez del Pulgar, Helena Martín González, Juan Eduardo Fernández, Ignacio López-Pérez, José Luis Fernández-Arteaga, Alejandro Barrero, Alejandro F. |
author_facet | Quílez del Moral, José F. Ruiz Martínez, Cristina Pérez del Pulgar, Helena Martín González, Juan Eduardo Fernández, Ignacio López-Pérez, José Luis Fernández-Arteaga, Alejandro Barrero, Alejandro F. |
author_sort | Quílez del Moral, José F. |
collection | PubMed |
description | [Image: see text] We have proven that the biomimetic-like synthesis of cannabinoids from citral and the corresponding phenolic counterpart may well be carried out using water as a solvent. The influence of different additives such as surfactants was also analyzed. Rationalization of the reaction mode and regiochemistry of the processes were provided in terms of “on water” and “in water” reactions. The same reactions were conducted in organic media using Ga(III) salts as catalysts. Worthy of being underlined, an unprecedented formal [2+2+2] process was found to occur between two citral molecules and the corresponding phenolic species in both aqueous and organic environments. Computational studies were performed in order to gain a comprehensive mechanistic and energetic understanding of the different steps of this singular process. Finally, the influence of SDS micelles in the chemical behavior of olivetol and citral was also pursued using PGSE diffusion and NOESY NMR studies. These data permitted to tentatively propose the existence of a mixed micelle between olivetol and SDS assemblies. |
format | Online Article Text |
id | pubmed-9087200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-90872002022-05-10 Synthesis of Cannabinoids: “In Water” and “On Water” Approaches: Influence of SDS Micelles Quílez del Moral, José F. Ruiz Martínez, Cristina Pérez del Pulgar, Helena Martín González, Juan Eduardo Fernández, Ignacio López-Pérez, José Luis Fernández-Arteaga, Alejandro Barrero, Alejandro F. J Org Chem [Image: see text] We have proven that the biomimetic-like synthesis of cannabinoids from citral and the corresponding phenolic counterpart may well be carried out using water as a solvent. The influence of different additives such as surfactants was also analyzed. Rationalization of the reaction mode and regiochemistry of the processes were provided in terms of “on water” and “in water” reactions. The same reactions were conducted in organic media using Ga(III) salts as catalysts. Worthy of being underlined, an unprecedented formal [2+2+2] process was found to occur between two citral molecules and the corresponding phenolic species in both aqueous and organic environments. Computational studies were performed in order to gain a comprehensive mechanistic and energetic understanding of the different steps of this singular process. Finally, the influence of SDS micelles in the chemical behavior of olivetol and citral was also pursued using PGSE diffusion and NOESY NMR studies. These data permitted to tentatively propose the existence of a mixed micelle between olivetol and SDS assemblies. American Chemical Society 2021-02-03 2021-02-19 /pmc/articles/PMC9087200/ /pubmed/33533618 http://dx.doi.org/10.1021/acs.joc.0c02698 Text en © 2021 American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Quílez del Moral, José F. Ruiz Martínez, Cristina Pérez del Pulgar, Helena Martín González, Juan Eduardo Fernández, Ignacio López-Pérez, José Luis Fernández-Arteaga, Alejandro Barrero, Alejandro F. Synthesis of Cannabinoids: “In Water” and “On Water” Approaches: Influence of SDS Micelles |
title | Synthesis of Cannabinoids:
“In Water”
and “On Water” Approaches: Influence of SDS Micelles |
title_full | Synthesis of Cannabinoids:
“In Water”
and “On Water” Approaches: Influence of SDS Micelles |
title_fullStr | Synthesis of Cannabinoids:
“In Water”
and “On Water” Approaches: Influence of SDS Micelles |
title_full_unstemmed | Synthesis of Cannabinoids:
“In Water”
and “On Water” Approaches: Influence of SDS Micelles |
title_short | Synthesis of Cannabinoids:
“In Water”
and “On Water” Approaches: Influence of SDS Micelles |
title_sort | synthesis of cannabinoids:
“in water”
and “on water” approaches: influence of sds micelles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9087200/ https://www.ncbi.nlm.nih.gov/pubmed/33533618 http://dx.doi.org/10.1021/acs.joc.0c02698 |
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