Synthesis of Cannabinoids: “In Water” and “On Water” Approaches: Influence of SDS Micelles
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 regiochemist...
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Veröffentlicht in: | Journal of organic chemistry 2021-02, Vol.86 (4), p.3344-3355 |
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container_title | Journal of organic chemistry |
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creator | 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. |
description | 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. |
doi_str_mv | 10.1021/acs.joc.0c02698 |
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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. 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Org. Chem</addtitle><description>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. 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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.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>33533618</pmid><doi>10.1021/acs.joc.0c02698</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-4806-6693</orcidid><orcidid>https://orcid.org/0000-0001-8355-580X</orcidid><orcidid>https://orcid.org/0000-0002-3728-7602</orcidid><orcidid>https://orcid.org/0000-0002-5407-7877</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Cannabinoids Micelles Solvents Surface-Active Agents Water |
title | Synthesis of Cannabinoids: “In Water” and “On Water” Approaches: Influence of SDS Micelles |
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