Synthesis of Novel Aryl-Substituted Acetylenic Monoterpene Analogues by Sonogashira Coupling
The synthesis of new aryl-substituted acetylenic monoterpene derivatives was carried out by the Sonogashira reaction. The reactions proceed in the presence of PdCl<sub>2</sub>(PPh<sub>3</sub>)<sub>2</sub>, CuI and Et<sub>3</sub>N and provide aryl-subst...
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MDPI AG
2024-11-01
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| Series: | Chemistry Proceedings |
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| Online Access: | https://www.mdpi.com/2673-4583/16/1/44 |
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| author | Rinat Gubaidullin Lyudmila Parfenova |
| author_facet | Rinat Gubaidullin Lyudmila Parfenova |
| author_sort | Rinat Gubaidullin |
| collection | DOAJ |
| description | The synthesis of new aryl-substituted acetylenic monoterpene derivatives was carried out by the Sonogashira reaction. The reactions proceed in the presence of PdCl<sub>2</sub>(PPh<sub>3</sub>)<sub>2</sub>, CuI and Et<sub>3</sub>N and provide aryl-substituted acetylenic monoterpenes with an isolated yield of 70–82%. |
| format | Article |
| id | doaj-art-2a901f82aef24703a32ffd56d5e5f7a8 |
| institution | OA Journals |
| issn | 2673-4583 |
| language | English |
| publishDate | 2024-11-01 |
| publisher | MDPI AG |
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| series | Chemistry Proceedings |
| spelling | doaj-art-2a901f82aef24703a32ffd56d5e5f7a82025-08-20T02:24:25ZengMDPI AGChemistry Proceedings2673-45832024-11-011614410.3390/ecsoc-28-20124Synthesis of Novel Aryl-Substituted Acetylenic Monoterpene Analogues by Sonogashira CouplingRinat Gubaidullin0Lyudmila Parfenova1Institute of Petrochemistry and Catalysis, Ufa Federal Research Center, Russian Academy of Sciences 141 Prospekt Oktyabrya, Ufa 450075, RussiaInstitute of Petrochemistry and Catalysis, Ufa Federal Research Center, Russian Academy of Sciences 141 Prospekt Oktyabrya, Ufa 450075, RussiaThe synthesis of new aryl-substituted acetylenic monoterpene derivatives was carried out by the Sonogashira reaction. The reactions proceed in the presence of PdCl<sub>2</sub>(PPh<sub>3</sub>)<sub>2</sub>, CuI and Et<sub>3</sub>N and provide aryl-substituted acetylenic monoterpenes with an isolated yield of 70–82%.https://www.mdpi.com/2673-4583/16/1/44monoterpenescamphorcarvonealkylationreductionSonogashira reaction |
| spellingShingle | Rinat Gubaidullin Lyudmila Parfenova Synthesis of Novel Aryl-Substituted Acetylenic Monoterpene Analogues by Sonogashira Coupling Chemistry Proceedings monoterpenes camphor carvone alkylation reduction Sonogashira reaction |
| title | Synthesis of Novel Aryl-Substituted Acetylenic Monoterpene Analogues by Sonogashira Coupling |
| title_full | Synthesis of Novel Aryl-Substituted Acetylenic Monoterpene Analogues by Sonogashira Coupling |
| title_fullStr | Synthesis of Novel Aryl-Substituted Acetylenic Monoterpene Analogues by Sonogashira Coupling |
| title_full_unstemmed | Synthesis of Novel Aryl-Substituted Acetylenic Monoterpene Analogues by Sonogashira Coupling |
| title_short | Synthesis of Novel Aryl-Substituted Acetylenic Monoterpene Analogues by Sonogashira Coupling |
| title_sort | synthesis of novel aryl substituted acetylenic monoterpene analogues by sonogashira coupling |
| topic | monoterpenes camphor carvone alkylation reduction Sonogashira reaction |
| url | https://www.mdpi.com/2673-4583/16/1/44 |
| work_keys_str_mv | AT rinatgubaidullin synthesisofnovelarylsubstitutedacetylenicmonoterpeneanaloguesbysonogashiracoupling AT lyudmilaparfenova synthesisofnovelarylsubstitutedacetylenicmonoterpeneanaloguesbysonogashiracoupling |