Total Synthesis of the Prenylated Indole Alkaloid (±)-Notoamide N via an Electrochemically Mediated Vilsmeier–Haack Formylation of a Chlorinated Indole
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| Format: | Article |
| Language: | English |
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Georg Thieme Verlag KG
2025-01-01
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| Series: | SynOpen |
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| Online Access: | http://www.thieme-connect.de/DOI/DOI?10.1055/s-0043-1773504 |
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| author | Zhongnan Xu Xin-Ting Liang Jian-Guo Song Lorenzo V. White Martin G. Banwell Shen Tan |
| author_facet | Zhongnan Xu Xin-Ting Liang Jian-Guo Song Lorenzo V. White Martin G. Banwell Shen Tan |
| author_sort | Zhongnan Xu |
| collection | DOAJ |
| format | Article |
| id | doaj-art-96494e3d67b242e3949e56ba089b08e9 |
| institution | Kabale University |
| issn | 2509-9396 |
| language | English |
| publishDate | 2025-01-01 |
| publisher | Georg Thieme Verlag KG |
| record_format | Article |
| series | SynOpen |
| spelling | doaj-art-96494e3d67b242e3949e56ba089b08e92025-01-02T23:51:04ZengGeorg Thieme Verlag KGSynOpen2509-93962025-01-0109011910.1055/s-0043-1773504Total Synthesis of the Prenylated Indole Alkaloid (±)-Notoamide N via an Electrochemically Mediated Vilsmeier–Haack Formylation of a Chlorinated IndoleZhongnan Xu0Xin-Ting Liang1Jian-Guo Song2Lorenzo V. White3Martin G. Banwell4https://orcid.org/0000-0002-0582-475XShen Tan5Institute for Advanced and Applied Chemical Synthesis, College of Pharmacy, Jinan UniversityInstitute for Advanced and Applied Chemical Synthesis, College of Pharmacy, Jinan UniversityState Key Laboratory of Bioactive Molecules and Druggability Assessment, Jinan UniversityInstitute for Advanced and Applied Chemical Synthesis, College of Pharmacy, Jinan UniversityInstitute for Advanced and Applied Chemical Synthesis, College of Pharmacy, Jinan UniversityInstitute for Advanced and Applied Chemical Synthesis, College of Pharmacy, Jinan Universityhttp://www.thieme-connect.de/DOI/DOI?10.1055/s-0043-1773504aldol reactioncycloadditionelectrochemistryepoxidationrearrangementtotal synthesis |
| spellingShingle | Zhongnan Xu Xin-Ting Liang Jian-Guo Song Lorenzo V. White Martin G. Banwell Shen Tan Total Synthesis of the Prenylated Indole Alkaloid (±)-Notoamide N via an Electrochemically Mediated Vilsmeier–Haack Formylation of a Chlorinated Indole SynOpen aldol reaction cycloaddition electrochemistry epoxidation rearrangement total synthesis |
| title | Total Synthesis of the Prenylated Indole Alkaloid (±)-Notoamide N via an Electrochemically Mediated Vilsmeier–Haack Formylation of a Chlorinated Indole |
| title_full | Total Synthesis of the Prenylated Indole Alkaloid (±)-Notoamide N via an Electrochemically Mediated Vilsmeier–Haack Formylation of a Chlorinated Indole |
| title_fullStr | Total Synthesis of the Prenylated Indole Alkaloid (±)-Notoamide N via an Electrochemically Mediated Vilsmeier–Haack Formylation of a Chlorinated Indole |
| title_full_unstemmed | Total Synthesis of the Prenylated Indole Alkaloid (±)-Notoamide N via an Electrochemically Mediated Vilsmeier–Haack Formylation of a Chlorinated Indole |
| title_short | Total Synthesis of the Prenylated Indole Alkaloid (±)-Notoamide N via an Electrochemically Mediated Vilsmeier–Haack Formylation of a Chlorinated Indole |
| title_sort | total synthesis of the prenylated indole alkaloid notoamide n via an electrochemically mediated vilsmeier haack formylation of a chlorinated indole |
| topic | aldol reaction cycloaddition electrochemistry epoxidation rearrangement total synthesis |
| url | http://www.thieme-connect.de/DOI/DOI?10.1055/s-0043-1773504 |
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