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Enantioselective Palladium-Catalyzed Decarboxylative Dearomative Asymmetric Allylic Alkylation of Benzofurans: Diversity-Oriented Synthesis of Flavaglines
| Content Provider | Scilit |
|---|---|
| Author | Lu ∗, Hai-Hua Cao, Meng-Yue |
| Copyright Year | 2021 |
| Description | With the introduction of new Trost-type bisphosphine ligands bearing a chiral cycloalkane framework, the highly efficient and enantioselective palladium-catalyzed decarboxylative dearomative asymmetric allylic alkylation (AAA) of benzofurans was achieved. This enabled a diversity-oriented synthesis (DOS) of previously unreachable flavaglines, which features two diversification stages. A new avenue for developing flavagline-based drugs was thus established.1 Introduction2 The Dearomative Asymmetric Allylic Alkylation of Benzofurans3 Synthesis of Flavaglines4 Conclusion and Outlook |
| Related Links | http://www.thieme-connect.de/products/ejournals/pdf/10.1055/a-1650-4266.pdf |
| Ending Page | 1986 |
| Page Count | 6 |
| Starting Page | 1981 |
| ISSN | 09365214 |
| e-ISSN | 14372096 |
| DOI | 10.1055/a-1650-4266 |
| Journal | Synlett |
| Issue Number | 20 |
| Volume Number | 32 |
| Language | English |
| Publisher | Georg Thieme Verlag KG |
| Publisher Date | 2021-09-21 |
| Access Restriction | Open |
| Subject Keyword | Journal: Synlett Palladium Catalysis Dearomative Asymmetric Allylic Alkylation (aaa) Total Synthesis Diversity-oriented Synthesis (dos) N-heterocyclic Carbene (nhc) Catalysis Benzoin Condensation |
| Content Type | Text |
| Resource Type | Article |
| Subject | Organic Chemistry |