Silver-catalyzed carboxylative cyclization of primary propargyl alcohols with CO2
By using silver complexes with bulky ligands such as DavePhos or N-heterocyclic carbenes, propargylic alcohols are smoothly converted with CO2 into a unique class of unexplored cyclic alkylidene carbonates. These systems, for the first time, also achieve the direct carboxylative cyclization of prima...
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| Hauptverfasser: | , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
February 20, 2019
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| In: |
Organic letters
Year: 2019, Jahrgang: 21, Heft: 5, Pages: 1422-1425 |
| ISSN: | 1523-7052 |
| DOI: | 10.1021/acs.orglett.9b00156 |
| Online-Zugang: | Verlag, Volltext: https://doi.org/10.1021/acs.orglett.9b00156 |
| Verfasserangaben: | Saumya Dabral, Bilguun Bayarmagnai, Marko Hermsen, Jasmin Schießl, Verena Mormul, A. Stephen K. Hashmi, and Thomas Schaub |
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| 246 | 3 | 3 | |a Silver-catalyzed carboxylative cyclization of primary propargyl alcohols with carbon dioxide |
| 246 | 3 | 3 | |a Silver-catalyzed carboxylative cyclization of primary propargyl alcohols with CO 2 |
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| 520 | |a By using silver complexes with bulky ligands such as DavePhos or N-heterocyclic carbenes, propargylic alcohols are smoothly converted with CO2 into a unique class of unexplored cyclic alkylidene carbonates. These systems, for the first time, also achieve the direct carboxylative cyclization of primary propargylic alcohols. The silver-DavePhos catalyst is further applied for the bis-carboxylative cyclization of primary propargyl derivatives, thereby providing an effective route to a series of previously inaccessible and industrially relevant α-alkylidene cyclic carbonates. | ||
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