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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Bibliographic Details
Main Authors: Dabral, Saumya (Author) , Schießl, Jasmin (Author) , Hashmi, A. Stephen K. (Author)
Format: Article (Journal)
Language:English
Published: February 20, 2019
In: Organic letters
Year: 2019, Volume: 21, Issue: 5, Pages: 1422-1425
ISSN:1523-7052
DOI:10.1021/acs.orglett.9b00156
Online Access:Verlag, Volltext: https://doi.org/10.1021/acs.orglett.9b00156
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Author Notes:Saumya Dabral, Bilguun Bayarmagnai, Marko Hermsen, Jasmin Schießl, Verena Mormul, A. Stephen K. Hashmi, and Thomas Schaub
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Summary: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.
Item Description:Im Titel ist „2“ tiefgestellt
Gesehen am 09.05.2019
Physical Description:Online Resource
ISSN:1523-7052
DOI:10.1021/acs.orglett.9b00156