Gold catalysis: non-spirocyclic intermediates in the conversion of furanynes by the formal insertion of an alkyne into an aryl-alkyl CC single bond
It takes al-kynes: The formation of furyl-substituted heterocycles from furanynes with donor groups on the furan-alkyne tether and mechanistic control experiments indicate the involvement of open-chained carbenium ions in the overall insertion of an alkyne into a CC bond, rather than the usual spir...
Saved in:
| Main Authors: | , , , , |
|---|---|
| Format: | Article (Journal) |
| Language: | English |
| Published: |
16 July 2012
|
| In: |
Chemistry - a European journal
Year: 2012, Volume: 18, Issue: 34, Pages: 10480-10486 |
| ISSN: | 1521-3765 |
| DOI: | 10.1002/chem.201200306 |
| Online Access: | Verlag, Volltext: http://dx.doi.org/10.1002/chem.201200306 Verlag, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.201200306 |
| Author Notes: | A. Stephen K. Hashmi, Tobias Häffner, Weibo Yang, Sreekumar Pankajakshan, Sascha Schäfer, Lara Schultes, Frank Rominger, and Wolfgang Frey |
| Summary: | It takes al-kynes: The formation of furyl-substituted heterocycles from furanynes with donor groups on the furan-alkyne tether and mechanistic control experiments indicate the involvement of open-chained carbenium ions in the overall insertion of an alkyne into a CC bond, rather than the usual spirocyclic intermediates (see scheme). |
|---|---|
| Item Description: | Gesehen am 06.09.2018 |
| Physical Description: | Online Resource |
| ISSN: | 1521-3765 |
| DOI: | 10.1002/chem.201200306 |