Catalytic oxidative cyclisation reactions of 1,6-enynes: a critical comparison between gold and palladium
In transition-metal catalysis, similar reactivities are often described for related metals, thereby resulting in the formation of similar/identical products. However, only in rare cases can similar/identical product be obtained by using non-related metals. Amongst these reactions is the oxidative cy...
Saved in:
| Main Authors: | , |
|---|---|
| Format: | Article (Journal) |
| Language: | English |
| Published: |
2013
|
| In: |
Israel journal of chemistry
Year: 2013, Volume: 53, Issue: 11/12, Pages: 883-891 |
| ISSN: | 1869-5868 |
| DOI: | https://doi.org/10.1002/ijch.201300072 |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/https://doi.org/10.1002/ijch.201300072 Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/ijch.201300072 |
| Author Notes: | Laura Nunes dos Santos Comprido and A. Stephen K. Hashmi |
| Summary: | In transition-metal catalysis, similar reactivities are often described for related metals, thereby resulting in the formation of similar/identical products. However, only in rare cases can similar/identical product be obtained by using non-related metals. Amongst these reactions is the oxidative cyclisation of 1,6-enynes by using palladium or gold. Similarities and differences will be discussed with a special focus on the diastereo- and enantioselective course of the reaction. |
|---|---|
| Item Description: | Gesehen am 11.05.2021 |
| Physical Description: | Online Resource |
| ISSN: | 1869-5868 |
| DOI: | https://doi.org/10.1002/ijch.201300072 |