Replacing dichloroethane as a solvent for rhodium-catalysed intermolecular alkyne hydroacylation reactions: the utility of propylene carbonate
Propylene carbonate is an excellent solvent for rhodium-catalysed intermolecular alkyne hydroacylation reactions, allowing a variety of β-S-aldehydes and alkynes to be combined in high yields, to deliver enone products. The effective use of propylene carbonate removes the need to employ dichloroetha...
| Glavni autori: | , , , , |
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| Format: | Journal article |
| Jezik: | English |
| Izdano: |
2011
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| _version_ | 1826296936495316992 |
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| author | Lenden, P Ylioja, P Gonzalez-Rodriguez, C Entwistle, D Willis, M |
| author_facet | Lenden, P Ylioja, P Gonzalez-Rodriguez, C Entwistle, D Willis, M |
| author_sort | Lenden, P |
| collection | OXFORD |
| description | Propylene carbonate is an excellent solvent for rhodium-catalysed intermolecular alkyne hydroacylation reactions, allowing a variety of β-S-aldehydes and alkynes to be combined in high yields, to deliver enone products. The effective use of propylene carbonate removes the need to employ dichloroethane as solvent. © 2011 The Royal Society of Chemistry. |
| first_indexed | 2024-03-07T04:23:59Z |
| format | Journal article |
| id | oxford-uuid:cbff132d-81e4-408f-ab6f-0e60233f2ac5 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T04:23:59Z |
| publishDate | 2011 |
| record_format | dspace |
| spelling | oxford-uuid:cbff132d-81e4-408f-ab6f-0e60233f2ac52022-03-27T07:18:40ZReplacing dichloroethane as a solvent for rhodium-catalysed intermolecular alkyne hydroacylation reactions: the utility of propylene carbonateJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:cbff132d-81e4-408f-ab6f-0e60233f2ac5EnglishSymplectic Elements at Oxford2011Lenden, PYlioja, PGonzalez-Rodriguez, CEntwistle, DWillis, MPropylene carbonate is an excellent solvent for rhodium-catalysed intermolecular alkyne hydroacylation reactions, allowing a variety of β-S-aldehydes and alkynes to be combined in high yields, to deliver enone products. The effective use of propylene carbonate removes the need to employ dichloroethane as solvent. © 2011 The Royal Society of Chemistry. |
| spellingShingle | Lenden, P Ylioja, P Gonzalez-Rodriguez, C Entwistle, D Willis, M Replacing dichloroethane as a solvent for rhodium-catalysed intermolecular alkyne hydroacylation reactions: the utility of propylene carbonate |
| title | Replacing dichloroethane as a solvent for rhodium-catalysed intermolecular alkyne hydroacylation reactions: the utility of propylene carbonate |
| title_full | Replacing dichloroethane as a solvent for rhodium-catalysed intermolecular alkyne hydroacylation reactions: the utility of propylene carbonate |
| title_fullStr | Replacing dichloroethane as a solvent for rhodium-catalysed intermolecular alkyne hydroacylation reactions: the utility of propylene carbonate |
| title_full_unstemmed | Replacing dichloroethane as a solvent for rhodium-catalysed intermolecular alkyne hydroacylation reactions: the utility of propylene carbonate |
| title_short | Replacing dichloroethane as a solvent for rhodium-catalysed intermolecular alkyne hydroacylation reactions: the utility of propylene carbonate |
| title_sort | replacing dichloroethane as a solvent for rhodium catalysed intermolecular alkyne hydroacylation reactions the utility of propylene carbonate |
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