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NHC-catalyzed cleavage of vicinal diketones and triketones followed by insertion of enones and ynones
Thiazolium carbene-catalyzed reactions of 1,2-diketones and 1,2,3-triketones with enones and ynones have been investigated. The diketones gave α,β-double acylation products via unique Breslow intermediates isolable as acid salts, whereas the triketones formed stable adducts with the NHC instead of t...
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| Published in: | Beilstein J Org Chem |
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| Main Authors: | , , , , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
Beilstein-Institut
2017
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5588593/ https://ncbi.nlm.nih.gov/pubmed/28904625 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3762/bjoc.13.176 |
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