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A tandem Mannich addition–palladium catalyzed ring-closing route toward 4-substituted-3(2H)-furanones
A facile route towards highly functionalized 3(2H)-furanones via a sequential Mannich addition–palladium catalyzed ring closing has been elaborated. The reaction of 4-chloroacetoacetate esters with imines derived from aliphatic and aromatic aldehydes under palladium catalysis afforded 4-substituted...
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| Hlavní autoři: | , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Beilstein-Institut
2014
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4077403/ https://ncbi.nlm.nih.gov/pubmed/24991301 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3762/bjoc.10.150 |
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