ChemInform Abstract: Improved One-Pot Synthesis of 1-Aryl-3-trifluoroacetyl-1H-pyrroles under Swern Oxidation
Reactions of dihydrofuran (I) with aromatic amines produces enamino alcohols, which are directly submitted to Swern oxidation.
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| Veröffentlicht in: | ChemInform 2013-03, Vol.44 (13), p.no-no |
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| container_title | ChemInform |
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| creator | Zanatta, Nilo Aquino, Estefania da C. da Silva, Fabio M. Bonacorso, Helio G. Martins, Marcos A. P. |
| description | Reactions of dihydrofuran (I) with aromatic amines produces enamino alcohols, which are directly submitted to Swern oxidation. |
| doi_str_mv | 10.1002/chin.201313089 |
| format | Article |
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| ispartof | ChemInform, 2013-03, Vol.44 (13), p.no-no |
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| language | eng |
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| source | Wiley Online Library Journals Frontfile Complete |
| subjects | amination amination, N‐alkylation, N‐arylation dehydrogenation N-alkylation N-arylation Oxidation oxidation, dehydrogenation pyrrole derivatives |
| title | ChemInform Abstract: Improved One-Pot Synthesis of 1-Aryl-3-trifluoroacetyl-1H-pyrroles under Swern Oxidation |
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