Oxidation of 1-Amidoalkyl-2-naphthols Using (Diacetoxyiodo)benzene: Unusual Formation of 1-Arylnaphtho[1,2-d]isoxazoles
Abstract The reactions of 1-amidoalkyl-2-naphthols with (diacetoxyiodo)benzene results in the unusual formation of 1-arylnaphtho[1,2- d ]isoxazoles. This procedure demonstrates a useful application of (diacetoxyiodo)benzene for the oxidative formation of an N–O bond.
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| Veröffentlicht in: | Synthesis (Stuttgart) 2014-03, Vol.46 (6), p.752-756 |
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| container_end_page | 756 |
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| container_issue | 6 |
| container_start_page | 752 |
| container_title | Synthesis (Stuttgart) |
| container_volume | 46 |
| creator | Shelke, Amol V. Bhong, Bhagyashree Y. Karade, Nandkishor N. |
| description | Abstract
The reactions of 1-amidoalkyl-2-naphthols with (diacetoxyiodo)benzene results in the unusual formation of 1-arylnaphtho[1,2-
d
]isoxazoles. This procedure demonstrates a useful application of (diacetoxyiodo)benzene for the oxidative formation of an N–O bond. |
| doi_str_mv | 10.1055/s-0033-1338590 |
| format | Article |
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The reactions of 1-amidoalkyl-2-naphthols with (diacetoxyiodo)benzene results in the unusual formation of 1-arylnaphtho[1,2-
d
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The reactions of 1-amidoalkyl-2-naphthols with (diacetoxyiodo)benzene results in the unusual formation of 1-arylnaphtho[1,2-
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The reactions of 1-amidoalkyl-2-naphthols with (diacetoxyiodo)benzene results in the unusual formation of 1-arylnaphtho[1,2-
d
]isoxazoles. This procedure demonstrates a useful application of (diacetoxyiodo)benzene for the oxidative formation of an N–O bond.</abstract><cop>Stuttgart · New York</cop><pub>Georg Thieme Verlag</pub><doi>10.1055/s-0033-1338590</doi><tpages>5</tpages></addata></record> |
| fulltext | fulltext |
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| ispartof | Synthesis (Stuttgart), 2014-03, Vol.46 (6), p.752-756 |
| issn | 0039-7881 1437-210X |
| language | eng |
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| source | Thieme Connect Journals |
| title | Oxidation of 1-Amidoalkyl-2-naphthols Using (Diacetoxyiodo)benzene: Unusual Formation of 1-Arylnaphtho[1,2-d]isoxazoles |
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