Conversion of Oximes to Carbonyl Compounds with 2-Nitro-4,5-dichloropyridazin-3(2H)-one
Conversion of oximes to the carbonyl compounds has been demonstrated with use of 2-nitro-4,5-dichloropyridazin-3(2H)-one (2) under microwave irradiated conditions. Fourteen aliphatic and aromatic oximes converted to their corresponding aldehydes and ketones in good to excellent yields. It is notewor...
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Veröffentlicht in: | Journal of organic chemistry 2010-01, Vol.75 (2), p.484-486 |
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container_title | Journal of organic chemistry |
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creator | Kim, Bo Ram Lee, Hyung-Geun Kim, Eun Jung Lee, Sang-Gyeong Yoon, Yong-Jin |
description | Conversion of oximes to the carbonyl compounds has been demonstrated with use of 2-nitro-4,5-dichloropyridazin-3(2H)-one (2) under microwave irradiated conditions. Fourteen aliphatic and aromatic oximes converted to their corresponding aldehydes and ketones in good to excellent yields. It is noteworthy that the reaction is conducted under neutral, mild, and eco-friendly condition. |
doi_str_mv | 10.1021/jo902356e |
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Fourteen aliphatic and aromatic oximes converted to their corresponding aldehydes and ketones in good to excellent yields. 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Org. Chem</addtitle><description>Conversion of oximes to the carbonyl compounds has been demonstrated with use of 2-nitro-4,5-dichloropyridazin-3(2H)-one (2) under microwave irradiated conditions. Fourteen aliphatic and aromatic oximes converted to their corresponding aldehydes and ketones in good to excellent yields. 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title | Conversion of Oximes to Carbonyl Compounds with 2-Nitro-4,5-dichloropyridazin-3(2H)-one |
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