| Item type |
学術雑誌論文 / Journal Article(1) |
| 公開日 |
2017-03-24 |
| タイトル |
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タイトル |
Tailor-Made Synthesis of N,N,2,6-Tetrasubstituted 4-Nitroanilines by Three-Component Ring Transformation of Dinitropyridone |
| 言語 |
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言語 |
eng |
| 資源タイプ |
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資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
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資源タイプ |
journal article |
| 著者 |
Le, Song Thi
Asahara, Haruyasu
Nishiwaki, Nagatoshi
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| 抄録 |
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内容記述タイプ |
Abstract |
|
内容記述 |
The ring transformation of dinitropyridone afforded various kinds of 2,6-disubstituted-4-nitroanilines upon treatment with aliphatic ketones in the presence of ammonium acetate as a nitrogen source, wherein dinitropyridone behaved as the synthetic equivalent of unstable nitromalonaldehyde. The benzene ring, as well as the amino group of the nitroaniline framework, was easily modified by only changing a ketone and the nitrogen source, which afforded N,N,2,6-tetrasubstituted 4-nitroanilines in good to excellent yields. |
| 書誌情報 |
European Journal of Organic Chemistry
巻 2015,
号 6,
p. 1203-1206,
発行日 2015-02
|
| ISSN |
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収録物識別子タイプ |
ISSN |
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収録物識別子 |
1099-0690 |
| DOI |
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|
関連タイプ |
isVersionOf |
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識別子タイプ |
DOI |
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|
関連識別子 |
10.1002/ejoc.201403652 |
| 権利 |
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|
権利情報 |
This is the accepted version of the following article: European Journal of Organic Chemistry, 2015(6), 1203-1206, 2015-02, which has been published in final form at http://dx.doi.org/10.1002/ejoc.201403652. This article may be used for non-commercial purposes in accordance with the Wiley Self-Archiving Policy [olabout.wiley.com/WileyCDA/Section/id-820227.html]. |
| 著者版フラグ |
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出版タイプ |
AM |
|
出版タイプResource |
http://purl.org/coar/version/c_ab4af688f83e57aa |
| 出版者 |
|
|
出版者 |
WILEY-VCH Verlag GmbH |
28-44.pdf (492.2 kB)
