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161202s2016 xx ||||| 00| ||eng c |
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|a (KEY)0384431520160000018001804594palladiumcatalyzedregioselectivec8haminationof1nap
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|a Li, Zexian
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|a Palladium-Catalyzed Regioselective C8-H Amination of 1-Naphthylamine Derivatives with Aliphatic Amines
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|c 2016
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|a Text
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|a ohne Hilfsmittel zu benutzen
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|a A simple and facile protocol for palladium-catalyzed picolinamide-directed C8-H amination of 1-naphthylamine derivatives with simple secondary aliphatic amines was developed, thereby providing a new route to 1,8-naphthalenediamine derivatives. It is noteworthy that the picolinamide moiety as a bidentate directing group may play a key role in this regioselective transformation.
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|a Sun, Suyan
|4 oth
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|a Qiao, Huijie
|4 oth
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|a Yang, Fan
|4 oth
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|a Zhu, Yu
|4 oth
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|a Kang, Jianxun
|4 oth
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|a Wu, Yusheng
|4 oth
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|a Wu, Yangjie
|4 oth
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|i Enthalten in
|t Organic letters
|d Washington, DC [u.a.] : Soc., 1999
|g 18(2016), 18, Seite 4594
|w (DE-627)253386241
|w (DE-600)1458039-1
|w (DE-576)078991811
|x 1523-7060
|7 nnns
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| 773 |
1 |
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|g volume:18
|g year:2016
|g number:18
|g pages:4594
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| 856 |
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|u http://www.ncbi.nlm.nih.gov/pubmed/27584840
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