том 49 издание 35 страницы 3700

Metal-free, highly efficient organocatalytic amination of benzylic C–H bonds

Тип публикацииJournal Article
Дата публикации2013-03-15
scimago Q1
wos Q2
БС1
SJR1.037
CiteScore7.4
Impact factor4.2
ISSN13597345, 1364548X
Materials Chemistry
Metals and Alloys
Surfaces, Coatings and Films
General Chemistry
Ceramics and Composites
Electronic, Optical and Magnetic Materials
Catalysis
Краткое описание
A new synthetic approach toward direct C-N bond formation through sp(3) C-H activation has been developed under metal-free conditions. Both primary and secondary benzylic C-H substrates could react smoothly with various amines to give only mono-amination products with good to excellent yields.
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ГОСТ |
Цитировать
Xue Q. et al. Metal-free, highly efficient organocatalytic amination of benzylic C–H bonds // Chemical Communications. 2013. Vol. 49. No. 35. p. 3700.
ГОСТ со всеми авторами (до 50) Скопировать
Xue Q., Xie J., Li H., Cheng Y., Zhu C. Metal-free, highly efficient organocatalytic amination of benzylic C–H bonds // Chemical Communications. 2013. Vol. 49. No. 35. p. 3700.
RIS |
Цитировать
TY - JOUR
DO - 10.1039/c3cc41558a
UR - https://doi.org/10.1039/c3cc41558a
TI - Metal-free, highly efficient organocatalytic amination of benzylic C–H bonds
T2 - Chemical Communications
AU - Xue, Qicai
AU - Xie, Jin
AU - Li, Huamin
AU - Cheng, Yixiang
AU - Zhu, Chengjian
PY - 2013
DA - 2013/03/15
PB - Royal Society of Chemistry (RSC)
SP - 3700
IS - 35
VL - 49
PMID - 23536004
SN - 1359-7345
SN - 1364-548X
ER -
BibTex |
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BibTex (до 50 авторов) Скопировать
@article{2013_Xue,
author = {Qicai Xue and Jin Xie and Huamin Li and Yixiang Cheng and Chengjian Zhu},
title = {Metal-free, highly efficient organocatalytic amination of benzylic C–H bonds},
journal = {Chemical Communications},
year = {2013},
volume = {49},
publisher = {Royal Society of Chemistry (RSC)},
month = {mar},
url = {https://doi.org/10.1039/c3cc41558a},
number = {35},
pages = {3700},
doi = {10.1039/c3cc41558a}
}
MLA
Цитировать
Xue, Qicai, et al. “Metal-free, highly efficient organocatalytic amination of benzylic C–H bonds.” Chemical Communications, vol. 49, no. 35, Mar. 2013, p. 3700. https://doi.org/10.1039/c3cc41558a.