First Ritter-type reaction of alkylbenzenes using N-hydroxyphthalimide as a key catalyst
Тип публикации: Journal Article
Дата публикации: 2002-02-11
SCImago Q1
WOS Q2
БС1
SJR: 0.907
CiteScore: 7.2
Impact factor: 4.3
ISSN: 13597345, 1364548X
PubMed ID:
12120568
Materials Chemistry
Metals and Alloys
Surfaces, Coatings and Films
General Chemistry
Ceramics and Composites
Electronic, Optical and Magnetic Materials
Catalysis
Краткое описание
The first Ritter-type reaction of alkylbenzenes with nitriles has been successfully achieved by the use of N-hydroxyphthalimide (NHPI) as a key catalyst. Thus, treatment of ethylbenzene with ammonium hexanitratocerate(IV) (CAN) in the presence of a catalytic amount of NHPI in EtCN under argon produced the corresponding amide in good selectivity.
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Всего цитирований:
63
Цитирований c 2025:
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(11.11%)
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ГОСТ
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Sakaguchi S., Hirabayashi T., Ishii Y. First Ritter-type reaction of alkylbenzenes using N-hydroxyphthalimide as a key catalyst // Chemical Communications. 2002. Vol. 5. pp. 516-517.
ГОСТ со всеми авторами (до 50)
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Sakaguchi S., Hirabayashi T., Ishii Y. First Ritter-type reaction of alkylbenzenes using N-hydroxyphthalimide as a key catalyst // Chemical Communications. 2002. Vol. 5. pp. 516-517.
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RIS
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TY - JOUR
DO - 10.1039/b110638d
UR - https://doi.org/10.1039/b110638d
TI - First Ritter-type reaction of alkylbenzenes using N-hydroxyphthalimide as a key catalyst
T2 - Chemical Communications
AU - Sakaguchi, Satoshi
AU - Hirabayashi, Tomotaka
AU - Ishii, Yasutaka
PY - 2002
DA - 2002/02/11
PB - Royal Society of Chemistry (RSC)
SP - 516-517
IS - 5
PMID - 12120568
SN - 1359-7345
SN - 1364-548X
ER -
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BibTex (до 50 авторов)
Скопировать
@article{2002_Sakaguchi,
author = {Satoshi Sakaguchi and Tomotaka Hirabayashi and Yasutaka Ishii},
title = {First Ritter-type reaction of alkylbenzenes using N-hydroxyphthalimide as a key catalyst},
journal = {Chemical Communications},
year = {2002},
publisher = {Royal Society of Chemistry (RSC)},
month = {feb},
url = {https://doi.org/10.1039/b110638d},
number = {5},
pages = {516--517},
doi = {10.1039/b110638d}
}
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