Springer Nature
Chemistry of Natural Compounds
,  том 50 ,  издание 4 ,  страницы 648-651

New Optically Active CN-Palladacycles Based on 2α-Hydroxypinan-3-One and Camphor Derivatives

Тип публикации: Journal Article
Дата публикации: 2014-09-11
Springer Nature
scimago Q3
wos Q4
БС3
SJR: 0.296
CiteScore: 1.3
Impact factor: 0.9
ISSN: 00093130, 15738388
General Chemistry
General Biochemistry, Genetics and Molecular Biology
Plant Science
Краткое описание
The ligand (–)-2α-hydroxypinan-3-one diphenylmethylimine was synthesized and studied. New dinuclear CN-palladacycles and their mononuclear triphenylphosphine derivatives were obtained. It was shown that ortho-palladation of terpene diphenylmethylimines produced pure stereoisomers.
Найдено 
Найдено 

Топ-30

Журналы

1
2
3
Russian Chemical Bulletin
Russian Chemical Bulletin, 3, 33.33%
Russian Chemical Bulletin
3 публикации, 33.33%
Russian Chemical Reviews
Russian Chemical Reviews, 2, 22.22%
Russian Chemical Reviews
2 публикации, 22.22%
Antibiotics
Antibiotics, 1, 11.11%
Antibiotics
1 публикация, 11.11%
Inorganica Chimica Acta
Inorganica Chimica Acta, 1, 11.11%
Inorganica Chimica Acta
1 публикация, 11.11%
Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya
Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya, 1, 11.11%
Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya
1 публикация, 11.11%
Координационная химия
Координационная химия, 1, 11.11%
Координационная химия
1 публикация, 11.11%
1
2
3

Издатели

1
2
3
Springer Nature
Springer Nature, 3, 33.33%
Springer Nature
3 публикации, 33.33%
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii, 2, 22.22%
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
2 публикации, 22.22%
Pleiades Publishing
Pleiades Publishing, 2, 22.22%
Pleiades Publishing
2 публикации, 22.22%
MDPI
MDPI, 1, 11.11%
MDPI
1 публикация, 11.11%
Elsevier
Elsevier, 1, 11.11%
Elsevier
1 публикация, 11.11%
1
2
3
  • Мы не учитываем публикации, у которых нет DOI.
  • Статистика публикаций обновляется еженедельно.

Вы ученый?

Создайте профиль, чтобы получать персональные рекомендации коллег, конференций и новых статей.
Метрики
9
Поделиться
Цитировать
ГОСТ |
Цитировать
ГОСТ Скопировать
Gur′eva Ya. A. et al. New Optically Active CN-Palladacycles Based on 2α-Hydroxypinan-3-One and Camphor Derivatives // Chemistry of Natural Compounds. 2014. Vol. 50. No. 4. pp. 648-651.
ГОСТ со всеми авторами (до 50) Скопировать
Gur′eva Ya. A., Zalevskaya O. A., Alekseev I. N., Frolova L. L., Slepukhin P. A., Kuchin A. V. New Optically Active CN-Palladacycles Based on 2α-Hydroxypinan-3-One and Camphor Derivatives // Chemistry of Natural Compounds. 2014. Vol. 50. No. 4. pp. 648-651.
RIS |
Цитировать
RIS Скопировать
TY - JOUR
DO - 10.1007/s10600-014-1044-3
UR - https://doi.org/10.1007/s10600-014-1044-3
TI - New Optically Active CN-Palladacycles Based on 2α-Hydroxypinan-3-One and Camphor Derivatives
T2 - Chemistry of Natural Compounds
AU - Gur′eva, Ya A
AU - Zalevskaya, O A
AU - Alekseev, I N
AU - Frolova, L L
AU - Slepukhin, P A
AU - Kuchin, A. V.
PY - 2014
DA - 2014/09/11
PB - Springer Nature
SP - 648-651
IS - 4
VL - 50
SN - 0009-3130
SN - 1573-8388
ER -
BibTex |
Цитировать
BibTex (до 50 авторов) Скопировать
@article{2014_Gur′eva,
author = {Ya A Gur′eva and O A Zalevskaya and I N Alekseev and L L Frolova and P A Slepukhin and A. V. Kuchin},
title = {New Optically Active CN-Palladacycles Based on 2α-Hydroxypinan-3-One and Camphor Derivatives},
journal = {Chemistry of Natural Compounds},
year = {2014},
volume = {50},
publisher = {Springer Nature},
month = {sep},
url = {https://doi.org/10.1007/s10600-014-1044-3},
number = {4},
pages = {648--651},
doi = {10.1007/s10600-014-1044-3}
}
MLA
Цитировать
MLA Скопировать
Gur′eva, Ya. A., et al. “New Optically Active CN-Palladacycles Based on 2α-Hydroxypinan-3-One and Camphor Derivatives.” Chemistry of Natural Compounds, vol. 50, no. 4, Sep. 2014, pp. 648-651. https://doi.org/10.1007/s10600-014-1044-3.