A bifunctional spiro-type organocatalyst with high enantiocontrol: application to the aza-Morita–Baylis–Hillman reactions
Тип публикации: Journal Article
Дата публикации: 2011-07-19
SCImago Q1
WOS Q2
БС1
SJR: 0.907
CiteScore: 7.2
Impact factor: 4.3
ISSN: 13597345, 1364548X
PubMed ID:
21769347
Materials Chemistry
Metals and Alloys
Surfaces, Coatings and Films
General Chemistry
Ceramics and Composites
Electronic, Optical and Magnetic Materials
Catalysis
Краткое описание
A unique spiro-type Brønsted acid-Lewis base organocatalyst has been developed. The new bifunctional organocatalyst promoted aza-Morita-Baylis-Hillman reactions to yield adducts with up to 98% ee.
Найдено
Ничего не найдено, попробуйте изменить настройки фильтра.
Для доступа к списку цитирований публикации необходимо авторизоваться.
Топ-30
Журналы
|
1
2
3
4
|
|
|
Angewandte Chemie
4 публикации, 7.41%
|
|
|
Angewandte Chemie - International Edition
4 публикации, 7.41%
|
|
|
Chemistry - A European Journal
3 публикации, 5.56%
|
|
|
European Journal of Organic Chemistry
3 публикации, 5.56%
|
|
|
Chemical Reviews
3 публикации, 5.56%
|
|
|
Tetrahedron
2 публикации, 3.7%
|
|
|
Tetrahedron Asymmetry
2 публикации, 3.7%
|
|
|
Journal of the American Chemical Society
2 публикации, 3.7%
|
|
|
ACS Catalysis
2 публикации, 3.7%
|
|
|
Journal of Organic Chemistry
2 публикации, 3.7%
|
|
|
Organic Letters
2 публикации, 3.7%
|
|
|
Organic and Biomolecular Chemistry
2 публикации, 3.7%
|
|
|
Chemical Communications
2 публикации, 3.7%
|
|
|
Organic Chemistry Frontiers
2 публикации, 3.7%
|
|
|
Organic Reaction Mechanisms
2 публикации, 3.7%
|
|
|
Russian Chemical Bulletin
2 публикации, 3.7%
|
|
|
Chemical and Pharmaceutical Bulletin
1 публикация, 1.85%
|
|
|
Crystals
1 публикация, 1.85%
|
|
|
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
1 публикация, 1.85%
|
|
|
Catalysis Letters
1 публикация, 1.85%
|
|
|
Tetrahedron Letters
1 публикация, 1.85%
|
|
|
Advanced Synthesis and Catalysis
1 публикация, 1.85%
|
|
|
ChemInform
1 публикация, 1.85%
|
|
|
Organometallics
1 публикация, 1.85%
|
|
|
RSC Advances
1 публикация, 1.85%
|
|
|
Russian Journal of General Chemistry
1 публикация, 1.85%
|
|
|
Green Chemistry
1 публикация, 1.85%
|
|
|
1
2
3
4
|
Издатели
|
5
10
15
20
25
|
|
|
Wiley
21 публикация, 38.89%
|
|
|
American Chemical Society (ACS)
12 публикаций, 22.22%
|
|
|
Royal Society of Chemistry (RSC)
8 публикаций, 14.81%
|
|
|
Elsevier
5 публикаций, 9.26%
|
|
|
Springer Nature
3 публикации, 5.56%
|
|
|
Pharmaceutical Society of Japan
1 публикация, 1.85%
|
|
|
MDPI
1 публикация, 1.85%
|
|
|
The Society of Synthetic Organic Chemistry, Japan
1 публикация, 1.85%
|
|
|
Pleiades Publishing
1 публикация, 1.85%
|
|
|
5
10
15
20
25
|
- 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.
Войти с ORCID
Метрики
54
Всего цитирований:
54
Цитирований c 2025:
2
(3.7%)
Цитировать
ГОСТ |
RIS |
BibTex |
MLA
Цитировать
ГОСТ
Скопировать
Takizawa S. et al. A bifunctional spiro-type organocatalyst with high enantiocontrol: application to the aza-Morita–Baylis–Hillman reactions // Chemical Communications. 2011. Vol. 47. No. 32. p. 9227.
ГОСТ со всеми авторами (до 50)
Скопировать
Takizawa S., Kiriyama K., Ieki K., Sasai H. A bifunctional spiro-type organocatalyst with high enantiocontrol: application to the aza-Morita–Baylis–Hillman reactions // Chemical Communications. 2011. Vol. 47. No. 32. p. 9227.
Цитировать
RIS
Скопировать
TY - JOUR
DO - 10.1039/c1cc12784e
UR - https://doi.org/10.1039/c1cc12784e
TI - A bifunctional spiro-type organocatalyst with high enantiocontrol: application to the aza-Morita–Baylis–Hillman reactions
T2 - Chemical Communications
AU - Takizawa, Shinobu
AU - Kiriyama, Kimiko
AU - Ieki, Kenta
AU - Sasai, Hiroaki
PY - 2011
DA - 2011/07/19
PB - Royal Society of Chemistry (RSC)
SP - 9227
IS - 32
VL - 47
PMID - 21769347
SN - 1359-7345
SN - 1364-548X
ER -
Цитировать
BibTex (до 50 авторов)
Скопировать
@article{2011_Takizawa,
author = {Shinobu Takizawa and Kimiko Kiriyama and Kenta Ieki and Hiroaki Sasai},
title = {A bifunctional spiro-type organocatalyst with high enantiocontrol: application to the aza-Morita–Baylis–Hillman reactions},
journal = {Chemical Communications},
year = {2011},
volume = {47},
publisher = {Royal Society of Chemistry (RSC)},
month = {jul},
url = {https://doi.org/10.1039/c1cc12784e},
number = {32},
pages = {9227},
doi = {10.1039/c1cc12784e}
}
Цитировать
MLA
Скопировать
Takizawa, Shinobu, et al. “A bifunctional spiro-type organocatalyst with high enantiocontrol: application to the aza-Morita–Baylis–Hillman reactions.” Chemical Communications, vol. 47, no. 32, Jul. 2011, p. 9227. https://doi.org/10.1039/c1cc12784e.
Ошибка в публикации?