N-Heterocyclic carbene catalysis: enantioselective formal [2+2] cycloaddition of ketenes and N-sulfinylanilines.
Тип публикации: Journal Article
Дата публикации: 2011-08-25
SCImago Q1
Tоп 10% SCImago
БС1
SJR: 5.495
CiteScore: 27.6
Impact factor: 16.9
ISSN: 14337851, 15213773
PubMed ID:
21919141
General Chemistry
Catalysis
Краткое описание
As analogues of both b-sultams and b-lactams, 3-oxo-bsultams (1,2-thiazetidin-3-one 1,1-dioxides), are a novel class of four-membered heterocycles showing interesting biological activities. However, to the best of our knowledge, there is no report for the enantioselective synthesis of these heterocycles. We envisioned that the 3-oxo-b-sultams could be easily synthesized by oxidation of the corresponding 1,2-thiazetidin3-one 1-oxides (A), which could be accessed from the [2+2] cycloaddition of ketenes with N-sulfinylamines (Scheme 1).
Найдено
Ничего не найдено, попробуйте изменить настройки фильтра.
Для доступа к списку цитирований публикации необходимо авторизоваться.
Для доступа к списку профилей, цитирующих публикацию, необходимо авторизоваться.
Топ-30
Журналы
|
2
4
6
8
10
12
|
|
|
Organic Letters
12 публикаций, 9.38%
|
|
|
Organic and Biomolecular Chemistry
9 публикаций, 7.03%
|
|
|
Angewandte Chemie - International Edition
7 публикаций, 5.47%
|
|
|
Angewandte Chemie
7 публикаций, 5.47%
|
|
|
Organic Chemistry Frontiers
5 публикаций, 3.91%
|
|
|
Chemistry - A European Journal
4 публикации, 3.13%
|
|
|
Advanced Synthesis and Catalysis
4 публикации, 3.13%
|
|
|
European Journal of Organic Chemistry
4 публикации, 3.13%
|
|
|
Asian Journal of Organic Chemistry
3 публикации, 2.34%
|
|
|
Chinese Journal of Chemistry
3 публикации, 2.34%
|
|
|
Chemical Reviews
3 публикации, 2.34%
|
|
|
Journal of Organic Chemistry
3 публикации, 2.34%
|
|
|
ACS Catalysis
3 публикации, 2.34%
|
|
|
Chemical Communications
3 публикации, 2.34%
|
|
|
RSC Advances
3 публикации, 2.34%
|
|
|
Chemical Science
3 публикации, 2.34%
|
|
|
Synthesis
3 публикации, 2.34%
|
|
|
Chinese Chemical Letters
2 публикации, 1.56%
|
|
|
Chemical Record
2 публикации, 1.56%
|
|
|
Science advances
2 публикации, 1.56%
|
|
|
Progress in Heterocyclic Chemistry
2 публикации, 1.56%
|
|
|
Nature Chemistry
2 публикации, 1.56%
|
|
|
Topics in Current Chemistry
1 публикация, 0.78%
|
|
|
Materials
1 публикация, 0.78%
|
|
|
Nature Communications
1 публикация, 0.78%
|
|
|
Communications Chemistry
1 публикация, 0.78%
|
|
|
Journal of Saudi Chemical Society
1 публикация, 0.78%
|
|
|
Materials Letters
1 публикация, 0.78%
|
|
|
Tetrahedron Asymmetry
1 публикация, 0.78%
|
|
|
2
4
6
8
10
12
|
Издатели
|
5
10
15
20
25
30
35
40
45
|
|
|
Wiley
45 публикаций, 35.16%
|
|
|
Royal Society of Chemistry (RSC)
26 публикаций, 20.31%
|
|
|
American Chemical Society (ACS)
24 публикации, 18.75%
|
|
|
Elsevier
15 публикаций, 11.72%
|
|
|
Springer Nature
7 публикаций, 5.47%
|
|
|
Georg Thieme Verlag KG
3 публикации, 2.34%
|
|
|
American Association for the Advancement of Science (AAAS)
3 публикации, 2.34%
|
|
|
MDPI
1 публикация, 0.78%
|
|
|
King Saud University
1 публикация, 0.78%
|
|
|
The Japan Institute of Heterocyclic Chemistry
1 публикация, 0.78%
|
|
|
Hindawi Limited
1 публикация, 0.78%
|
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 публикация, 0.78%
|
|
|
5
10
15
20
25
30
35
40
45
|
- 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
128
Всего цитирований:
128
Цитирований c 2025:
17
(13.28%)
Цитировать
ГОСТ |
RIS |
BibTex |
MLA
Цитировать
ГОСТ
Скопировать
Jian T. et al. N-Heterocyclic carbene catalysis: enantioselective formal [2+2] cycloaddition of ketenes and N-sulfinylanilines. // Angewandte Chemie - International Edition. 2011. Vol. 50. No. 39. pp. 9104-9107.
ГОСТ со всеми авторами (до 50)
Скопировать
Jian T., He L., Tang C., Song Ye S. N-Heterocyclic carbene catalysis: enantioselective formal [2+2] cycloaddition of ketenes and N-sulfinylanilines. // Angewandte Chemie - International Edition. 2011. Vol. 50. No. 39. pp. 9104-9107.
Цитировать
RIS
Скопировать
TY - JOUR
DO - 10.1002/anie.201102488
UR - https://doi.org/10.1002/anie.201102488
TI - N-Heterocyclic carbene catalysis: enantioselective formal [2+2] cycloaddition of ketenes and N-sulfinylanilines.
T2 - Angewandte Chemie - International Edition
AU - Jian, Tengyue
AU - He, Lin
AU - Tang, Cen
AU - Song Ye, Song
PY - 2011
DA - 2011/08/25
PB - Wiley
SP - 9104-9107
IS - 39
VL - 50
PMID - 21919141
SN - 1433-7851
SN - 1521-3773
ER -
Цитировать
BibTex (до 50 авторов)
Скопировать
@article{2011_Jian,
author = {Tengyue Jian and Lin He and Cen Tang and Song Song Ye},
title = {N-Heterocyclic carbene catalysis: enantioselective formal [2+2] cycloaddition of ketenes and N-sulfinylanilines.},
journal = {Angewandte Chemie - International Edition},
year = {2011},
volume = {50},
publisher = {Wiley},
month = {aug},
url = {https://doi.org/10.1002/anie.201102488},
number = {39},
pages = {9104--9107},
doi = {10.1002/anie.201102488}
}
Цитировать
MLA
Скопировать
Jian, Tengyue, et al. “N-Heterocyclic carbene catalysis: enantioselective formal [2+2] cycloaddition of ketenes and N-sulfinylanilines..” Angewandte Chemie - International Edition, vol. 50, no. 39, Aug. 2011, pp. 9104-9107. https://doi.org/10.1002/anie.201102488.
Ошибка в публикации?