Bifunctional Thiourea-Catalyzed Asymmetric Inverse-Electron-Demand Diels–Alder Reaction of Allyl Ketones and Vinyl 1,2-Diketones via Dienolate Intermediate
Тип публикации: Journal Article
Дата публикации: 2019-03-13
SCImago Q1
Tоп 10% SCImago
WOS Q1
БС1
SJR: 1.007
CiteScore: 7.7
Impact factor: 4.7
ISSN: 15237060, 15237052
PubMed ID:
30865466
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Краткое описание
Inverse-electron-demand Diels-Alder reactions have attracted intense research focus. However, enolate and enamine are the most employed intermediates to realize such transformation, and the use of dienolate intermediate remains elusive. Reported herein is the asymmetric inverse-electron-demand oxa-Diels-Alder reaction between allyl ketones and alkenyl 1,2-diketones using a bifunctional thiourea catalyst. The reaction afforded various highly functionalized dihydropyrans with good to excellent enantioselectivities under mild conditions, and further novel transformations on the products have also been realized.
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
|
1
2
3
4
5
6
7
8
9
|
|
|
Organic Letters
9 публикаций, 16.98%
|
|
|
Advanced Synthesis and Catalysis
6 публикаций, 11.32%
|
|
|
Asian Journal of Organic Chemistry
4 публикации, 7.55%
|
|
|
Chemistry - A European Journal
3 публикации, 5.66%
|
|
|
Journal of Organic Chemistry
3 публикации, 5.66%
|
|
|
Chemical Communications
3 публикации, 5.66%
|
|
|
Science China Chemistry
2 публикации, 3.77%
|
|
|
Angewandte Chemie
2 публикации, 3.77%
|
|
|
Angewandte Chemie - International Edition
2 публикации, 3.77%
|
|
|
Catalysts
1 публикация, 1.89%
|
|
|
Tetrahedron Letters
1 публикация, 1.89%
|
|
|
European Journal of Organic Chemistry
1 публикация, 1.89%
|
|
|
ChemSusChem
1 публикация, 1.89%
|
|
|
ACS Catalysis
1 публикация, 1.89%
|
|
|
Chemical Society Reviews
1 публикация, 1.89%
|
|
|
Green Chemistry
1 публикация, 1.89%
|
|
|
Progress in Heterocyclic Chemistry
1 публикация, 1.89%
|
|
|
Heterocycles
1 публикация, 1.89%
|
|
|
Organic and Biomolecular Chemistry
1 публикация, 1.89%
|
|
|
New Journal of Chemistry
1 публикация, 1.89%
|
|
|
Green Synthesis and Catalysis
1 публикация, 1.89%
|
|
|
Journal of the American Chemical Society
1 публикация, 1.89%
|
|
|
Current Organic Synthesis
1 публикация, 1.89%
|
|
|
Russian Journal of Organic Chemistry
1 публикация, 1.89%
|
|
|
ChemCatChem
1 публикация, 1.89%
|
|
|
Synthesis
1 публикация, 1.89%
|
|
|
Canadian Journal of Chemistry
1 публикация, 1.89%
|
|
|
Russian Chemical Reviews
1 публикация, 1.89%
|
|
|
1
2
3
4
5
6
7
8
9
|
Издатели
|
5
10
15
20
|
|
|
Wiley
20 публикаций, 37.74%
|
|
|
American Chemical Society (ACS)
14 публикаций, 26.42%
|
|
|
Royal Society of Chemistry (RSC)
7 публикаций, 13.21%
|
|
|
Elsevier
3 публикации, 5.66%
|
|
|
Springer Nature
2 публикации, 3.77%
|
|
|
MDPI
1 публикация, 1.89%
|
|
|
The Japan Institute of Heterocyclic Chemistry
1 публикация, 1.89%
|
|
|
Bentham Science Publishers Ltd.
1 публикация, 1.89%
|
|
|
Pleiades Publishing
1 публикация, 1.89%
|
|
|
Georg Thieme Verlag KG
1 публикация, 1.89%
|
|
|
Canadian Science Publishing
1 публикация, 1.89%
|
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 публикация, 1.89%
|
|
|
5
10
15
20
|
- 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
53
Всего цитирований:
53
Цитирований c 2025:
8
(15.09%)
Цитировать
ГОСТ |
RIS |
BibTex |
MLA
Цитировать
ГОСТ
Скопировать
Li Xinglong X. et al. Bifunctional Thiourea-Catalyzed Asymmetric Inverse-Electron-Demand Diels–Alder Reaction of Allyl Ketones and Vinyl 1,2-Diketones via Dienolate Intermediate // Organic Letters. 2019. Vol. 21. No. 7. pp. 1979-1983.
ГОСТ со всеми авторами (до 50)
Скопировать
Li Xinglong X., Kong X., Yang S., Meng M., Zhan X., Zeng M., Fang X. Bifunctional Thiourea-Catalyzed Asymmetric Inverse-Electron-Demand Diels–Alder Reaction of Allyl Ketones and Vinyl 1,2-Diketones via Dienolate Intermediate // Organic Letters. 2019. Vol. 21. No. 7. pp. 1979-1983.
Цитировать
RIS
Скопировать
TY - JOUR
DO - 10.1021/acs.orglett.9b00035
UR - https://doi.org/10.1021/acs.orglett.9b00035
TI - Bifunctional Thiourea-Catalyzed Asymmetric Inverse-Electron-Demand Diels–Alder Reaction of Allyl Ketones and Vinyl 1,2-Diketones via Dienolate Intermediate
T2 - Organic Letters
AU - Li Xinglong, Xinglong
AU - Kong, Xiangwen
AU - Yang, Shuang
AU - Meng, Miao
AU - Zhan, Xinyue
AU - Zeng, Min
AU - Fang, Xinqiang
PY - 2019
DA - 2019/03/13
PB - American Chemical Society (ACS)
SP - 1979-1983
IS - 7
VL - 21
PMID - 30865466
SN - 1523-7060
SN - 1523-7052
ER -
Цитировать
BibTex (до 50 авторов)
Скопировать
@article{2019_Li Xinglong,
author = {Xinglong Li Xinglong and Xiangwen Kong and Shuang Yang and Miao Meng and Xinyue Zhan and Min Zeng and Xinqiang Fang},
title = {Bifunctional Thiourea-Catalyzed Asymmetric Inverse-Electron-Demand Diels–Alder Reaction of Allyl Ketones and Vinyl 1,2-Diketones via Dienolate Intermediate},
journal = {Organic Letters},
year = {2019},
volume = {21},
publisher = {American Chemical Society (ACS)},
month = {mar},
url = {https://doi.org/10.1021/acs.orglett.9b00035},
number = {7},
pages = {1979--1983},
doi = {10.1021/acs.orglett.9b00035}
}
Цитировать
MLA
Скопировать
Li Xinglong, Xinglong, et al. “Bifunctional Thiourea-Catalyzed Asymmetric Inverse-Electron-Demand Diels–Alder Reaction of Allyl Ketones and Vinyl 1,2-Diketones via Dienolate Intermediate.” Organic Letters, vol. 21, no. 7, Mar. 2019, pp. 1979-1983. https://doi.org/10.1021/acs.orglett.9b00035.
Ошибка в публикации?