Open Access
Open access
том 10 издание 45 страницы 10510-10515

Design, synthesis and application of a new type of bifunctional Le-Phos in highly enantioselective γ-addition reactions of N-centered nucleophiles to allenoates

Тип публикацииJournal Article
Дата публикации2019-09-03
SCImago Q1
Tоп 10% SCImago
WOS Q1
БС1
SJR2.011
CiteScore12
Impact factor8.1
ISSN20416520, 20416539
General Chemistry
Краткое описание
A novel class of cyclic phosphine derived bifunctional catalysts (Le-Phos) is reported, which can be readily prepared from inexpensive and commercially available starting materials and exhibit good performances in enantioselective γ-addition reactions of N-centered nucleophiles and allenoates under mild conditions. The salient features of this reaction include high product yields, good enantioselectivity, mild reaction conditions, and broad substrate scope and gram-scale scalability.
Для доступа к списку цитирований публикации необходимо авторизоваться.

Топ-30

Журналы

1
2
3
4
5
Organic Letters
5 публикаций, 20.83%
Chemical Communications
3 публикации, 12.5%
Science China Chemistry
2 публикации, 8.33%
Chemical Science
2 публикации, 8.33%
Russian Chemical Bulletin
2 публикации, 8.33%
Chinese Chemical Letters
1 публикация, 4.17%
ChemCatChem
1 публикация, 4.17%
ChemistrySelect
1 публикация, 4.17%
Chemistry - A European Journal
1 публикация, 4.17%
ACS Catalysis
1 публикация, 4.17%
ACS Central Science
1 публикация, 4.17%
ACS Sustainable Chemistry and Engineering
1 публикация, 4.17%
Organic Chemistry Frontiers
1 публикация, 4.17%
Asian Journal of Organic Chemistry
1 публикация, 4.17%
Chemical Reviews
1 публикация, 4.17%
1
2
3
4
5

Издатели

1
2
3
4
5
6
7
8
9
American Chemical Society (ACS)
9 публикаций, 37.5%
Royal Society of Chemistry (RSC)
6 публикаций, 25%
Springer Nature
4 публикации, 16.67%
Wiley
4 публикации, 16.67%
Elsevier
1 публикация, 4.17%
1
2
3
4
5
6
7
8
9
  • 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
24
Поделиться
Цитировать
ГОСТ |
Цитировать
Qiu H. et al. Design, synthesis and application of a new type of bifunctional Le-Phos in highly enantioselective γ-addition reactions of N-centered nucleophiles to allenoates // Chemical Science. 2019. Vol. 10. No. 45. pp. 10510-10515.
ГОСТ со всеми авторами (до 50) Скопировать
Qiu H., Chen X., Zhang J. Design, synthesis and application of a new type of bifunctional Le-Phos in highly enantioselective γ-addition reactions of N-centered nucleophiles to allenoates // Chemical Science. 2019. Vol. 10. No. 45. pp. 10510-10515.
RIS |
Цитировать
TY - JOUR
DO - 10.1039/c9sc04073k
UR - https://xlink.rsc.org/?DOI=C9SC04073K
TI - Design, synthesis and application of a new type of bifunctional Le-Phos in highly enantioselective γ-addition reactions of N-centered nucleophiles to allenoates
T2 - Chemical Science
AU - Qiu, Haile
AU - Chen, Xiaofeng
AU - Zhang, Junliang
PY - 2019
DA - 2019/09/03
PB - Royal Society of Chemistry (RSC)
SP - 10510-10515
IS - 45
VL - 10
PMID - 32055374
SN - 2041-6520
SN - 2041-6539
ER -
BibTex |
Цитировать
BibTex (до 50 авторов) Скопировать
@article{2019_Qiu,
author = {Haile Qiu and Xiaofeng Chen and Junliang Zhang},
title = {Design, synthesis and application of a new type of bifunctional Le-Phos in highly enantioselective γ-addition reactions of N-centered nucleophiles to allenoates},
journal = {Chemical Science},
year = {2019},
volume = {10},
publisher = {Royal Society of Chemistry (RSC)},
month = {sep},
url = {https://xlink.rsc.org/?DOI=C9SC04073K},
number = {45},
pages = {10510--10515},
doi = {10.1039/c9sc04073k}
}
MLA
Цитировать
Qiu, Haile, et al. “Design, synthesis and application of a new type of bifunctional Le-Phos in highly enantioselective γ-addition reactions of N-centered nucleophiles to allenoates.” Chemical Science, vol. 10, no. 45, Sep. 2019, pp. 10510-10515. https://xlink.rsc.org/?DOI=C9SC04073K.
Ошибка в публикации?