Enantioselective direct aldol reaction of α-keto esters catalyzed by (Sa)-binam-d-prolinamide under quasi solvent-free conditions
Тип публикации: Journal Article
Дата публикации: 2012-03-23
scimago Q2
wos Q2
БС1
SJR: 0.6
CiteScore: 5.2
Impact factor: 2.7
ISSN: 14770520, 14770539
PubMed ID:
22514086
Organic Chemistry
Biochemistry
Physical and Theoretical Chemistry
Краткое описание
(S(a))-Binam-D-prolinamide (20 mol%), instead of (S(a))-binam-L-prolinamide, in combination with chloroacetic acid (100 mol%) is an efficient organocatalyst for the direct aldol reaction between α-keto esters as electrophiles and alkyl and α-functionalised ketones, under quasi solvent-free conditions, providing access to highly functionalised chiral quaternary γ-keto α-hydroxyesters with up to 92% ee.
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
|
|
|
Tetrahedron Asymmetry
4 публикации, 13.79%
|
|
|
Chemistry - A European Journal
4 публикации, 13.79%
|
|
|
RSC Advances
3 публикации, 10.34%
|
|
|
Synlett
2 публикации, 6.9%
|
|
|
Molecules
1 публикация, 3.45%
|
|
|
Catalysts
1 публикация, 3.45%
|
|
|
Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry
1 публикация, 3.45%
|
|
|
Mendeleev Communications
1 публикация, 3.45%
|
|
|
ChemistrySelect
1 публикация, 3.45%
|
|
|
ChemInform
1 публикация, 3.45%
|
|
|
Angewandte Chemie
1 публикация, 3.45%
|
|
|
Angewandte Chemie - International Edition
1 публикация, 3.45%
|
|
|
Chirality
1 публикация, 3.45%
|
|
|
Organic Letters
1 публикация, 3.45%
|
|
|
Journal of Organic Chemistry
1 публикация, 3.45%
|
|
|
Organic and Biomolecular Chemistry
1 публикация, 3.45%
|
|
|
Chemical Communications
1 публикация, 3.45%
|
|
|
Synthesis
1 публикация, 3.45%
|
|
|
Asian Journal of Organic Chemistry
1 публикация, 3.45%
|
|
|
1
2
3
4
|
Издатели
|
2
4
6
8
10
12
|
|
|
Wiley
11 публикаций, 37.93%
|
|
|
Royal Society of Chemistry (RSC)
5 публикаций, 17.24%
|
|
|
Elsevier
4 публикации, 13.79%
|
|
|
Georg Thieme Verlag KG
3 публикации, 10.34%
|
|
|
MDPI
2 публикации, 6.9%
|
|
|
American Chemical Society (ACS)
2 публикации, 6.9%
|
|
|
The Society of Synthetic Organic Chemistry, Japan
1 публикация, 3.45%
|
|
|
OOO Zhurnal "Mendeleevskie Soobshcheniya"
1 публикация, 3.45%
|
|
|
2
4
6
8
10
12
|
- 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
29
Всего цитирований:
29
Цитирований c 2025:
1
(3.45%)
Цитировать
ГОСТ |
RIS |
BibTex |
MLA
Цитировать
ГОСТ
Скопировать
Viózquez S. F. et al. Enantioselective direct aldol reaction of α-keto esters catalyzed by (Sa)-binam-d-prolinamide under quasi solvent-free conditions // Organic and Biomolecular Chemistry. 2012. Vol. 10. No. 20. p. 4029.
ГОСТ со всеми авторами (до 50)
Скопировать
Viózquez S. F., Bañón Caballero A., Bañón-Caballero A., Guillena G., Nájera C., Gómez-Bengoa E. Enantioselective direct aldol reaction of α-keto esters catalyzed by (Sa)-binam-d-prolinamide under quasi solvent-free conditions // Organic and Biomolecular Chemistry. 2012. Vol. 10. No. 20. p. 4029.
Цитировать
RIS
Скопировать
TY - JOUR
DO - 10.1039/c2ob25224d
UR - https://doi.org/10.1039/c2ob25224d
TI - Enantioselective direct aldol reaction of α-keto esters catalyzed by (Sa)-binam-d-prolinamide under quasi solvent-free conditions
T2 - Organic and Biomolecular Chemistry
AU - Viózquez, Santiago F
AU - Bañón Caballero, Abraham
AU - Bañón-Caballero, Abraham
AU - Guillena, Gabriela
AU - Nájera, Carmen
AU - Gómez-Bengoa, Enrique
PY - 2012
DA - 2012/03/23
PB - Royal Society of Chemistry (RSC)
SP - 4029
IS - 20
VL - 10
PMID - 22514086
SN - 1477-0520
SN - 1477-0539
ER -
Цитировать
BibTex (до 50 авторов)
Скопировать
@article{2012_Viózquez,
author = {Santiago F Viózquez and Abraham Bañón Caballero and Abraham Bañón-Caballero and Gabriela Guillena and Carmen Nájera and Enrique Gómez-Bengoa},
title = {Enantioselective direct aldol reaction of α-keto esters catalyzed by (Sa)-binam-d-prolinamide under quasi solvent-free conditions},
journal = {Organic and Biomolecular Chemistry},
year = {2012},
volume = {10},
publisher = {Royal Society of Chemistry (RSC)},
month = {mar},
url = {https://doi.org/10.1039/c2ob25224d},
number = {20},
pages = {4029},
doi = {10.1039/c2ob25224d}
}
Цитировать
MLA
Скопировать
Viózquez, Santiago F., et al. “Enantioselective direct aldol reaction of α-keto esters catalyzed by (Sa)-binam-d-prolinamide under quasi solvent-free conditions.” Organic and Biomolecular Chemistry, vol. 10, no. 20, Mar. 2012, p. 4029. https://doi.org/10.1039/c2ob25224d.