Ugi Reactions with Ammonia Offer Rapid Access to a Wide Range of 5-Aminothiazole and Oxazole Derivatives
Тип публикации: Journal Article
Дата публикации: 2009-08-25
scimago Q2
wos Q1
БС1
SJR: 0.737
CiteScore: 6.1
Impact factor: 3.6
ISSN: 00223263, 15206904
PubMed ID:
19705810
Organic Chemistry
Краткое описание
A series of Ugi reactions has been successfully performed using ammonia as the amine component, employing 2,2,2-trifluoroethanol as a non-nucleophilic solvent in order to suppress known side reactions. Utilizing concentrated aqueous ammonia as a convenient source, this approach offered a simple, one-step assembly of Ugi adducts suitable for elaboration into a variety of 5-aminoazole compounds through postcondensation modifications. Free or N-substituted 5-aminothiazoles and 5-(trifluoroacetamido)oxazoles were all prepared by this improved methodology. The scope of the synthetic route developed and application of the different products are discussed.
Найдено
Ничего не найдено, попробуйте изменить настройки фильтра.
Для доступа к списку цитирований публикации необходимо авторизоваться.
Топ-30
Журналы
|
1
2
3
4
5
6
|
|
|
Journal of Organic Chemistry
6 публикаций, 9.52%
|
|
|
Organic Letters
5 публикаций, 7.94%
|
|
|
Organic and Biomolecular Chemistry
4 публикации, 6.35%
|
|
|
Tetrahedron Letters
3 публикации, 4.76%
|
|
|
European Journal of Medicinal Chemistry
3 публикации, 4.76%
|
|
|
Tetrahedron
2 публикации, 3.17%
|
|
|
Advanced Synthesis and Catalysis
2 публикации, 3.17%
|
|
|
Chemistry - A European Journal
2 публикации, 3.17%
|
|
|
Chemical Reviews
2 публикации, 3.17%
|
|
|
ACS Combinatorial Science
2 публикации, 3.17%
|
|
|
Progress in Heterocyclic Chemistry
2 публикации, 3.17%
|
|
|
Synthesis
2 публикации, 3.17%
|
|
|
Beilstein Journal of Organic Chemistry
1 публикация, 1.59%
|
|
|
Molecules
1 публикация, 1.59%
|
|
|
EJNMMI Radiopharmacy and Chemistry
1 публикация, 1.59%
|
|
|
Journal of the Iranian Chemical Society
1 публикация, 1.59%
|
|
|
Bioorganic and Medicinal Chemistry
1 публикация, 1.59%
|
|
|
Bioorganic and Medicinal Chemistry Letters
1 публикация, 1.59%
|
|
|
Chinese Chemical Letters
1 публикация, 1.59%
|
|
|
Mendeleev Communications
1 публикация, 1.59%
|
|
|
ChemCatChem
1 публикация, 1.59%
|
|
|
Angewandte Chemie - International Edition
1 публикация, 1.59%
|
|
|
Angewandte Chemie
1 публикация, 1.59%
|
|
|
ChemInform
1 публикация, 1.59%
|
|
|
Journal of the American Chemical Society
1 публикация, 1.59%
|
|
|
Journal of Medicinal Chemistry
1 публикация, 1.59%
|
|
|
ACS Omega
1 публикация, 1.59%
|
|
|
MedChemComm
1 публикация, 1.59%
|
|
|
Chemical Society Reviews
1 публикация, 1.59%
|
|
|
1
2
3
4
5
6
|
Издатели
|
2
4
6
8
10
12
14
16
18
|
|
|
American Chemical Society (ACS)
18 публикаций, 28.57%
|
|
|
Elsevier
13 публикаций, 20.63%
|
|
|
Wiley
12 публикаций, 19.05%
|
|
|
Royal Society of Chemistry (RSC)
6 публикаций, 9.52%
|
|
|
Springer Nature
5 публикаций, 7.94%
|
|
|
Taylor & Francis
2 публикации, 3.17%
|
|
|
Georg Thieme Verlag KG
2 публикации, 3.17%
|
|
|
Beilstein-Institut
1 публикация, 1.59%
|
|
|
MDPI
1 публикация, 1.59%
|
|
|
OOO Zhurnal "Mendeleevskie Soobshcheniya"
1 публикация, 1.59%
|
|
|
Proceedings of the National Academy of Sciences (PNAS)
1 публикация, 1.59%
|
|
|
2
4
6
8
10
12
14
16
18
|
- 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
63
Всего цитирований:
63
Цитирований c 2025:
1
(1.59%)
Цитировать
ГОСТ |
RIS |
BibTex |
MLA
Цитировать
ГОСТ
Скопировать
Thompson M. J., Chen B. Ugi Reactions with Ammonia Offer Rapid Access to a Wide Range of 5-Aminothiazole and Oxazole Derivatives // Journal of Organic Chemistry. 2009. Vol. 74. No. 18. pp. 7084-7093.
ГОСТ со всеми авторами (до 50)
Скопировать
Thompson M. J., Chen B. Ugi Reactions with Ammonia Offer Rapid Access to a Wide Range of 5-Aminothiazole and Oxazole Derivatives // Journal of Organic Chemistry. 2009. Vol. 74. No. 18. pp. 7084-7093.
Цитировать
RIS
Скопировать
TY - JOUR
DO - 10.1021/jo9014529
UR - https://doi.org/10.1021/jo9014529
TI - Ugi Reactions with Ammonia Offer Rapid Access to a Wide Range of 5-Aminothiazole and Oxazole Derivatives
T2 - Journal of Organic Chemistry
AU - Thompson, Mark J.
AU - Chen, B.
PY - 2009
DA - 2009/08/25
PB - American Chemical Society (ACS)
SP - 7084-7093
IS - 18
VL - 74
PMID - 19705810
SN - 0022-3263
SN - 1520-6904
ER -
Цитировать
BibTex (до 50 авторов)
Скопировать
@article{2009_Thompson,
author = {Mark J. Thompson and B. Chen},
title = {Ugi Reactions with Ammonia Offer Rapid Access to a Wide Range of 5-Aminothiazole and Oxazole Derivatives},
journal = {Journal of Organic Chemistry},
year = {2009},
volume = {74},
publisher = {American Chemical Society (ACS)},
month = {aug},
url = {https://doi.org/10.1021/jo9014529},
number = {18},
pages = {7084--7093},
doi = {10.1021/jo9014529}
}
Цитировать
MLA
Скопировать
Thompson, Mark J., and B. Chen. “Ugi Reactions with Ammonia Offer Rapid Access to a Wide Range of 5-Aminothiazole and Oxazole Derivatives.” Journal of Organic Chemistry, vol. 74, no. 18, Aug. 2009, pp. 7084-7093. https://doi.org/10.1021/jo9014529.