,  том 50 ,  издание 18 ,  страницы 3421-3423

Stereocontrol in the intramolecular Diels-Alder reaction. 7. Use of the trimethylsilyl group as a removable stereocontrol element to provide greatly enhanced levels of diastereoselection

Тип публикации: Journal Article
Дата публикации: 1985-09-01
SCImago Q2
WOS Q1
БС1
SJR: 0.604
CiteScore: 5.8
Impact factor: 3.3
ISSN: 00223263, 15206904
Organic Chemistry
Краткое описание
L'introduction d'un groupe trimethylsilyl a des positions determinees dans des substrats trieniques subissant une cyclisation par cycloaddition Diels Alder intramoleculaire produisant des derives de l'indane ou de l'octahydronaphtalene conduit a une augmentation du niveau de diastereoselectivite
Для доступа к списку цитирований публикации необходимо авторизоваться.

Топ-30

Журналы

2
4
6
8
10
12
14
Tetrahedron Letters
13 публикаций, 16.67%
Tetrahedron
11 публикаций, 14.1%
Organic Letters
8 публикаций, 10.26%
Journal of the American Chemical Society
7 публикаций, 8.97%
Journal of Organic Chemistry
5 публикаций, 6.41%
Chemistry - A European Journal
3 публикации, 3.85%
Angewandte Chemie
3 публикации, 3.85%
Angewandte Chemie - International Edition
3 публикации, 3.85%
Chemical Communications
2 публикации, 2.56%
Organic and Biomolecular Chemistry
2 публикации, 2.56%
Palladium in Heterocyclic Chemistry - A Guide for the Synthetic Chemist
2 публикации, 2.56%
Proceedings of the National Academy of Sciences of the United States of America
2 публикации, 2.56%
Canadian Journal of Chemistry
1 публикация, 1.28%
Comptes Rendus de l Académie des Sciences - Series IIC - Chemistry
1 публикация, 1.28%
Russian Chemical Reviews
1 публикация, 1.28%
Journal of Organometallic Chemistry
1 публикация, 1.28%
Chemischer Informationsdienst
1 публикация, 1.28%
European Journal of Organic Chemistry
1 публикация, 1.28%
Chemical Reviews
1 публикация, 1.28%
Total Synthesis of Natural Products
1 публикация, 1.28%
Molecules
1 публикация, 1.28%
2
4
6
8
10
12
14

Издатели

5
10
15
20
25
30
35
Elsevier
31 публикация, 39.74%
American Chemical Society (ACS)
21 публикация, 26.92%
Wiley
12 публикаций, 15.38%
Royal Society of Chemistry (RSC)
4 публикации, 5.13%
Proceedings of the National Academy of Sciences (PNAS)
2 публикации, 2.56%
Canadian Science Publishing
1 публикация, 1.28%
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 публикация, 1.28%
MDPI
1 публикация, 1.28%
5
10
15
20
25
30
35
  • 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
78
Поделиться
Цитировать
ГОСТ |
Цитировать
Boeckman R. K., Barta T. E. Stereocontrol in the intramolecular Diels-Alder reaction. 7. Use of the trimethylsilyl group as a removable stereocontrol element to provide greatly enhanced levels of diastereoselection // Journal of Organic Chemistry. 1985. Vol. 50. No. 18. pp. 3421-3423.
ГОСТ со всеми авторами (до 50) Скопировать
Boeckman R. K., Barta T. E. Stereocontrol in the intramolecular Diels-Alder reaction. 7. Use of the trimethylsilyl group as a removable stereocontrol element to provide greatly enhanced levels of diastereoselection // Journal of Organic Chemistry. 1985. Vol. 50. No. 18. pp. 3421-3423.
RIS |
Цитировать
TY - JOUR
DO - 10.1021/jo00218a040
UR - https://doi.org/10.1021/jo00218a040
TI - Stereocontrol in the intramolecular Diels-Alder reaction. 7. Use of the trimethylsilyl group as a removable stereocontrol element to provide greatly enhanced levels of diastereoselection
T2 - Journal of Organic Chemistry
AU - Boeckman, Robert K.
AU - Barta, Thomas E
PY - 1985
DA - 1985/09/01
PB - American Chemical Society (ACS)
SP - 3421-3423
IS - 18
VL - 50
SN - 0022-3263
SN - 1520-6904
ER -
BibTex |
Цитировать
BibTex (до 50 авторов) Скопировать
@article{1985_Boeckman,
author = {Robert K. Boeckman and Thomas E Barta},
title = {Stereocontrol in the intramolecular Diels-Alder reaction. 7. Use of the trimethylsilyl group as a removable stereocontrol element to provide greatly enhanced levels of diastereoselection},
journal = {Journal of Organic Chemistry},
year = {1985},
volume = {50},
publisher = {American Chemical Society (ACS)},
month = {sep},
url = {https://doi.org/10.1021/jo00218a040},
number = {18},
pages = {3421--3423},
doi = {10.1021/jo00218a040}
}
MLA
Цитировать
Boeckman, Robert K., and Thomas E Barta. “Stereocontrol in the intramolecular Diels-Alder reaction. 7. Use of the trimethylsilyl group as a removable stereocontrol element to provide greatly enhanced levels of diastereoselection.” Journal of Organic Chemistry, vol. 50, no. 18, Sep. 1985, pp. 3421-3423. https://doi.org/10.1021/jo00218a040.
Ошибка в публикации?