том 72 издание 27-28 страницы 4123-4131

One-pot synthesis of polyhydropyrido[1,2- a ]indoles and tetracyclic quinazolinones from 2-arylindoles using copper-mediated oxidative tandem reactions

Тип публикацииJournal Article
Дата публикации2016-07-01
scimago Q3
wos Q2
БС2
SJR0.426
CiteScore4.1
Impact factor2.2
ISSN00404020, 14645416
Organic Chemistry
Drug Discovery
Biochemistry
Краткое описание
We developed facile one-pot methods for the transformation of 2-arylindoles to polyhydropyrido[1,2-a]indoles and tetracyclic quinazolinones. The copper-catalyzed oxidation of 2-arylindoles to C-acylimines followed by aza-Diels–Alder reactions or oxidative ring-expansion reactions afforded significant polycyclic heterocycles.
Найдено 
Для доступа к списку цитирований публикации необходимо авторизоваться.

Топ-30

Журналы

1
2
3
4
Chemical Communications
4 публикации, 13.33%
Journal of Organic Chemistry
3 публикации, 10%
Organic Letters
3 публикации, 10%
Organic Chemistry Frontiers
3 публикации, 10%
Molecules
2 публикации, 6.67%
Advanced Synthesis and Catalysis
2 публикации, 6.67%
Organic and Biomolecular Chemistry
2 публикации, 6.67%
Chinese Journal of Organic Chemistry
1 публикация, 3.33%
Monatshefte fur Chemie
1 публикация, 3.33%
Mendeleev Communications
1 публикация, 3.33%
ChemInform
1 публикация, 3.33%
ChemistrySelect
1 публикация, 3.33%
Asian Journal of Organic Chemistry
1 публикация, 3.33%
ACS Catalysis
1 публикация, 3.33%
RSC Advances
1 публикация, 3.33%
Synthesis
1 публикация, 3.33%
SynOpen
1 публикация, 3.33%
Chinese Chemical Letters
1 публикация, 3.33%
1
2
3
4

Издатели

2
4
6
8
10
Royal Society of Chemistry (RSC)
10 публикаций, 33.33%
American Chemical Society (ACS)
7 публикаций, 23.33%
Wiley
5 публикаций, 16.67%
MDPI
2 публикации, 6.67%
Georg Thieme Verlag KG
2 публикации, 6.67%
Shanghai Institute of Organic Chemistry
1 публикация, 3.33%
Springer Nature
1 публикация, 3.33%
OOO Zhurnal "Mendeleevskie Soobshcheniya"
1 публикация, 3.33%
Elsevier
1 публикация, 3.33%
2
4
6
8
10
  • 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
30
Поделиться
Цитировать
ГОСТ |
Цитировать
Yamashita M. et al. One-pot synthesis of polyhydropyrido[1,2- a ]indoles and tetracyclic quinazolinones from 2-arylindoles using copper-mediated oxidative tandem reactions // Tetrahedron. 2016. Vol. 72. No. 27-28. pp. 4123-4131.
ГОСТ со всеми авторами (до 50) Скопировать
Yamashita M., Nishizono Y., Himekawa S., Iida A. One-pot synthesis of polyhydropyrido[1,2- a ]indoles and tetracyclic quinazolinones from 2-arylindoles using copper-mediated oxidative tandem reactions // Tetrahedron. 2016. Vol. 72. No. 27-28. pp. 4123-4131.
RIS |
Цитировать
TY - JOUR
DO - 10.1016/j.tet.2016.05.054
UR - https://doi.org/10.1016/j.tet.2016.05.054
TI - One-pot synthesis of polyhydropyrido[1,2- a ]indoles and tetracyclic quinazolinones from 2-arylindoles using copper-mediated oxidative tandem reactions
T2 - Tetrahedron
AU - Yamashita, Mitsuaki
AU - Nishizono, Yukari
AU - Himekawa, Seiya
AU - Iida, Akira
PY - 2016
DA - 2016/07/01
PB - Elsevier
SP - 4123-4131
IS - 27-28
VL - 72
SN - 0040-4020
SN - 1464-5416
ER -
BibTex |
Цитировать
BibTex (до 50 авторов) Скопировать
@article{2016_Yamashita,
author = {Mitsuaki Yamashita and Yukari Nishizono and Seiya Himekawa and Akira Iida},
title = {One-pot synthesis of polyhydropyrido[1,2- a ]indoles and tetracyclic quinazolinones from 2-arylindoles using copper-mediated oxidative tandem reactions},
journal = {Tetrahedron},
year = {2016},
volume = {72},
publisher = {Elsevier},
month = {jul},
url = {https://doi.org/10.1016/j.tet.2016.05.054},
number = {27-28},
pages = {4123--4131},
doi = {10.1016/j.tet.2016.05.054}
}
MLA
Цитировать
Yamashita, Mitsuaki, et al. “One-pot synthesis of polyhydropyrido[1,2- a ]indoles and tetracyclic quinazolinones from 2-arylindoles using copper-mediated oxidative tandem reactions.” Tetrahedron, vol. 72, no. 27-28, Jul. 2016, pp. 4123-4131. https://doi.org/10.1016/j.tet.2016.05.054.