том 48 издание 8 страницы 2354-2365

Advances in Nickel-Catalyzed Cycloaddition Reactions To Construct Carbocycles and Heterocycles

Тип публикацииJournal Article
Дата публикации2015-07-22
scimago Q1
wos Q1
БС1
SJR5.433
CiteScore30.7
Impact factor17.7
ISSN00014842, 15204898
General Chemistry
General Medicine
Краткое описание
Transition-metal catalysis has revolutionized the field of organic synthesis by facilitating the construction of complex organic molecules in a highly efficient manner. Although these catalysts are typically based on precious metals, researchers have made great strides in discovering new base metal catalysts over the past decade. This Account describes our efforts in this area and details the development of versatile Ni complexes that catalyze a variety of cycloaddition reactions to afford interesting carbocycles and heterocycles. First, we describe our early work in investigating the efficacy of N-heterocyclic carbene (NHC) ligands in Ni-catalyzed cycloaddition reactions with carbon dioxide and isocyanate. The use of sterically hindered, electron donating NHC ligands in these reactions significantly improved the substrate scope as well as reaction conditions in the syntheses of a variety of pyrones and pyridones. The high reactivity and versatility of these unique Ni(NHC) catalytic systems allowed us to develop unprecedented Ni-catalyzed cycloadditions that were unexplored due to the inefficacy of early Ni catalysts to promote hetero-oxidative coupling steps. We describe the development and mechanistic analysis of Ni/NHC catalysts that couple diynes and nitriles to form pyridines. Kinetic studies and stoichiometric reactions confirmed a hetero-oxidative coupling pathway associated with this Ni-catalyzed cycloaddition. We then describe a series of new substrates for Ni-catalyzed cycloaddition reactions such as vinylcyclopropanes, aldehydes, ketones, tropones, 3-azetidinones, and 3-oxetanones. In reactions with vinycyclopropanes and tropones, DFT calculations reveal noteworthy mechanistic steps such as a C-C σ-bond activation and an 8π-insertion of vinylcyclopropane and tropone, respectively. Similarly, the cycloaddition of 3-azetidinones and 3-oxetanones also requires Ni-catalyzed C-C σ-bond activation to form N- and O-containing heterocycles.
Найдено 
Для доступа к списку цитирований публикации необходимо авторизоваться.

Топ-30

Журналы

2
4
6
8
10
ACS Catalysis
10 публикаций, 7.52%
Advanced Synthesis and Catalysis
10 публикаций, 7.52%
Organic Letters
9 публикаций, 6.77%
Chemistry - A European Journal
6 публикаций, 4.51%
Journal of Organic Chemistry
6 публикаций, 4.51%
Organometallics
6 публикаций, 4.51%
Journal of the American Chemical Society
5 публикаций, 3.76%
Chemical Reviews
5 публикаций, 3.76%
Organic and Biomolecular Chemistry
5 публикаций, 3.76%
RSC Advances
5 публикаций, 3.76%
Angewandte Chemie
4 публикации, 3.01%
Angewandte Chemie - International Edition
4 публикации, 3.01%
European Journal of Organic Chemistry
4 публикации, 3.01%
Dalton Transactions
4 публикации, 3.01%
Organic Chemistry Frontiers
4 публикации, 3.01%
Synthesis
4 публикации, 3.01%
Chemical Communications
3 публикации, 2.26%
Chem
2 публикации, 1.5%
Asian Journal of Organic Chemistry
2 публикации, 1.5%
Catalysis Science and Technology
2 публикации, 1.5%
Chinese Journal of Chemistry
2 публикации, 1.5%
ChemistrySelect
2 публикации, 1.5%
Molecules
1 публикация, 0.75%
Catalysts
1 публикация, 0.75%
Communications Chemistry
1 публикация, 0.75%
Tetrahedron Letters
1 публикация, 0.75%
Chem Catalysis
1 публикация, 0.75%
Journal of Fluorine Chemistry
1 публикация, 0.75%
Applied Catalysis A: General
1 публикация, 0.75%
2
4
6
8
10

Издатели

5
10
15
20
25
30
35
40
45
American Chemical Society (ACS)
44 публикации, 33.08%
Wiley
44 публикации, 33.08%
Royal Society of Chemistry (RSC)
23 публикации, 17.29%
Elsevier
12 публикаций, 9.02%
Georg Thieme Verlag KG
4 публикации, 3.01%
MDPI
2 публикации, 1.5%
Springer Nature
2 публикации, 1.5%
OOO Zhurnal "Mendeleevskie Soobshcheniya"
1 публикация, 0.75%
De Gruyter Brill
1 публикация, 0.75%
5
10
15
20
25
30
35
40
45
  • 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
133
Поделиться
Цитировать
ГОСТ |
Цитировать
Thakur A., Louie J. Advances in Nickel-Catalyzed Cycloaddition Reactions To Construct Carbocycles and Heterocycles // Accounts of Chemical Research. 2015. Vol. 48. No. 8. pp. 2354-2365.
ГОСТ со всеми авторами (до 50) Скопировать
Thakur A., Louie J. Advances in Nickel-Catalyzed Cycloaddition Reactions To Construct Carbocycles and Heterocycles // Accounts of Chemical Research. 2015. Vol. 48. No. 8. pp. 2354-2365.
RIS |
Цитировать
TY - JOUR
DO - 10.1021/acs.accounts.5b00054
UR - https://doi.org/10.1021/acs.accounts.5b00054
TI - Advances in Nickel-Catalyzed Cycloaddition Reactions To Construct Carbocycles and Heterocycles
T2 - Accounts of Chemical Research
AU - Thakur, Ashish
AU - Louie, Janis
PY - 2015
DA - 2015/07/22
PB - American Chemical Society (ACS)
SP - 2354-2365
IS - 8
VL - 48
PMID - 26200651
SN - 0001-4842
SN - 1520-4898
ER -
BibTex |
Цитировать
BibTex (до 50 авторов) Скопировать
@article{2015_Thakur,
author = {Ashish Thakur and Janis Louie},
title = {Advances in Nickel-Catalyzed Cycloaddition Reactions To Construct Carbocycles and Heterocycles},
journal = {Accounts of Chemical Research},
year = {2015},
volume = {48},
publisher = {American Chemical Society (ACS)},
month = {jul},
url = {https://doi.org/10.1021/acs.accounts.5b00054},
number = {8},
pages = {2354--2365},
doi = {10.1021/acs.accounts.5b00054}
}
MLA
Цитировать
Thakur, Ashish, and Janis Louie. “Advances in Nickel-Catalyzed Cycloaddition Reactions To Construct Carbocycles and Heterocycles.” Accounts of Chemical Research, vol. 48, no. 8, Jul. 2015, pp. 2354-2365. https://doi.org/10.1021/acs.accounts.5b00054.