volume 37 issue 8 pages 1423-1430

Cobalt-catalyzed redox-neutral synthesis of isoquinolines: C–H activation assisted by an oxidizing N–S bond

Publication typeJournal Article
Publication date2016-08-10
scimago Q1
wos Q1
SJR3.373
CiteScore24.8
Impact factor17.7
ISSN18722067, 02539837
Metals and Alloys
Mechanical Engineering
Mechanics of Materials
Abstract
A redox-neutral avenue to access isoquinolines has been realized by a Co(III)-catalyzed C–H activation process. Starting from readily available N -sulfinyl imine substrates and alkynes, the reaction occurred via N–S cleavage with broad substrate scope and functional group compatibility in the presence of cost-effective cobalt catalysts. A redox-neutral avenue to access isoquinolines has been realized by a Co(III)-catalyzed C–H activation process. Starting from readily available N-sulfinyl imine substrates and alkynes, the reaction occurred via N–S cleavage with broad substrate scope and functional group compatibility in the presence of a cost-effective cobalt catalyst.
Found 
Found 

Top-30

Journals

1
2
3
4
Tetrahedron
4 publications, 10.81%
Organic Letters
3 publications, 8.11%
Chemical Communications
3 publications, 8.11%
ACS Catalysis
2 publications, 5.41%
Chinese Journal of Catalysis
2 publications, 5.41%
Advanced Synthesis and Catalysis
2 publications, 5.41%
Journal of Organic Chemistry
2 publications, 5.41%
Mendeleev Communications
1 publication, 2.7%
ChemCatChem
1 publication, 2.7%
Asian Journal of Organic Chemistry
1 publication, 2.7%
Chemical Reviews
1 publication, 2.7%
ACS Omega
1 publication, 2.7%
Dalton Transactions
1 publication, 2.7%
Advances in Organometallic Chemistry
1 publication, 2.7%
Organic and Biomolecular Chemistry
1 publication, 2.7%
Synthetic Communications
1 publication, 2.7%
Synthesis
1 publication, 2.7%
Synlett
1 publication, 2.7%
ChemistrySelect
1 publication, 2.7%
1
2
3
4

Publishers

2
4
6
8
10
12
Wiley
11 publications, 29.73%
American Chemical Society (ACS)
9 publications, 24.32%
Elsevier
8 publications, 21.62%
Royal Society of Chemistry (RSC)
5 publications, 13.51%
Georg Thieme Verlag KG
2 publications, 5.41%
OOO Zhurnal "Mendeleevskie Soobshcheniya"
1 publication, 2.7%
Taylor & Francis
1 publication, 2.7%
2
4
6
8
10
12
  • We do not take into account publications without a DOI.
  • Statistics recalculated weekly.

Are you a researcher?

Create a profile to get free access to personal recommendations for colleagues and new articles.
Metrics
37
Share
Cite this
GOST |
Cite this
GOST Copy
Wang F. et al. Cobalt-catalyzed redox-neutral synthesis of isoquinolines: C–H activation assisted by an oxidizing N–S bond // Chinese Journal of Catalysis. 2016. Vol. 37. No. 8. pp. 1423-1430.
GOST all authors (up to 50) Copy
Wang F., Wang Q., Bao M., Li X. Cobalt-catalyzed redox-neutral synthesis of isoquinolines: C–H activation assisted by an oxidizing N–S bond // Chinese Journal of Catalysis. 2016. Vol. 37. No. 8. pp. 1423-1430.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/S1872-2067(16)62491-9
UR - https://linkinghub.elsevier.com/retrieve/pii/S1872206716624919
TI - Cobalt-catalyzed redox-neutral synthesis of isoquinolines: C–H activation assisted by an oxidizing N–S bond
T2 - Chinese Journal of Catalysis
AU - Wang, Fen
AU - Wang, Qiang
AU - Bao, Ming
AU - Li, Xingwei
PY - 2016
DA - 2016/08/10
PB - Elsevier
SP - 1423-1430
IS - 8
VL - 37
SN - 1872-2067
SN - 0253-9837
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2016_Wang,
author = {Fen Wang and Qiang Wang and Ming Bao and Xingwei Li},
title = {Cobalt-catalyzed redox-neutral synthesis of isoquinolines: C–H activation assisted by an oxidizing N–S bond},
journal = {Chinese Journal of Catalysis},
year = {2016},
volume = {37},
publisher = {Elsevier},
month = {aug},
url = {https://linkinghub.elsevier.com/retrieve/pii/S1872206716624919},
number = {8},
pages = {1423--1430},
doi = {10.1016/S1872-2067(16)62491-9}
}
MLA
Cite this
MLA Copy
Wang, Fen, et al. “Cobalt-catalyzed redox-neutral synthesis of isoquinolines: C–H activation assisted by an oxidizing N–S bond.” Chinese Journal of Catalysis, vol. 37, no. 8, Aug. 2016, pp. 1423-1430. https://linkinghub.elsevier.com/retrieve/pii/S1872206716624919.