Exploiting Ancillary Ligation To Enable Nickel-Catalyzed C–O Cross-Couplings of Aryl Electrophiles with Aliphatic Alcohols
Publication type: Journal Article
Publication date: 2018-03-30
scimago Q1
wos Q1
SJR: 5.554
CiteScore: 22.5
Impact factor: 15.6
ISSN: 00027863, 15205126
PubMed ID:
29601188
General Chemistry
Catalysis
Biochemistry
Colloid and Surface Chemistry
Abstract
The use of (L)Ni( o-tolyl)Cl precatalysts (L = PAd-DalPhos or CyPAd-DalPhos) enables the C( sp2)-O cross-coupling of primary, secondary, or tertiary aliphatic alcohols with (hetero)aryl electrophiles, including unprecedented examples of such nickel-catalyzed transformations employing (hetero)aryl chlorides, sulfonates, and pivalates. In addition to offering a competitive alternative to palladium catalysis, this work establishes the feasibility of utilizing ancillary ligation as a complementary means of promoting challenging nickel-catalyzed C( sp2)-O cross-couplings, without recourse to precious-metal photoredox catalytic methods.
Found
Nothing found, try to update filter.
Found
Nothing found, try to update filter.
Top-30
Journals
|
2
4
6
8
10
12
14
|
|
|
ACS Catalysis
13 publications, 10.74%
|
|
|
Angewandte Chemie
12 publications, 9.92%
|
|
|
Angewandte Chemie - International Edition
12 publications, 9.92%
|
|
|
Organic Letters
10 publications, 8.26%
|
|
|
Journal of the American Chemical Society
7 publications, 5.79%
|
|
|
Chemistry - A European Journal
6 publications, 4.96%
|
|
|
Journal of Organic Chemistry
5 publications, 4.13%
|
|
|
Chemical Science
5 publications, 4.13%
|
|
|
Organometallics
4 publications, 3.31%
|
|
|
Chemical Communications
4 publications, 3.31%
|
|
|
Organic Chemistry Frontiers
4 publications, 3.31%
|
|
|
Advanced Synthesis and Catalysis
3 publications, 2.48%
|
|
|
Nature Communications
2 publications, 1.65%
|
|
|
ChemistrySelect
2 publications, 1.65%
|
|
|
Synlett
2 publications, 1.65%
|
|
|
European Journal of Organic Chemistry
2 publications, 1.65%
|
|
|
Organic Process Research and Development
2 publications, 1.65%
|
|
|
Journal of Chemical Research
1 publication, 0.83%
|
|
|
Catalysis Letters
1 publication, 0.83%
|
|
|
Chemical Record
1 publication, 0.83%
|
|
|
Journal of Organometallic Chemistry
1 publication, 0.83%
|
|
|
Materials Today: Proceedings
1 publication, 0.83%
|
|
|
Coordination Chemistry Reviews
1 publication, 0.83%
|
|
|
Nature Synthesis
1 publication, 0.83%
|
|
|
Journal of Porous Materials
1 publication, 0.83%
|
|
|
Inorganica Chimica Acta
1 publication, 0.83%
|
|
|
Chemistry - An Asian Journal
1 publication, 0.83%
|
|
|
European Journal of Inorganic Chemistry
1 publication, 0.83%
|
|
|
ChemCatChem
1 publication, 0.83%
|
|
|
Organic and Biomolecular Chemistry
1 publication, 0.83%
|
|
|
2
4
6
8
10
12
14
|
Publishers
|
5
10
15
20
25
30
35
40
45
|
|
|
American Chemical Society (ACS)
44 publications, 36.36%
|
|
|
Wiley
42 publications, 34.71%
|
|
|
Royal Society of Chemistry (RSC)
18 publications, 14.88%
|
|
|
Springer Nature
5 publications, 4.13%
|
|
|
Elsevier
4 publications, 3.31%
|
|
|
Georg Thieme Verlag KG
3 publications, 2.48%
|
|
|
SAGE
1 publication, 0.83%
|
|
|
MDPI
1 publication, 0.83%
|
|
|
OOO Zhurnal "Mendeleevskie Soobshcheniya"
1 publication, 0.83%
|
|
|
American Association for the Advancement of Science (AAAS)
1 publication, 0.83%
|
|
|
5
10
15
20
25
30
35
40
45
|
- 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
122
Total citations:
122
Citations from 2025:
17
(14.05%)
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Macqueen P. M. et al. Exploiting Ancillary Ligation To Enable Nickel-Catalyzed C–O Cross-Couplings of Aryl Electrophiles with Aliphatic Alcohols // Journal of the American Chemical Society. 2018. Vol. 140. No. 15. pp. 5023-5027.
GOST all authors (up to 50)
Copy
Macqueen P. M., Tassone J. P., Diaz C., Stradiotto M. Exploiting Ancillary Ligation To Enable Nickel-Catalyzed C–O Cross-Couplings of Aryl Electrophiles with Aliphatic Alcohols // Journal of the American Chemical Society. 2018. Vol. 140. No. 15. pp. 5023-5027.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1021/jacs.8b01800
UR - https://doi.org/10.1021/jacs.8b01800
TI - Exploiting Ancillary Ligation To Enable Nickel-Catalyzed C–O Cross-Couplings of Aryl Electrophiles with Aliphatic Alcohols
T2 - Journal of the American Chemical Society
AU - Macqueen, Preston M
AU - Tassone, Joseph P
AU - Diaz, Carlos
AU - Stradiotto, M.
PY - 2018
DA - 2018/03/30
PB - American Chemical Society (ACS)
SP - 5023-5027
IS - 15
VL - 140
PMID - 29601188
SN - 0002-7863
SN - 1520-5126
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2018_Macqueen,
author = {Preston M Macqueen and Joseph P Tassone and Carlos Diaz and M. Stradiotto},
title = {Exploiting Ancillary Ligation To Enable Nickel-Catalyzed C–O Cross-Couplings of Aryl Electrophiles with Aliphatic Alcohols},
journal = {Journal of the American Chemical Society},
year = {2018},
volume = {140},
publisher = {American Chemical Society (ACS)},
month = {mar},
url = {https://doi.org/10.1021/jacs.8b01800},
number = {15},
pages = {5023--5027},
doi = {10.1021/jacs.8b01800}
}
Cite this
MLA
Copy
Macqueen, Preston M., et al. “Exploiting Ancillary Ligation To Enable Nickel-Catalyzed C–O Cross-Couplings of Aryl Electrophiles with Aliphatic Alcohols.” Journal of the American Chemical Society, vol. 140, no. 15, Mar. 2018, pp. 5023-5027. https://doi.org/10.1021/jacs.8b01800.