Angewandte Chemie - International Edition, volume 53, issue 35, pages 9142-9150
Catalytic Enantioselective CH Functionalization of Alcohols by Redox-Triggered Carbonyl Addition: Borrowing Hydrogen, Returning Carbon
Publication type: Journal Article
Publication date: 2014-07-23
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor: 16.6
ISSN: 14337851, 15213773
General Chemistry
Catalysis
Abstract
The use of alcohols and unsaturated reactants for the redox-triggered generation of nucleophile-electrophile pairs represents a broad, new approach to carbonyl addition chemistry. Discrete redox manipulations that are often required for the generation of carbonyl electrophiles and premetalated carbon-centered nucleophiles are thus avoided. Based on this concept, a broad, new family of enantioselective C-C coupling reactions that are catalyzed by iridium or ruthenium complexes have been developed, which are summarized in this Minireview.
Top-30
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1 publication, 0.32%
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Citations by publishers
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Wiley
134 publications, 43.37%
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American Chemical Society (ACS)
116 publications, 37.54%
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31 publications, 10.03%
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Elsevier
10 publications, 3.24%
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7 publications, 2.27%
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Springer Nature
4 publications, 1.29%
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American Association for the Advancement of Science (AAAS)
2 publications, 0.65%
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Beilstein-Institut
1 publication, 0.32%
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The Chemical Society of Japan
1 publication, 0.32%
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King Saud University
1 publication, 0.32%
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Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 0.32%
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- We do not take into account publications without a DOI.
- Statistics recalculated only for publications connected to researchers, organizations and labs registered on the platform.
- Statistics recalculated weekly.
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Ketcham J. M. et al. Catalytic Enantioselective CH Functionalization of Alcohols by Redox-Triggered Carbonyl Addition: Borrowing Hydrogen, Returning Carbon // Angewandte Chemie - International Edition. 2014. Vol. 53. No. 35. pp. 9142-9150.
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Ketcham J. M., Shin I., Montgomery T. P., Krische M. J. Catalytic Enantioselective CH Functionalization of Alcohols by Redox-Triggered Carbonyl Addition: Borrowing Hydrogen, Returning Carbon // Angewandte Chemie - International Edition. 2014. Vol. 53. No. 35. pp. 9142-9150.
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TY - JOUR
DO - 10.1002/anie.201403873
UR - https://doi.org/10.1002/anie.201403873
TI - Catalytic Enantioselective CH Functionalization of Alcohols by Redox-Triggered Carbonyl Addition: Borrowing Hydrogen, Returning Carbon
T2 - Angewandte Chemie - International Edition
AU - Ketcham, John M
AU - Shin, Inji
AU - Montgomery, T Patrick
AU - Krische, Michael J
PY - 2014
DA - 2014/07/23 00:00:00
PB - Wiley
SP - 9142-9150
IS - 35
VL - 53
SN - 1433-7851
SN - 1521-3773
ER -
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@article{2014_Ketcham,
author = {John M Ketcham and Inji Shin and T Patrick Montgomery and Michael J Krische},
title = {Catalytic Enantioselective CH Functionalization of Alcohols by Redox-Triggered Carbonyl Addition: Borrowing Hydrogen, Returning Carbon},
journal = {Angewandte Chemie - International Edition},
year = {2014},
volume = {53},
publisher = {Wiley},
month = {jul},
url = {https://doi.org/10.1002/anie.201403873},
number = {35},
pages = {9142--9150},
doi = {10.1002/anie.201403873}
}
Cite this
MLA
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Ketcham, John M., et al. “Catalytic Enantioselective CH Functionalization of Alcohols by Redox-Triggered Carbonyl Addition: Borrowing Hydrogen, Returning Carbon.” Angewandte Chemie - International Edition, vol. 53, no. 35, Jul. 2014, pp. 9142-9150. https://doi.org/10.1002/anie.201403873.