A Fluorinated Ligand Enables Room-Temperature and Regioselective Pd-Catalyzed Fluorination of Aryl Triflates and Bromides
Тип публикации: Journal Article
Дата публикации: 2015-10-06
scimago Q1
wos Q1
БС1
SJR: 5.554
CiteScore: 22.5
Impact factor: 15.6
ISSN: 00027863, 15205126
PubMed ID:
26413908
General Chemistry
Catalysis
Biochemistry
Colloid and Surface Chemistry
Краткое описание
A new biaryl monophosphine ligand (AlPhos, L1) allows for the room-temperature Pd-catalyzed fluorination of a variety of activated (hetero)aryl triflates. Furthermore, aryl triflates and bromides that are prone to give mixtures of regioisomeric aryl fluorides with Pd-catalysis can now be converted to the desired aryl fluorides with high regioselectivity. Analysis of the solid-state structures of several Pd(II) complexes, as well as density functional theory (DFT) calculations, shed light on the origin of the enhanced reactivity observed with L1.
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ГОСТ
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Sather A. C. et al. A Fluorinated Ligand Enables Room-Temperature and Regioselective Pd-Catalyzed Fluorination of Aryl Triflates and Bromides // Journal of the American Chemical Society. 2015. Vol. 137. No. 41. pp. 13433-13438.
ГОСТ со всеми авторами (до 50)
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Sather A. C., Lee H. G., De La Rosa V. Y., Yang Y., Müller P., Buchwald S. L. A Fluorinated Ligand Enables Room-Temperature and Regioselective Pd-Catalyzed Fluorination of Aryl Triflates and Bromides // Journal of the American Chemical Society. 2015. Vol. 137. No. 41. pp. 13433-13438.
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TY - JOUR
DO - 10.1021/jacs.5b09308
UR - https://doi.org/10.1021/jacs.5b09308
TI - A Fluorinated Ligand Enables Room-Temperature and Regioselective Pd-Catalyzed Fluorination of Aryl Triflates and Bromides
T2 - Journal of the American Chemical Society
AU - Sather, Aaron C
AU - Lee, Hong Geun
AU - De La Rosa, Valentina Y
AU - Yang, Yang
AU - Müller, Peter
AU - Buchwald, Stephen L.
PY - 2015
DA - 2015/10/06
PB - American Chemical Society (ACS)
SP - 13433-13438
IS - 41
VL - 137
PMID - 26413908
SN - 0002-7863
SN - 1520-5126
ER -
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@article{2015_Sather,
author = {Aaron C Sather and Hong Geun Lee and Valentina Y De La Rosa and Yang Yang and Peter Müller and Stephen L. Buchwald},
title = {A Fluorinated Ligand Enables Room-Temperature and Regioselective Pd-Catalyzed Fluorination of Aryl Triflates and Bromides},
journal = {Journal of the American Chemical Society},
year = {2015},
volume = {137},
publisher = {American Chemical Society (ACS)},
month = {oct},
url = {https://doi.org/10.1021/jacs.5b09308},
number = {41},
pages = {13433--13438},
doi = {10.1021/jacs.5b09308}
}
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MLA
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Sather, Aaron C., et al. “A Fluorinated Ligand Enables Room-Temperature and Regioselective Pd-Catalyzed Fluorination of Aryl Triflates and Bromides.” Journal of the American Chemical Society, vol. 137, no. 41, Oct. 2015, pp. 13433-13438. https://doi.org/10.1021/jacs.5b09308.