volume 53 issue 12 pages 3183-3186

Aryl formate as bifunctional reagent: applications in palladium-catalyzed carbonylative coupling reactions using in situ generated CO.

Publication typeJournal Article
Publication date2014-02-14
scimago Q1
wos Q1
SJR5.550
CiteScore27.6
Impact factor16.9
ISSN14337851, 15213773
General Chemistry
Catalysis
Abstract
After decades of development, carbonylation reactions have become one of the most powerful tools in modern organic synthesis. However, the requirement of CO gas limits the applications of such reactions. Reported herein is a versatile and practical protocol for carbonylative reactions which rely on the cooperation of phenyl formate and nonaflate, and the generation of CO in situ. This protocol has a high functionalgroup tolerance and could be applied in carbonylations with C, N, and, O nucleophiles. The corresponding amides, alkynones, furanones, and aryl benzoates were synthesized in good yields.
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GOST Copy
Li H. et al. Aryl formate as bifunctional reagent: applications in palladium-catalyzed carbonylative coupling reactions using in situ generated CO. // Angewandte Chemie - International Edition. 2014. Vol. 53. No. 12. pp. 3183-3186.
GOST all authors (up to 50) Copy
Li H., Neumann H., Beller M., Wu X. Aryl formate as bifunctional reagent: applications in palladium-catalyzed carbonylative coupling reactions using in situ generated CO. // Angewandte Chemie - International Edition. 2014. Vol. 53. No. 12. pp. 3183-3186.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1002/anie.201311198
UR - https://doi.org/10.1002/anie.201311198
TI - Aryl formate as bifunctional reagent: applications in palladium-catalyzed carbonylative coupling reactions using in situ generated CO.
T2 - Angewandte Chemie - International Edition
AU - Li, Haoquan
AU - Neumann, Helfried
AU - Beller, Matthias
AU - Wu, Xiao-Feng
PY - 2014
DA - 2014/02/14
PB - Wiley
SP - 3183-3186
IS - 12
VL - 53
PMID - 24677435
SN - 1433-7851
SN - 1521-3773
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2014_Li,
author = {Haoquan Li and Helfried Neumann and Matthias Beller and Xiao-Feng Wu},
title = {Aryl formate as bifunctional reagent: applications in palladium-catalyzed carbonylative coupling reactions using in situ generated CO.},
journal = {Angewandte Chemie - International Edition},
year = {2014},
volume = {53},
publisher = {Wiley},
month = {feb},
url = {https://doi.org/10.1002/anie.201311198},
number = {12},
pages = {3183--3186},
doi = {10.1002/anie.201311198}
}
MLA
Cite this
MLA Copy
Li, Haoquan, et al. “Aryl formate as bifunctional reagent: applications in palladium-catalyzed carbonylative coupling reactions using in situ generated CO..” Angewandte Chemie - International Edition, vol. 53, no. 12, Feb. 2014, pp. 3183-3186. https://doi.org/10.1002/anie.201311198.