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New fluorinated catalysts for olefin metathesis

Salekh Masoud Masoud 1, 2
Salekh Masoud Masoud
, 
Arthur Karenovich Mailyan 1, 3
Arthur Karenovich Mailyan
, 
Aleksandr Sergeevich Peregudov 1
Aleksandr Sergeevich Peregudov
, 
Christian Bruneau 2
Christian Bruneau
, 
Sergey Nikolaevich Osipov 1
Sergey Nikolaevich Osipov
10.1016/j.mencom.2016.11.004
Published 2016-10-27
Communication , Volume 26, Issue 6, 474-476
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Masoud S. M. et al. New fluorinated catalysts for olefin metathesis // Mendeleev Communications. 2016. Vol. 26. No. 6. pp. 474-476.
GOST all authors (up to 50) Copy
Masoud S. M., Mailyan A. K., Peregudov A. S., Bruneau C., Osipov S. N. New fluorinated catalysts for olefin metathesis // Mendeleev Communications. 2016. Vol. 26. No. 6. pp. 474-476.
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TY - JOUR
DO - 10.1016/j.mencom.2016.11.004
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.11.004
TI - New fluorinated catalysts for olefin metathesis
T2 - Mendeleev Communications
AU - Masoud, Salekh Masoud
AU - Mailyan, Arthur Karenovich
AU - Peregudov, Aleksandr Sergeevich
AU - Bruneau, Christian
AU - Osipov, Sergey Nikolaevich
PY - 2016
DA - 2016/10/27
PB - Mendeleev Communications
SP - 474-476
IS - 6
VL - 26
ER -
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@article{2016_Masoud,
author = {Salekh Masoud Masoud and Arthur Karenovich Mailyan and Aleksandr Sergeevich Peregudov and Christian Bruneau and Sergey Nikolaevich Osipov},
title = {New fluorinated catalysts for olefin metathesis},
journal = {Mendeleev Communications},
year = {2016},
volume = {26},
publisher = {Mendeleev Communications},
month = {Oct},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.11.004},
number = {6},
pages = {474--476},
doi = {10.1016/j.mencom.2016.11.004}
}
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Masoud, Salekh Masoud, et al. “New fluorinated catalysts for olefin metathesis.” Mendeleev Communications, vol. 26, no. 6, Oct. 2016, pp. 474-476. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2016.11.004.

Abstract

New olefin metathesis catalysts, analogues of Grubbs II ones, bearing hexafluoroisopropylmethoxy groups in NHC ligand, provide high conversions in model ring closing metathesis of diallylmalonate and cross metathesis of allylbenzene with 1,3-diacetoxybut-2-ene.

References

3.
10.1016/j.mencom.2016.11.004_sbref0005c
Connon
2004
4.
10.1016/j.mencom.2016.11.004_sbref0005d
Olefin Metathesis Theory and Practice, 2014
5.
Ruthenium-Based Heterocyclic Carbene-Coordinated Olefin Metathesis Catalysts
Vougioukalakis G.C., Grubbs R.H.
Chemical Reviews, 2009
6.
10.1016/j.mencom.2016.11.004_sbref0010b
Fischmeister
Metathesis Chemistry: From Nanostructure Design to Synthesis of Advanced Materials, 2007
8.
The ROMP toolbox upgraded
Leitgeb A., Wappel J., Slugovc C.
Polymer, 2010
9.
Ruthenium-based olefin metathesis catalysts bearing N-heterocyclic carbene ligands.
Samojłowicz C., Bieniek M., Grela K.
Chemical Reviews, 2009
10.
Metathesis Reactions: Recent Trends and Challenges
Deraedt C., d'Halluin M., Astruc D.
European Journal of Inorganic Chemistry, 2013
11.
10.1016/j.mencom.2016.11.004_sbref0020a
Kirsch
Modern Fluoroorganic Chemistry, 2004
15.
10.1016/j.mencom.2016.11.004_sbref0025a
Uneyama
Organofluorine Chemistry, 2006
16.
Assessing the Bioisosterism of the Trifluoromethyl Group with a Protease Probe
Jagodzinska M., Huguenot F., Candiani G., Zanda M.
ChemMedChem, 2009
18.
Crystal Structure and Computational Investigation of an Analogue of Grubbs’ Second Generation Catalyst with a Fluorous Phosphine
Tuba R., Brothers E.N., Reibenspies J.H., Bazzi H.S., Gladysz J.A.
Inorganic Chemistry, 2012
19.
Synthesis and RCM Reactions Using a Recyclable Grubbs−Hoveyda Metathesis Catalyst Activated by a Light Fluorous Tag
Matsugi M., Kobayashi Y., Suzumura N., Tsuchiya Y., Shioiri T.
Journal of Organic Chemistry, 2010
20.
Experimental and theoretical study of Hoveyda–Grubbs catalysts modified by perfluorohexyl ponytail in the alkoxybenzylidene ligand
Kvíčala J., Schindler M., Kelbichová V., Babuněk M., Rybáčková M., Kvíčalová M., Cvačka J., Březinová A.
Journal of Fluorine Chemistry, 2013
24.
Novel Ruthenium-Based Metathesis Catalysts Containing Electron- Withdrawing Ligands:  Synthesis, Immobilization, and Reactivity
Halbach T.S., Mix S., Fischer D., Maechling S., Krause J.O., Sievers C., Blechert S., Nuyken O., Buchmeiser M.R.
Journal of Organic Chemistry, 2005
25.
Electronic Effects of the Anionic Ligand in Ruthenium-Catalyzed Olefin Metathesis
Monfette S., Camm K.D., Gorelsky S.I., Fogg D.E.
Organometallics, 2009
26.
Olefin Metathesis Reactions with Fluorinated Substrates, Catalysts, and Solvents
Fustero S., Simón-Fuentes A., Barrio P., Haufe G.
Chemical Reviews, 2014
27.
10.1016/j.mencom.2016.11.004_sbref0045b
Siano
Cent. Eur. J. Chem., 2011
28.
Comparative Investigation of Ruthenium-Based Metathesis Catalysts Bearing N-Heterocyclic Carbene (NHC) Ligands
Fürstner A., Ackermann L., Gabor B., Goddard R., Lehmann C.W., Mynott R., Stelzer F., Thiel O.R.
Chemistry - A European Journal, 2001
29.
Rate Acceleration in Olefin Metathesis through a Fluorine−Ruthenium Interaction
Ritter T., Day M.W., Grubbs R.H.
Journal of the American Chemical Society, 2006
30.
Ruthenium-Olefin Complexes: Effect of Ligand Variation upon Geometry
Anderson D., O'Leary D., Grubbs R.
Chemistry - A European Journal, 2008
31.
Metathesis Catalysts with Fluorinated Unsymmetrical NHC Ligands
Masoud S.M., Mailyan A.K., Dorcet V., Roisnel T., Dixneuf P.H., Bruneau C., Osipov S.N.
Organometallics, 2015
32.
Perhalo Ketones. VI. Aromatic Amino Derivatives of the Perhaloacetones
Gilbert E.E., Jones E.S., Sibilia J.P.
Journal of Organic Chemistry, 1965
33.
Reactions of highly electrophilic polyfluorocarbonyl compounds with primary arylamines
Chkanikov N.D., Sviridov V.D., Zelenin A.E., Galakhov M.V., Kolomiets A.F., Fokin A.V.
Russian Chemical Bulletin, 1990
34.
A Series of Well‐Defined Metathesis Catalysts–Synthesis of [RuCl2(CHR′)(PR3)2] and Its Reactions
Schwab P., France M.B., Ziller J.W., Grubbs R.H.
Angewandte Chemie International Edition in English, 1995
35.
A Recyclable Ru-Based Metathesis Catalyst
Kingsbury J.S., Harrity J.P., Bonitatebus P.J., Hoveyda A.H.
Journal of the American Chemical Society, 1999
36.
A Standard System of Characterization for Olefin Metathesis Catalysts
Ritter T., Hejl A., Wenzel A.G., Funk T.W., Grubbs R.H.
Organometallics, 2006
38.
Efficient and Recyclable Monomeric and Dendritic Ru-Based Metathesis Catalysts
Garber S.B., Kingsbury J.S., Gray B.L., Hoveyda A.H.
Journal of the American Chemical Society, 2000