Patrick PALE

Prof. Dr. Patrick PALE

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Research Focus & Metrics

Academic Career Length

33Years (1994-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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21 December 2015 in Catalysis Science & Technology
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SCS. Chassaing
S. Chassaing
VBV. Bénéteau
V. Bénéteau
Patrick PALEPatrick PALE
Patrick PALE
Within the green chemistry context, heterogeneous catalysis is more and more applied to organic synthesis. The well known ‘click chemistry’ and especially its flagship, the copper-catalyzed azide–alkyne cycloaddition reaction (CuAAC), is now catch up by such heterogenisation process and copper ions or metals have been grafted or deposited on or into various solids, such as (bio)polymers, charcoal, silica, zeolites, POM or MOF.

24 June 2021 in Angewandte Chemie International Edition
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RWRobin Weiss
Robin Weiss
EAEmmanuel Aubert
Emmanuel Aubert
Patrick PALEPatrick PALE
Patrick PALE
Victor MamaneVictor Mamane
Victor Mamane

2 September 2016 in Organic & Biomolecular Chemistry
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ABAurélien Blanc
Aurélien Blanc
VBValérie Bénéteau
Valérie Bénéteau
JWJean-Marc Weibel
Jean-Marc Weibel
Patrick PALEPatrick PALE
Patrick PALE
Silver and gold have become incredibly versatile and mild catalysts for numerous transformations, especially in heterocycle synthesis. For the most prominent of them, i.e. furans, silver and gold, with their unique reactivity and mildness, allow numerous possible routes to highly substituted and/or functionalized furans from a large variety of starting materials. Silver and gold catalysis provide thus the most flexible way to this important family of compounds. The present review describes these silver and gold-catalyzed routes, with some emphasis on mechanistic aspects, and proposes a comparison of both the silver and the gold-catalyzed syntheses of furans.

30 October 2023 in Chemistry – A European Journal
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Journal Article
Open access
Patrick PALEPatrick PALE
Patrick PALE
Victor MamaneVictor Mamane
Victor Mamane
Chalcogen bonding (ChB) is the non‐covalent interaction occurring between chalcogen atoms as Lewis acid sites and atoms or groups of atoms able to behave as Lewis bases through their lone pair or π electrons. Analogously to its sister halogen bonding, the high directionality of this interaction was implemented for precise structural organizations in the solid state and in solution. Regarding catalysis, ChB is now accepted as a new mode of activation as demonstrated by the increased number of examples in the last five years. In the family of ChB catalysts, those based on tellurium rapidly appeared to overcome their lighter sulfur and selenium counterparts. In this review, we highlight the Lewis acid properties of tellurium‐based derivatives in solution and summarize the start‐of‐the‐art of their applications in catalysis.

8 March 2010 in European Journal of Organic Chemistry
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ABAurélien Blanc
Aurélien Blanc
AAAurélien Alix
Aurélien Alix
JWJean‐Marc Weibel
Jean‐Marc Weibel
Patrick PALEPatrick PALE
Patrick PALE

11 November 2010 in Organic Letters
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TDThomas Dombray
Thomas Dombray
ABAurélien Blanc
Aurélien Blanc
JWJean-Marc Weibel
Jean-Marc Weibel
Patrick PALEPatrick PALE
Patrick PALE