Valentin Magne
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Explore the profile of Valentin Magne including associated specialties, affiliations and a list of published articles.
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9
Citations
53
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Recent Articles
1.
Magne V, Cretoiu I, Mallet-Ladeira S, Maerten E, Madec D
Molecules
. 2024 Oct;
29(20).
PMID: 39459178
Tetrahydro-4-thiopyran-4-one 1-oxide and sulfinyl-di--butylpropionate were reported as sources of bis-sulfenate anion and applied in a double pallado-catalyzed cross-coupling reaction for the synthesis of symmetrical biarylsulfoxides, tolerating a large array of...
2.
Magne V, Lenk R, Mallet-Ladeira S, Maerten E, Madec D
Molecules
. 2024 Jul;
29(14).
PMID: 39064910
Pentafluorophenyl copper(I)-biarylsulfoxide complexes, existing as [Cu(CF)]L, both in solution and in the solid state, were prepared and thoroughly characterized. Subsequently, the photochemistry of the complexes was explored, showing inherent photoreactivity...
3.
Ma Q, Buchon L, Magne V, Graff B, Morlet-Savary F, Xu Y, et al.
Macromol Rapid Commun
. 2022 May;
43(19):e2200314.
PMID: 35526219
In both organic and polymer synthesis, photochemistry of charge transfer complexes (CTCs) is considered as a powerful approach to expand visible-light-driven radical chemistry reaction. One reports herein on the development...
4.
Beddoe R, Andrews K, Magne V, Cuthbertson J, Saska J, Shannon-Little A, et al.
Science
. 2019 Aug;
365(6456):910-914.
PMID: 31467220
Nucleophilic substitution reactions of alcohols are among the most fundamental and strategically important transformations in organic chemistry. For over half a century, these reactions have been achieved by using stoichiometric,...
5.
Magne V, Ball L
Chemistry
. 2019 May;
25(37):8903-8910.
PMID: 31067346
Thiophenols are versatile synthetic intermediates whose practical appeal is marred by their air sensitivity, toxicity and extreme malodor. Herein we report an efficient catalytic method for the preparation of S-aryl...
6.
Garnier T, Danel M, Magne V, Pujol A, Beneteau V, Pale P, et al.
J Org Chem
. 2018 May;
83(12):6408-6422.
PMID: 29790337
The copper(I)-doped zeolite Cu-USY proved to be a versatile, efficient, and recyclable catalyst for various Ullmann-type coupling reactions. Easy to prepare and cheap, this catalytic material enables the arylation and...
7.
Magne V, Lorton C, Marinetti A, Guinchard X, Voituriez A
Org Lett
. 2017 Sep;
19(18):4794-4797.
PMID: 28876069
(R)-(-)-Rhazinilam has been synthesized in nine steps and 20% overall yield. The key steps involve two metal-catalyzed processes: the enantioselective gold(I)-catalyzed cycloisomerization of an allene-functionalized pyrrole and the palladium-catalyzed hydrocarboxylation...
8.
Aillard P, Dova D, Magne V, Retailleau P, Cauteruccio S, Licandro E, et al.
Chem Commun (Camb)
. 2016 Aug;
52(73):10984-7.
PMID: 27534612
Substituted phosphathiahelicenes have been prepared via a straightforward two-step procedure involving the regioselective bromination of a preformed helical scaffold, followed by palladium catalyzed coupling reactions. The new helicenes have been...
9.
Magne V, Garnier T, Danel M, Pale P, Chassaing S
Org Lett
. 2015 Sep;
17(18):4494-7.
PMID: 26322645
The catalytic potential of copper(I)-exchanged zeolites was evaluated in the Ullmann-type synthesis of diaryl ethers. Among four investigated zeolites (i.e., USY, MOR, β, and ZSM5), Cu(I)-USY was the best catalyst...