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, 61 (6), pii: e02397-16, (2017).

Commercialization of 2,3-DCP (2011)

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Commercialization 2,5 DB3MP (2013)

All reactions were monitored by TLC analysis containing GF254 and revealed in vanillin. Melting points were determined in an open capillary tube and performed on a PFM II BioSan apparatus. Elemental analyses were carried out on an EA 1110 CHNS-O analyzer from Carlo Erba Instruments. The infrared spectra were recorded on an IFS66 Bruker spectrophotometer using KBr discs. 1H and 13C NMR were obtained on Varian Unity Plus-300 and Varian UNMRS 400MHz spectrometer using CDCl3 or DMSO-d6 as a solvent. The polarimeter used was the Krüss, of 10cm path length and concentration of the solution in g/100mL. The purity of the compounds was attested on an HPLC-DAD Shimadzu Prominence Model.

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h.; Selkti, M.; Lavergne, J.-P.; Compain, P., Synthesis of a novel heterocyclic ring system by way of highly regio- and chemoselective 1,3-dipolar cycloaddition of nitrilimines to 1,3,4-benzotriazepin-5-one derivatives.

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J.; Buerkstuemmer, E.; Linclau, B., Short Synthesis of Enantiopure 2-Symmetric 1,2:4,5-Diepoxypentane and "Pseudo"-2-Symmetric 3-Azido-1,2:4,5-diepoxypentane from Arabitol.

V.; Van der Eycken, E., A microwave-assisted click chemistry synthesis of 1,4-disubstituted 1,2,3-triazoles via a copper(I)-catalyzed three-component reaction.

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Fokin, Polytriazoles as Copper(I)-Stabilizing Ligands in Catalysis,

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Isolation of a Copper(I) Triazolide: a "Click" Intermediate.

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Synthesis and Supramolecular Structures of N3P3(N(Me)N=CHC6F5)6, -N3P3(C12H8O2)(N(Me)N=CHC6F5)4, and -N3P3(C12H8O2)2(N(Me)N=CHC6F5)2.

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