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Publikováno v:
Chemical Science
A computational and experimental study of the hydrazine-catalyzed ring-opening carbonyl–olefin metathesis of norbornenes is described. Detailed theoretical investigation of the energetic landscape for the full reaction pathway with six different hy
A computational and experimental study of the hydrazine-catalyzed ring-opening carbonyl-olefin metathesis of norbornenes is described. Detailed theoretical investigation of the energetic landscape for the full reaction pathway with six different hydr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0864a086f85e9e9c63b2b9563a05695c
https://doi.org/10.26434/chemrxiv.11385774.v1
https://doi.org/10.26434/chemrxiv.11385774.v1
Autor:
Julien Pomarole, Samuel Beaulieu, Pier Alexandre Champagne, Jean-François Paquin, Yasmine Benhassine, Claude Y. Legault, Marie Ève Thérien
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2013, 15, pp.2210-2213. ⟨10.1021/ol400765a⟩
Organic Letters, 2013, 15, pp.2210-2213. ⟨10.1021/ol400765a⟩
Organic Letters, American Chemical Society, 2013, 15, pp.2210-2213. ⟨10.1021/ol400765a⟩
Organic Letters, 2013, 15, pp.2210-2213. ⟨10.1021/ol400765a⟩
International audience; It was discovered that the presence of water as a cosolvent enables the reaction of activated alkyl fluorides for bimolecular nucleophilic substitution reactions. DFT calculations show that activation proceeds through stabiliz