Structure and Reactivity of Indolylmethylium Ions: Scope and Limitations in Synthetic Applications

Elsa Follet, Guillaume Berionni, Peter Mayer, Herbert Mayr

Résultats de recherche: Contribution à un journal/une revueArticle

Résumé

Eight substituted aryl(indol-3-yl)methylium tetrafluoroborates 3(a-h)-BF4 and three bis(indol-3-yl)methylium tetrafluoroborates 3(i-k)-BF4 have been synthesized and characterized by NMR spectroscopy and X-ray crystallography. Their reactions with π-nucleophiles 8(a-j) (silylated enol ethers and ketene acetals) were studied kinetically using photometric monitoring at 20 °C. The resulting second-order rate constants were found to follow the correlation log k(20 °C) = sN(N + E), in which nucleophiles are characterized by the two solvent-dependent parameters N and sN, and electrophiles are characterized by one parameter, E. From the previously reported N and sN parameters of the employed nucleophiles and the measured rate constants, the electrophilicities of the indol-3-ylmethylium ions 3(a-k) were derived and used to predict potential nucleophilic reaction partners. A discrepancy between published rate constants for the reactions of morpholine and piperidine with the (2-methylindol-3-yl)phenylmethylium ion 3h and those calculated from E, N, and sN was analyzed and demonstrated to be due to a mistake of the value reported in the literature.

langue originaleAnglais
Pages (de - à)8643-8656
Nombre de pages14
journalJournal of Organic Chemistry
Volume80
Numéro de publication17
Les DOIs
Etat de la publicationPublié - 28 juil. 2015
Modification externeOui

    Empreinte digitale

Contient cette citation