Issue 36, 2021

Diverse reactivity of carbenes and silylenes towards fluoropyridines

Abstract

The reaction of IDipp with C5F5N led to functionalization of all three carbon atoms of the imidazole ring with HF2 as the counter-anion (1). Reactivity with 2,3,5,6-tetrafluoropyridine gives only C–F bond activation leaving C–H bonds intact (5b). The reaction of SIDipp with C5F5N in the presence of BF3 afforded the ring cleavage product (3). Analogous reactions with silylene led to oxidative addition at the Si(II) center.

Graphical abstract: Diverse reactivity of carbenes and silylenes towards fluoropyridines

Supplementary files

Article information

Article type
Communication
Submitted
15 Marts 2021
Accepted
24 Marts 2021
First published
25 Marts 2021

Chem. Commun., 2021,57, 4428-4431

Diverse reactivity of carbenes and silylenes towards fluoropyridines

G. Kundu, V. S. Ajithkumar, M. K. Bisai, S. Tothadi, T. Das, K. Vanka and S. S. Sen, Chem. Commun., 2021, 57, 4428 DOI: 10.1039/D1CC01401C

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