Abstract
Phospha-Wittig reagents, RPPMe3 (R = Mes* 2,4,6-tBu3-C6H2;
MesTer 2,6-(2,4,6-Me3C6H2)-C6H3;
DipTer 2,6-(2,6-iPr2C6H3)-C6H3),
can be considered as phosphine-stabilized phosphinidenes. In this study we show
that PMe3 can be displaced by NHCs or NHOs. Interestingly,
phosphinidene-like reactivity results in a subsequent C(sp2)-H
activation of the exocyclic CH2 in NHOs. This concept was further
extended to allyl-apended NHOs, which results in phosphine-substituted allyl
species.
Supplementary materials
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