Affiliation:
1. Department of Chemistry University of Oxford Chemistry Research Laboratory 12 Mansfield Rd. Oxford OX1 3TA UK
2. Department of Chemistry Indiana University 800 E. Kirkwood Ave. Bloomington IN., 47405 USA
Abstract
AbstractWe describe the facile synthesis of [(Me3Si)2CH]2E=PMes* (E=Ge, Sn) from the reaction of the tetrylenes with the phospha‐Wittig reagent, Me3P−PMes*. Their reactivity towards a range of substrates with protic and hydridic E−H bonds (E=N, O, Si) is described. In addition to hydroelementation reactions of the E=P bonds, we show that these compounds, particularly [(Me3Si)2CH]2Sn=PMes*, also act as base‐stabilized phosphinidenes, allowing phosphinidene transfer to other nucleophiles.
Funder
Engineering and Physical Sciences Research Council
Subject
General Chemistry,Catalysis,Organic Chemistry
Cited by
4 articles.
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