Organometallic reactions. Part XIV. The decarboxylation of trialkyltin carbamates by isocyanates and isothiocyanates: a new route to carbodi-imides
- 1 January 1968
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society C: Organic
- p. 2640-2646
- https://doi.org/10.1039/j39680002640
Abstract
Two aspects of organometallic addition reactions are discussed. In the first, one acceptor, A2 B2, displaces another, A1 B1, from the adduct MABX. M–A1–B1–X + A2 B2→ M–A2–B2–X + A1 B1 In the second, exchange of the groups X and A between the addendum MXM and the acceptor AB, is brought about by an addition–elimination sequence. M–X–M + AB → M–A–B–X–M → M–A–M + XB Tributyltin carbamates have been shown to react by the first process with isocyanates to give tributyltin derivatives of ureas. The same carbamates react with isothiocyanates by a combination of the two processes and the reaction provides a new route to carbodi-imides.Keywords
This publication has 0 references indexed in Scilit: