
Journal of Organometallic Chemistry p. 49 - 56 (1985)
Update date:2022-08-30
Topics:
Degueil-Castaing, M.
Maillard, B.
Rahm, A.
High-pressure reaction of tributyltin hydride with several chloroketones (3-chloro-2-butanone, 4-chloro-2-butanone, 5-chloro-2-pentanone, 6-chloro-2-hexanone and 7-chloro-2-heptanone) led to the formation of chloroalkoxytins or cyclic ethers.An ionic mechanism, starting with nucleophilic attack at the carbonyl group, is proposed to explain the formation of the reaction products.
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