Tetrahedron Letters p. 7017 - 7018 (1996)
Update date:2022-08-22
Topics:
Lefevre, Valerie
Dat, Yves
Ripoll, Jean-Louis
Dimethylsilanethione was cleanly generated, under flash vacuum thermolysis conditions, by retro-ene cleavage of propargylthiodimethylsilane. The cothermolysis of this latter and ketene dimer led in 60% yield to an only [2 + 2] cycloadduct, 2,2-dimethyl-4-methylene-2-sila-3-thiaoxetane, which in turn can be cleaved at higher temperature to give hexamethylcyclotrisiloxane.
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