Desilylation of either α-silyl sulphides or silyl dihydrothiopyrans (easily obtained from silyl thiones as primary adducts), when performed in the presence of carbon electrophiles (aldehydes or ketones), offers an easy entry to carbofunctionalised products. © 1991.
Bonini B.F., Masiero S., Mazzanti G., Zani P. (1991). Synthetic usefulness of silyl thioketones: Functionalization of their primary adducts through desilylation and trapping by carbon electrophiles. TETRAHEDRON LETTERS, 32(6), 815-818 [10.1016/S0040-4039(00)74895-7].
Synthetic usefulness of silyl thioketones: Functionalization of their primary adducts through desilylation and trapping by carbon electrophiles
Bonini B. F.;Masiero S.;Mazzanti G.;Zani P.
1991
Abstract
Desilylation of either α-silyl sulphides or silyl dihydrothiopyrans (easily obtained from silyl thiones as primary adducts), when performed in the presence of carbon electrophiles (aldehydes or ketones), offers an easy entry to carbofunctionalised products. © 1991.File in questo prodotto:
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