Trimethylsilylcyanid als Umpolungsreagens,VI. Anionische 1,4- O→C-Silylgruppen-Umlagerung

Trimethylsilyl Cyanide — A Reagent for Umpolung, VI. Anionic 1,4-O→C-Silyl Group Rearrangement The adducts 6 from substituted acroleins 5a – f and trimethylsilyl cyanide form the anions 6 _A on deprotonation at −78°C, which are silylated by trimethylsilyl chloride to 7 or (and) 8 in positions 3 or (and) 1. On warming up to room temperature, 6a _A and 6b _A undergo smoothly 1,4-O→C-silyl group rearrangements to form 13a _A and 13b _A which can be trapped by silylation. 6c – d _A decompose on warming up. Triethylsilyl instead of trimethylsilyl groups decelerate the rearrangement appreciably. Structure and configuration of the different products are determined.