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Homo-Peterson Alkenation. Styrene oxide reacts with lithio-phenylthiobis(trimethylsilyl)methane to afford cyclopropane-containing products (eq 6)7 This reaction is limited, due to the complexity of its mechanism the alkenation reagent must serve to generate both alkenic and carbenic species. For this reason, only styrene oxide and trimethylsilyloxirane undergo this transformation. [Pg.411]

See other pages where Phenylthiobis methane is mentioned: [Pg.411] [Pg.411] [Pg.412] [Pg.772] [Pg.782] [Pg.852]