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Dimethyl methylthiosulfonium

Carbamate glycosyl donors are another useful class of compounds, which pre sent significant variability in chemical structures (Scheme 3.24). In an early example by Kunz and Zimmer, the N-allyl carbamate donors were used in a remote activation protocol to furnish pyranoside and furanoside products. In this reaction, the N-allyl carbamate donor 146 is activated with dimethyl methylthiosulfonium... [Pg.144]

Acyloxyselenylation Benzeneselenenyl halides, 26 N-Phenylselenophthalimide, 245 Acyloxysulfenylation Dimethyl(methylthiosulfonium) tetra-fluoroborate, 121... [Pg.353]

Cross-coupling of alkyl + alkynyl groups Potassium hydroxide-18-Crown-6, 258 Cross-coupling of alkyl + allyl groups Crotyltrimethylsilane, 86 Dimethyl(methylthiosulfonium) tetra-fluoroborate, 121 Lithium, 157... [Pg.362]

From unsaturated carboxylic acids Benzeneselenenyl halides, 26 Dimethyl(methylthiosulfonium) tetrafluoroborate, 121 By other methods... [Pg.394]

See other pages where Dimethyl methylthiosulfonium is mentioned: [Pg.396]    [Pg.395]    [Pg.63]    [Pg.396]    [Pg.395]    [Pg.63]   


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