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Vanadium cyanates

Vacuum manifold system, 51,56 Vanadium oxyacetylacetonate, 50,56 N-Vinylpyrrolidone, cyanation,50,54... [Pg.78]

Avecia, a former part of the Zeneca Group, developed a range of cheap and highly active titanium- or vanadium-based salen catalysts called CACHy catalysts (Scheme 23). They are based on Jacobsen s salen technology, but they are much more reactive and can, for example, be used in concentrations as low as 0.1 mol% in the cyanation of aryl aldehydes. The catalysts show similar reactivity with alkyl aldehydes and ketones and are applicable to the synthesis of the commercially important mandelic acid derivatives. [Pg.264]

In 2004, Katsuki reported vanadium(v)-salen complex 10 catalysed Meerwein-Ponndorf-Verley (MPV) cyanation with excellent enantiocontrol (up to 98% enantiomeric excess) as shown in Scheme 9.4. In this system, the reaction was carried out with 2,4,6-collidine as a cocatalyst at 0 °C and produced adduct 12 with up to 90% enantiomeric excess however, this resulted in low conversion (25% for 24 h). When the reaction was carried out at... [Pg.220]

Scheme 9.4 Enantioselective vanadium salen 10 and salalen 11-catalysed Meerwein-Ponndorf-Verley (MPV) cyanation, reported by Katsuki. ... Scheme 9.4 Enantioselective vanadium salen 10 and salalen 11-catalysed Meerwein-Ponndorf-Verley (MPV) cyanation, reported by Katsuki. ...

See other pages where Vanadium cyanates is mentioned: [Pg.7]    [Pg.1390]    [Pg.653]    [Pg.220]    [Pg.743]    [Pg.264]   
See also in sourсe #XX -- [ Pg.277 ]




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