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Germyl anions nucleophilicity

Ph3SiK + Ph2C=0 — Ph6Si2 + PhCH(OH)CH(OH)Ph [20] whereas germyl anions react as nucleophiles (39). [Pg.54]

Nucleophilic attack of the germyl anion toward the P carbon of the cyclic ketone formed a Uthium enolate that coordinated to the germylene regenerating a germyl anion. The organogermanium polymer was stable in aqueous solution and had a > 10 T =40°C, and r =221°C. [Pg.239]

See other pages where Germyl anions nucleophilicity is mentioned: [Pg.450]    [Pg.450]    [Pg.95]    [Pg.546]    [Pg.159]    [Pg.180]    [Pg.726]    [Pg.159]    [Pg.726]   
See also in sourсe #XX -- [ Pg.2 , Pg.4 , Pg.6 , Pg.8 ]



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Anion nucleophilicity

Anionic nucleophiles

Anions germyl

Anions nucleophiles

Germyl

Germyls

Nucleophilic anion

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