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Nucleophilic addition reactions phosphonium ylide synthesis

The employment of phosphorus-stabilized carbon nucleophiles for alkene synthesis was initiated by the discovery of the Wittig reaction [10], which provides a convenient method for the preparation of a wide variety of polysubstituted alkenes with complete positional selectivity and generally high levels of geometrical control. Moreover, the phosphonium ylides used in the Wittig reaction are readily formed by the addition of suitable bases to the corresponding phosphonium salts, which are commonly prepared by treating alkyl halides with phosphines. [Pg.199]


See other pages where Nucleophilic addition reactions phosphonium ylide synthesis is mentioned: [Pg.44]    [Pg.20]    [Pg.1484]    [Pg.83]    [Pg.30]    [Pg.211]    [Pg.661]    [Pg.176]    [Pg.84]    [Pg.176]   
See also in sourсe #XX -- [ Pg.6 , Pg.194 ]




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Addition reactions nucleophilic

Addition synthesis

Additive synthesis

Nucleophile addition reactions

Nucleophiles addition reactions

Phosphonium ylide

Phosphonium ylides addition reactions

Phosphonium ylides reactions

Phosphonium ylides synthesis

Synthesis addition reactions

Ylide reaction

Ylide synthesis

Ylides addition

Ylides reaction

Ylides synthesis

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