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Benzylic anions trimethylsilyl-stabilized

Despite the paucity of data for 9 itself, there now exists a wide range of derivatives in the cyclopropabenzene and -[Z ]naphthalene series that have been expanded upon since a 1987 accountThe preparation of these derivatives can be effected by one of three distinct routes depending upon the particular nature of the compound sought. Each has its limitations and none has provided a parent methylenecycloproparene. The first method depends upon the availability of the cycloproparenyl anion (Section IV.B) which can be intercepted by trimethylsilyl chloride to give silane 93 (R=H). In turn, deprotonation of 93 at the benzylic position affords the stabilized a-silyl anion that gives alkylidene derivatives 94 (R=H) from interaction with an appropriate carbonyl compound in a Peterson olefination (Scheme 12). The reaction sequence can be effected as a one-pot operation... [Pg.730]


See other pages where Benzylic anions trimethylsilyl-stabilized is mentioned: [Pg.213]    [Pg.21]    [Pg.399]    [Pg.730]    [Pg.167]    [Pg.145]    [Pg.944]    [Pg.259]    [Pg.149]   


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Anion stabilization

Anions benzylation

Benzylic anions

Benzylic stability

Benzylic stabilization

Trimethylsilyl anion

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