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Allyl hydroximates

A diastereoselective imino [1,2]-Wittig rearrangement of allyl hydroximates provides for the preparation of optically active a-hydroxy oxime ethers when R3 is designed (g) as shown to participate in the reaction (Scheme 5).8... [Pg.432]

The imino [1,2]-Wittig rearrangement was originally reported by Katritzky in 1981, and has been subsequently explored by Uneyama and Naito These transformations involve rearrangements of benzyl or allyl hydroximates to a-hydroxy oximes. An illustrative example involves the... [Pg.234]

See other pages where Allyl hydroximates is mentioned: [Pg.543]    [Pg.543]    [Pg.543]    [Pg.194]    [Pg.195]    [Pg.543]    [Pg.543]    [Pg.543]    [Pg.194]    [Pg.195]   
See also in sourсe #XX -- [ Pg.432 ]



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Hydroximates

Hydroximation

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