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Oxyanion-accelerated rearrangements

Oxyaruon-acceleratedrearrangement cf2-vinylcyclobutanol derivatives 8.3.3.13 Oxyanion-accelerated rearrangement cf l-vinylcyclobutanol derivatives... [Pg.999]

In summary then, the oxyanion-accelerated rearrangement of 2-vinylcyclobutanol derivatives is now established as an attractive method for achieving two-carbon ring expansion under relatively mild conditions. In conjunction with the efficient synthetic routes to vinylcyclobutanones outlined in Scheme 21, this version of the VCB rearrangement provides several strategically novel annulation methods for the construction of six-membered carbocycles. ... [Pg.1021]

For other examples of oxyanion-accelerated rearrangements involving 2-vinylcyclobutanol derivatives, see (a)... [Pg.1036]

Oxyanion-accelerated rearrangement cf2-vinylcyclobutanol derivatives 8.33.13 Oxyanion-accelerated rearrangement cfl-vinylcyclobutanol derivatives 8.33.1.4 Azaanion-accelerated vinylcyclobutane rearrangements... [Pg.999]

See other pages where Oxyanion-accelerated rearrangements is mentioned: [Pg.1000]    [Pg.1016]    [Pg.1022]    [Pg.1028]    [Pg.999]    [Pg.1000]    [Pg.1016]    [Pg.1022]    [Pg.1028]   


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1,3-Sigmatropic rearrangements oxyanion-accelerated

Anthracyclinones via oxyanion-accelerated rearrangement

Claisen rearrangements oxyanion-accelerated

Cope rearrangement oxyanion acceleration

Cyclobutanols, 2- rearrangement oxyanion-accelerated

Cyclohexanone, 4-phenylthiosynthesis via oxyanion-accelerated rearrangement

Daunomycinone, 4-demethoxysynthesis via oxyanion-accelerated rearrangement

Oxy-Cope rearrangements oxyanion-accelerated

Oxyanion

Oxyanion-accelerated

Rearrangements acceleration

Tetracyclines via oxyanion-accelerated rearrangement

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