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Backvall

In 1995, Backvall and van Koten reported tlie brsl example of a catalytic, enan-lioselective S 2 substilulion of a primary allylic acetate in tlie presence of a diiral copper complex [28, 29]. [Pg.272]

An interestmg Diels-Alder reaction using chiral enammes is reported by Backvall, m which a cychc nitronate is formed m good yield and excellent diastereoselecnvity fEq 8 98 ... [Pg.276]


See other pages where Backvall is mentioned: [Pg.290]    [Pg.379]    [Pg.108]    [Pg.109]    [Pg.109]    [Pg.113]    [Pg.113]    [Pg.113]    [Pg.113]    [Pg.117]    [Pg.117]    [Pg.117]    [Pg.117]    [Pg.117]    [Pg.117]    [Pg.117]    [Pg.117]    [Pg.117]    [Pg.117]    [Pg.117]    [Pg.117]    [Pg.118]    [Pg.118]    [Pg.118]    [Pg.118]    [Pg.407]    [Pg.407]    [Pg.407]    [Pg.408]    [Pg.408]    [Pg.412]    [Pg.412]    [Pg.412]    [Pg.449]    [Pg.98]    [Pg.402]    [Pg.138]    [Pg.288]    [Pg.288]    [Pg.53]    [Pg.708]    [Pg.475]    [Pg.888]    [Pg.888]    [Pg.221]    [Pg.221]    [Pg.1118]    [Pg.308]   
See also in sourсe #XX -- [ Pg.253 ]




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Backvall reaction

Backvall system

Backvall’s catalyst

Modem Oxidation Methods. Edited by Jan-Erling Backvall

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