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Vinyl bromide, Grignard reagent from

This sequence can be used to obtain (3-alkoxy aldehydes with high stereoselectivity from 3-ethoxyallylzinc bromide (4) (6, 607), equation (I).2 The reaction involves almost complete transfer of the stereochemistry of the vinyl Grignard reagent to the aldehyde 5. [Pg.232]

See other pages where Vinyl bromide, Grignard reagent from is mentioned: [Pg.395]    [Pg.239]    [Pg.1288]    [Pg.395]    [Pg.53]    [Pg.168]    [Pg.516]    [Pg.54]    [Pg.34]    [Pg.122]    [Pg.210]    [Pg.612]    [Pg.609]    [Pg.326]    [Pg.345]    [Pg.647]    [Pg.956]    [Pg.114]    [Pg.805]    [Pg.647]    [Pg.956]    [Pg.113]    [Pg.238]    [Pg.388]    [Pg.389]    [Pg.338]    [Pg.91]    [Pg.84]    [Pg.113]    [Pg.145]    [Pg.296]    [Pg.367]    [Pg.614]    [Pg.965]    [Pg.454]    [Pg.211]    [Pg.296]    [Pg.180]    [Pg.1010]    [Pg.95]    [Pg.655]    [Pg.1652]    [Pg.148]    [Pg.175]    [Pg.142]    [Pg.420]    [Pg.296]   
See also in sourсe #XX -- [ Pg.539 ]



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From Grignard reagents

Grignard reagents bromide

Vinyl Grignard

Vinyl Grignard reagents

Vinyl bromide

Vinylic bromides

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