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Reformatskii synthesis

Mercuric chloride zinc N-Heterocyclics by Reformatskii synthesis... [Pg.196]

The Reformatskii synthesis with trimethylsilyl esters leads directly to / -hydroxy acids after acidic work-up The latter can be converted into olefins via / -lactones with retention of the initial geometry and without double bond isomerization. The synthesis of oxo compounds through 1,3-dithianes has been applied to a convenient preparation of a-keto esters... [Pg.12]

Synthesis of carboxylic acids from ketones via y -hydroxycarboxylic acid fcrf-butyl esters Modified Reformatskii synthesis... [Pg.178]

See other pages where Reformatskii synthesis is mentioned: [Pg.184]    [Pg.159]    [Pg.239]    [Pg.247]    [Pg.176]    [Pg.473]    [Pg.473]    [Pg.216]    [Pg.251]    [Pg.264]    [Pg.267]    [Pg.369]    [Pg.232]    [Pg.290]    [Pg.489]    [Pg.489]    [Pg.330]    [Pg.330]    [Pg.352]    [Pg.353]    [Pg.598]    [Pg.598]    [Pg.598]    [Pg.238]    [Pg.242]    [Pg.242]    [Pg.246]    [Pg.282]   
See also in sourсe #XX -- [ Pg.26 , Pg.673 ]

See also in sourсe #XX -- [ Pg.26 ]



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Reformatskii synthesi

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