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Y-Alkoxyallyltins

In the presence of BF-, etherate, 1 isomerizes to y-alkoxyallyltins, which react with aryl aldehydes to form mainly sy/t-a-glycol monoethers (equation II). How-... [Pg.237]

Chiral acyliminiums were used for the preparation of enantiopure piperidines [267]. Recently, the use of enantio-enriched y-alkoxyallyltins onto chiral acyl iminiums [268] provided a new entry into the synthesis of potential precursors of a-amino-/3-hydroxy adds or aminosugars, with a total control of the stereochemistry. [Pg.226]


See other pages where Y-Alkoxyallyltins is mentioned: [Pg.8]    [Pg.1348]    [Pg.1348]    [Pg.218]    [Pg.225]    [Pg.8]    [Pg.1348]    [Pg.1348]    [Pg.218]    [Pg.225]   
See also in sourсe #XX -- [ Pg.8 ]




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