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Azaacetals reduction

Reduction of Acetals, Azaacetals and Thioacetals to Ethers. Brewster, J. H. In Comprehensive Organic Synthesis TVost, B. M., Fleming, I., Eds. Pergamon Press Oxford, 1991 Vol. 8, p 211. [Pg.118]

This pattern of cleavage is also followed when the azaacetal is acyclic (equation 29) and even when the nitrogen atom is part of a three-membered ring (equation 30). Tetrahydropyranylamines are reduced to E-hydroxypentylamines by hydrogenation overNi or reduction with LAH (equation 31). °... [Pg.228]

See other pages where Azaacetals reduction is mentioned: [Pg.211]    [Pg.213]    [Pg.215]    [Pg.217]    [Pg.219]    [Pg.221]    [Pg.223]    [Pg.225]    [Pg.227]    [Pg.229]    [Pg.231]    [Pg.233]    [Pg.998]   
See also in sourсe #XX -- [ Pg.228 ]

See also in sourсe #XX -- [ Pg.8 , Pg.228 ]

See also in sourсe #XX -- [ Pg.8 , Pg.228 ]



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Azaacetals

Reduction acetals, azaacetals and thioacetals

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