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Cyclic ketoimides

Cyanooctane, 38 Cyanosilylation, 80-81 Cyanuric chloride, 149 Cyclanones, 351 Cyclic amidines, 78 Cyclic ketoimides, 441 Cyclization, 10... [Pg.371]

Cyclic ketoimides Ozonization of cycUc enamine lactams (1) is a route to medium and macrocyclic ketoimides (2). Yields are lower if m-chloroperbenzoic acid is used. However, this peracid is preferable to ozone for oxidation of N-acetyl enamines of type (3). [Pg.608]

Oxidation of 3,4-dihydropyridin-2-ones (229) (which are easily made by heating primary amines with cycloalkanone propionic esters), and the eneamide (231), with ozone or m-chloroperoxybenzoic acid has led to medium- and macro-cyclic ketoimides (230) and A -acetylketolactams (232) respectively (Scheme 105). ... [Pg.253]

See other pages where Cyclic ketoimides is mentioned: [Pg.152]    [Pg.152]    [Pg.152]    [Pg.152]   
See also in sourсe #XX -- [ Pg.441 ]



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