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Hydroxyalkyl azides asymmetric

Intermolecular Schmidt reactions of alkyl azides and hydroxyalkyl azides with cycloketones in the presence of a Lewis acid, lead to formation of iV-alkyl lactams and A-hydroxyalkyl lactams respectively in good yield. The synthesis of chiral lactams by an asymmetric Schmidt reaction has also been reported. ... [Pg.253]

Variation 4 Asymmetric Schmidt Reaction of Ketones with Hydroxyalkyl Azides (Aube )... [Pg.358]

Scheme 7.15 Asymmetric Schmidt reactions with a monosubstituted hydroxyalkyl azide... Scheme 7.15 Asymmetric Schmidt reactions with a monosubstituted hydroxyalkyl azide...
Rudy H, Cramer KE (1939) Uber den oxydativen Abbau des alloxan-2-dimethylatino anils zu 1-methyl benzimidazol. Chem Ber A 72(4) 728-744 Sahasrabudhe K, Gracias V, Furness K, Smith BT, Katz CE, Reddy DS, Aube J (2003) Asymmetric Schmidt reaction of hydroxyalkyl azides with ketones. J Am Chem Soc 125 (26) 7914-7922. doi 10.1021/ja0348896... [Pg.268]

See other pages where Hydroxyalkyl azides asymmetric is mentioned: [Pg.278]    [Pg.386]    [Pg.670]    [Pg.205]   
See also in sourсe #XX -- [ Pg.204 ]



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