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Anhydrides Arndt-Eistert homologation

Alder route, was converted into the urethan (25) by a series of unexceptional steps. Arndt-Eistert homologation of (25) provided the carboxylic acid (26) which, upon treatment with acetic anhydride, readily gave the lactam (27). Introduction of a one-carbon unit into the aromatic ring was achieved with chloromethyl methyl ether, and further reductive and hydrolytic modification afforded the amino-alcohol (28). Osmium tetroxide oxidation of (28) yielded the stereoisomeric triols (29) (20%) and (30) (22%) which were separated and oxidized to ( + )-clivonine (31) and (+ )-clividine (32), respectively. [Pg.175]


See other pages where Anhydrides Arndt-Eistert homologation is mentioned: [Pg.393]    [Pg.494]    [Pg.410]    [Pg.339]    [Pg.226]    [Pg.413]    [Pg.199]    [Pg.432]   
See also in sourсe #XX -- [ Pg.346 ]




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