Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

7,8,15,16-Tetraoxadispiro hexadecane

The Baeyer-Villiger oxidation of cyclohexanone to e-caprolactone using H202 in (CF3)2CHOH proceeds via 7,8,15,16-tetraoxadispiro[5.2.5.2]hexadecane 32. The tetraoxane can be isolated and rearranges to the lactone on treatment with catalytic amounts of 4-TsOH <02 AG(E)4481>. [Pg.378]

See other pages where 7,8,15,16-Tetraoxadispiro hexadecane is mentioned: [Pg.978]    [Pg.112]    [Pg.1171]    [Pg.11]    [Pg.1220]    [Pg.2089]    [Pg.1171]    [Pg.12]    [Pg.1171]    [Pg.2003]    [Pg.12]    [Pg.310]    [Pg.458]    [Pg.500]   
See also in sourсe #XX -- [ Pg.6 ]

See also in sourсe #XX -- [ Pg.378 ]

See also in sourсe #XX -- [ Pg.139 ]



SEARCH



7,8,15,16-tetraoxadispiro

Hexadecan

Hexadecanal

Hexadecane

© 2024 chempedia.info