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Cyclogeranic acid

Cyclogeranic acid, 24 570 Cycloheptaamylose, 4 714 Cycloheptylamine, physical properties of, 2 498t... [Pg.242]

One synthetic route to the damascones starts with an appropriate cyclogeranic acid derivative (halide, ester, etc.). This is reacted with an allyl magnesium halide to give 2,6,6-trimethylcyclohexenyl diallyl carbinol, which on pyrolysis yields the desired l-(2,6,6-trimethylcyclohexenyl)-3-buten-l-one. Damascone is obtained by rearrangement of the double bond in the side-chain [98]. [Pg.67]

Thermal decomposition of the oligomeric ester produced a- and /3-cyclogeranic acids in 47% and 30% yields, respectively. Other preparative methods for these acids is described (1). [Pg.19]

Cyclohexene-1-carboxylic acid, 2,6,6-trimethyl- cyclogeranic acid)... [Pg.333]

A -Cyclogeranic Acid ( -Cyclogeranic acid, 1 3 Z-irimdhylcyclohexene-2-oarboxylic acid)... [Pg.600]

A -Cydogeranic Acid (a-Cyclogeranic acid, 1.-5 54rimeBiylcyclohexene-6.carboxylic add)... [Pg.600]

See other pages where Cyclogeranic acid is mentioned: [Pg.95]    [Pg.47]    [Pg.219]    [Pg.198]    [Pg.198]    [Pg.47]    [Pg.17]    [Pg.966]    [Pg.95]    [Pg.47]    [Pg.219]    [Pg.198]    [Pg.198]    [Pg.47]    [Pg.17]    [Pg.966]    [Pg.283]    [Pg.47]    [Pg.392]    [Pg.348]   
See also in sourсe #XX -- [ Pg.351 ]



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Cyclogeranate

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