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Trans -geranyl acetone

From tobacco, Schumacher and Heckman have isolated trans-actinidiolide (325), the c/s-isomer having been isolated previously. A synthesis from geranyl-acetone was effected, the essential step being the oxidation of the cyclized compound (326) with permanganate. "" Isoe et al. have extended their successful... [Pg.59]

The stems of E. arvense contain volatile oil with 25 identified compounds. The major constituents include hexahydrofamesyl acetone, geranyl acetone, thymol, and trans-phytol. ... [Pg.367]

Oxidation of 1,5-dienes to c -tetiahydrofurandiols was accomplished with RuO /aq. Na(10 )/acetone-EtOAc thus 2,5-dimethyl-1,5-hexadiene gave tetrahydrofurandiol, geranyl acetate yielded cw-tetrahydrofurandiol, and trans, tra 5-2,6-dimethyl-2,6-octadiene-l,8-diol diacetate (1) gave tetrahydrofuran ketol diacetate (2) (Fig. 3.12 cf. mech. Ch. 1) [174],... [Pg.190]


See other pages where Trans -geranyl acetone is mentioned: [Pg.400]    [Pg.400]    [Pg.5322]    [Pg.190]    [Pg.34]   
See also in sourсe #XX -- [ Pg.984 , Pg.986 ]




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