General synthesis for chiral 4-alkyl-4-hydroxycyclohexenones
Some selective transformations of resorcinol-derived cyclohexadienone are reported. Efforts led to a structure reported to display anticancer properties. On the basis of the results, the structures for natural products reported to contain a 4,6-dihydroxy-4-alkyl-cyclohexenone nucleus are corrected.
Hoarau, Christophe,Pettus, Thomas R. R.
p. 2843 - 2846
(2007/10/03)
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