72938-40-0Relevant academic research and scientific papers
ELECTROOXIDATIVE SIMULATION OF STEREOSELECTIVITY IN MICROSOMAL ALLYLIC HYDROXYLATION
Shono, Tatsuya
, p. 91 - 94 (2007/10/02)
A comparison of the stereochemistry of liver microsomal γ-hydroxylation of some cyclic α,β-unsaturated ketones with that of electrochemical γ-acetoxylation of the corresponding dienol esters and with that of peracid oxidation of the dienol esters has been carried out.
Stereospecific Synthesis of Selectively C-7-Acetalized Substituted 4aβ-Methyl-3,4,4a,5,6,8aα-hexahydronaphthalene-1(2H),7(8H)-diones. A Short Total Synthesis of (+/-)-β-Eudesmol, (+/-)-β-Selinene, and (+/-)-β-Dictyopterol
Wijnberg, Joannes B. P. A.,Vader, Jan,Groot, Aede de
, p. 4380 - 4387 (2007/10/02)
An efficient general method has been developed for the synthesis of 4aβ,8α-dimethyl-3,4,4a,5,6,8aα-hexahydronaphthalene-1(2H),7(8H)-dione 7-ethylene acetals 1 and 4aβ-methyl-3,4,4a,5,6,8aα-hexahydronaphthalene-1(2H),7(8H)-dione 7-dimethyl acetals 2, which
