67431-17-8Relevant articles and documents
Synthesis of methoxyfumimycin with 1,2-addition to ketimines
Gross, Patrick J.,Hartmann, Caroline E.,Nieger, Martin,Braese, Stefan
supporting information; experimental part, p. 229 - 232 (2010/04/24)
(Chemical Equation Presented) The synthesis of (±)-methoxyfumimycin, a potential new bacterial peptide deformylase (PDF) inhibitor, is reported. To generate the stereogenic fully substituted carbon, the key step is a 1,2-addition of amethylGrignard reagent to a ketimine. The overall synthetic strategy involves a Dakin oxidation of a vanillin derivative, Friedel-Crafts acylation, Claisen rearrangement, lactonization, and rhodium-catalyzed olefin isomerization.
Selective cleavage of isopropyl aryl ethers by aluminum trichloride
Banwell,Flynn,Stewart
, p. 9139 - 9144 (2007/10/03)
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IMPROVED OXIDATION PROCEDURE WITH AROMATIC PEROXYACIDS
Camps, F.,Coll, J.,Messeguer, A.,Pericas, M.A.
, p. 3895 - 3896 (2007/10/02)
The application of the m-Chloroperbenzoic acid-potassium fluoride system in the Baeyer-Villinger oxidation of aromatic aldehydes and in the epoxidation of olefins has been studied.