Total Synthesis of Gibbilimbols A−D
The Journal of Organic Chemistry2002Vol. 67(7), pp. 2263–2265
Citations Over Time
Abstract
Gibbilimbols A-D (1-4) were synthesized in 32-49% yield over four steps from commercially available starting materials. A copper-catalyzed coupling of 4-methoxyphenylmagnesium bromide with various unsaturated alkyl bromides was the key step in assembling the (long-chain alkyl)phenol skeleton.
Related Papers
- → Bromide residues in potatoes fumigated with methyl bromide(1971)12 cited
- → Polyfluorination of Aryl Alkyl Sulfides by IF5 with Concomitant Migration of the Arylthio Group(2003)19 cited
- → Role of the nature of copper sites in the activity of copper-based catalysts for no conversion(1992)32 cited
- → Thermal properties of silica-based hybrids with different alkyl chains(2016)1 cited
- → Epr study of some copper(II) mononuclear and copper(II)-copper(II)/ copper(II)nickel(II) binuclear complexes(1999)6 cited