Selective Hydroxy Group Protection of Gallic Acid
- 1 July 1996
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 26 (13) , 2479-2486
- https://doi.org/10.1080/00397919608004560
Abstract
An efficient procedure allowing selective differentiation of the 4-hydroxy group of methyl gallate was reported.Keywords
This publication has 10 references indexed in Scilit:
- Asymmetric synthesis of (2S,3R) β-(4-F-3-NO2) phenyl serine, D-(R)-4-methoxy-3,5-bistbutyldimethylsiloxy phenylglycine and their assemblage to C-O-D ring of vancomycinTetrahedron Letters, 1995
- Reductive deprotection of aryl allyl ethers with Pd(Ph3)4/NaBH4Tetrahedron Letters, 1994
- A SN Ar based facile synthesis of triaryl diethers, degradation products of vancomycin and related glycopeptide antibioticsTetrahedron Letters, 1993
- Structure-activity relationships of vancomycin-type glycopeptide antibiotics.The Journal of Antibiotics, 1993
- An Efficient Procedure for the Regioselective Monoprotection of 1,2-DiolsTetrahedron, 1992
- Studies on the synthesis of aryl ethers using arene-manganese chemistryThe Journal of Organic Chemistry, 1991
- Structure of ternatin A1, the largest ternatin in the major blue anthocyanins fromTetrahedron Letters, 1990
- Constituents of Cannabis sativa, XXV. Isolation of Two New Dihydrostilbenes from a Panamanian VariantJournal of Natural Products, 1984
- Structure revision of the antibiotic vancomycin. Use of nuclear Overhauser effect difference spectroscopyJournal of the American Chemical Society, 1981
- Synthesis of thomasic acidTetrahedron, 1973