Synthesis of hydroxamic acids: as a new catalyst for the deprotection of O-benzyl hydroxamates
- 9 January 1995
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 36 (2) , 197-200
- https://doi.org/10.1016/0040-4039(94)02246-8
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- General method for the synthesis of trishydroxamic acidsTetrahedron Letters, 1992
- Effects of five-membered ring conformation on bioreceptor recognition: identification of 3R-amino-1-hydroxy-4R-methylpyrrolidin-2-one (L-687,414) as a potent glycine/N-methyl-D-aspartate receptor antagonistJournal of the Chemical Society, Chemical Communications, 1990
- The synthesis of acyclonucleoside hydroxamic acids as inhibitors of ribonucleotide reductaseJournal of Medicinal Chemistry, 1989
- Resolution and synthesis of the individual enantiomers of the glycine antagonist 3-amino-1-hydroxypyrrolidin-2-one (HA-966)Journal of the Chemical Society, Chemical Communications, 1989
- Anwendung von N‐Tritylmethionin zur Darstellung von biologisch und synthetisch interessanten HeterocyclenEuropean Journal of Organic Chemistry, 1988
- Artificial siderophores. 2. Syntheses of trihydroxamate analogs of rhodotorulic acid and their biological iron transport capabilities in Escherichia coliJournal of Medicinal Chemistry, 1985
- Complexation of iron by siderophores a review of their solution and structural chemistry and biological functionPublished by Springer Nature ,1984
- Synthesis of Rhodotorulic AcidBulletin of the Chemical Society of Japan, 1972
- The Selective Debenzylation of N-Acyl-O-benzylhydroxylaminesBulletin of the Chemical Society of Japan, 1965
- The synthesis of some N-hydroxyimidesJournal of the Chemical Society, 1955