A short, efficient total synthesis of (±) acivicin and (±) bromo-acivicin
- 1 January 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (5) , 487-490
- https://doi.org/10.1016/s0040-4039(00)99918-0
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Synthesis of analogues of the antitumor antibiotic at-125 (acivicin)Tetrahedron, 1983
- Cyanogen chloride N-oxide cycloadditions. A simple, short route to AT-125.Tetrahedron Letters, 1982
- Stereospecific total syntheses of the natural antitumor agent, (.alpha.S, 5S)-.alpha.-amino-3-chloro-4,5-dihydro-5-isoxazoleacetic acid, and its unnatural C-5 epimerJournal of the American Chemical Society, 1981
- Total synthesis of antitumor agent AT-125, (.alpha.S,5S)-.alpha.-amino-3-chloro-4,5-dihydro-5-isoxazoleacetic acidJournal of the American Chemical Society, 1981
- Allylic and propargylic imidic esters in organic synthesisAccounts of Chemical Research, 1980
- Direct synthesis of the antitumor agent -α-amino-3-bromo-4,5-dihydroisoxazole-5-acetic acidTetrahedron Letters, 1980
- Total synthesis of .alpha.-amino-3-chloro-4,5-dihydro-5-isoxazoleacetic acid (AT-125), an antitumor antibioticJournal of the American Chemical Society, 1979
- The isolation, structure, and absolute configuration of U-42,126 a novel antitumor antibioticTetrahedron Letters, 1973
- Imidoester, I. Darstellung von TrichloracetimidsäureesternEuropean Journal of Inorganic Chemistry, 1958
- The Reaction of Sodium Azide with Some Representative EpoxidesJournal of the American Chemical Society, 1954