作者:Gari Gellerman、Malca Babad、Yoel Kashman
DOI:10.1016/s0040-4039(00)60790-6
日期:1993.3
The symmetrical tetraaza heptacyclic alkaloid eilatin (1) was synthesized in a biomimetic two step reaction from catechol and monotrifluoro kynuramine (6) under oxidative conditions in the first step (aq, EtOH, NaIO3) and basic conditions (ammoniacal MeOH, DMAP) in the second. Two other unsuccessful approaches, one leading to 7-phenylascididemin, are described.