99573-14-5Relevant academic research and scientific papers
Inverse Electron Demand Diels-Alder Reactions of Heterocyclic Aza Dienes. Studies on the Total Synthesis of Lavendamycin: Investigative Studies on the Preparation of the CDE β-Carboline Ring System and AB Quinoline-5,8-quinone Ring System
Boger, Dale L.,Duff, Steven R.,Panek, James S.,Yasuda, Masami
, p. 5782 - 5789 (2007/10/02)
The investigation and utilization of the inverse electron demand cycloaddition of 3,5,6-tris(ethoxycarbonyl)-1,2,4-triazine with electron-rich olefins and the subsequent implementation of a palladium(0)-mediated β-carboline synthesis for the preparation of the CDE ring system of lavendamycin are detailed.Studies on the introduction and preparation of the 7-aminoquinoline-5,8-quinone AB ring system of lavendamycin are described.
PALLADIUM (0) MEDIATED β-CARBOLINE SYNTHESIS: PREPARATION OF THE CDE RING SYSTEM OF LAVENDAMYCIN
Boger, Dale L.,Panek, James S.
, p. 3175 - 3178 (2007/10/02)
A five-step approach to the preparation of the β-carboline CDE ring system of lavendamycin is detailed and is based on: (1) thermal cycloaddition of 3,5,6-tricarbomethoxy-1,2,4-triazine with the pyrrolidine enamine of o-bromopropiophenone followed by (2) implementation of a newly developed palladium (0) mediated β-carboline synthesis.
