Synthesis of Antitumor Lycorines by Intramolecular Diels−Alder Reaction
摘要:
Pharmacologically interesting lycorines were obtained by a short, efficient method based on an intramolecular Diels-Alder reaction between an alpha-pyrone and an alkyne, followed by loss of CO2 in a retro Diels-Alder reaction. The cyclization precursors (pyrones 9) were obtained in good yields in two or three steps from the corresponding homophthalic acid or anhydride.
A new approach to the synthesis of antitumoralkaloids with the lycorane skeleton
作者:Dolores Pérez、Enrique Guitián、Luis Castedo
DOI:10.1016/s0040-4039(00)74224-9
日期:1992.4
A new approach to the synthesis of lycorane-type alkaloids is described. The key step is intramolecular cycloaddition between an alpha-pyrone and an alkyne.
Synthesis of Antitumor Lycorines by Intramolecular Diels−Alder Reaction
Pharmacologically interesting lycorines were obtained by a short, efficient method based on an intramolecular Diels-Alder reaction between an alpha-pyrone and an alkyne, followed by loss of CO2 in a retro Diels-Alder reaction. The cyclization precursors (pyrones 9) were obtained in good yields in two or three steps from the corresponding homophthalic acid or anhydride.