Synthesis of 9,10,12,13,14,14a-hexahydrodibenzo[<i>f,h</i>]pyrrolo-[2,1-<i>a</i>]isoquinoline
作者:Rodolfo Copado C.、Mercedes T. Grande G.、Gregorio G. Trigo、Mónica M. Söllhuber K
DOI:10.1002/jhet.5570230259
日期:1986.3
The synthesis of 9,10,12,13,14,14a-hexahydrodibenzo[f,h]pyrrolo[2,1-a]isoquinoline 6 has been accomplished by a sequence involving as a key step the Friedel-Crafts intramolecular acylation of the amino acid 9 to the corresponding pentacyclic aminoketone 10. Compounds 7, 11 and 12 showed a significant protein synthesis inhibitory effect.
9,10,12,13,14,14a-六氢二苯并[ f,h ]吡咯并[ 2,1- a ]异喹啉6的合成已通过一系列的步骤完成,该步骤涉及作为关键步骤的Friedel-Crafts分子内酰化反应。氨基酸9为相应的五环氨基酮10。化合物7、11和12显示出显着的蛋白质合成抑制作用。