In this paper,we report a full account of the synthesis of dimeric hexahydropyrroloindole alkaloids and its analogues.The key feature of our new strategy is the novel catalytic copper(10%)mediated intramolecular aryla...In this paper,we report a full account of the synthesis of dimeric hexahydropyrroloindole alkaloids and its analogues.The key feature of our new strategy is the novel catalytic copper(10%)mediated intramolecular arylations of o-haloanilides followed by intermolecular oxidative dimerization of the resulting oxindoles in one pot.This sequential reaction leads to the key intermediates for the synthesis of(+)-chimonanthine,(+)-folicanthine,(-)-calycanthine and(-)-ditryptophenaline.Graphical Abstract In the presence of catalytic amount of cuprous iodide(10%),an intramolecular arylation of ohaloanilides followed by an intermolecular oxidative dimerization of the resulting oxindoles leads to a commonintermediate for the synthesis of(+)-chimonanthine,(+)-folicanthine and(-)-calycanthine.Based on this cascade sequence,we also developed a flexible strategy towards the asymmetric syntheses of dimeric HPI alkaloids(-)-ditryptophenaline and its analogues.展开更多
基金This work was supported by Grants from Natural Science Foundation of China(20925205 and 21332007)the Program for Changjiang Scholars and Innovative Research Team in University(IRT13095)+1 种基金Yunnan Provincial Science and Technology Department(2010GA014)the Program for Yunling Scholars.Dr.Xiaonian Li of the Kunming Institute of Botany is gratefully acknowledged for X-ray crystallographic analysis of compound 23.CCDC 1409209(23).
文摘In this paper,we report a full account of the synthesis of dimeric hexahydropyrroloindole alkaloids and its analogues.The key feature of our new strategy is the novel catalytic copper(10%)mediated intramolecular arylations of o-haloanilides followed by intermolecular oxidative dimerization of the resulting oxindoles in one pot.This sequential reaction leads to the key intermediates for the synthesis of(+)-chimonanthine,(+)-folicanthine,(-)-calycanthine and(-)-ditryptophenaline.Graphical Abstract In the presence of catalytic amount of cuprous iodide(10%),an intramolecular arylation of ohaloanilides followed by an intermolecular oxidative dimerization of the resulting oxindoles leads to a commonintermediate for the synthesis of(+)-chimonanthine,(+)-folicanthine and(-)-calycanthine.Based on this cascade sequence,we also developed a flexible strategy towards the asymmetric syntheses of dimeric HPI alkaloids(-)-ditryptophenaline and its analogues.
