作者: M.-Lluïsa Bennasar , Bernat Vidal , Joan Bosch
DOI: 10.1039/CC9960002755
关键词:
摘要: A general route to silicine-methuenine alkaloids, exemplified by the synthesis of 6-oxo-16-episilicine, involving nucleophilic addition an acetylindole enolate pyridinium salt 2, methoxycarbonylation resulting 1,4-dihydropyridine, controlled catalytic hydrogenation, cyclization on indole 3-position and further functional group manipulations, is reported.