3-Indolylacyl Radical Cyclizations upon Pyridines and Tetrahydropyridines: Access to Ergoline-Related Indole [cd]-fused Isoquinolines
摘要:
Cyclizations of selenoester-derived 3-indolylacyl radicals, involving the homolytic acylation of pyridines or the addition to double bonds included in tetrahydropyridine rings, have been used to synthesize indole [cd]-fused isoquinolines related to the natural ergoline system.
3-Indolylacyl Radical Cyclizations upon Pyridines and Tetrahydropyridines: Access to Ergoline-Related Indole [<i>cd</i>]-fused Isoquinolines
作者:M.-Lluïsa Bennasar、Tomàs Roca
DOI:10.1021/jo2006279
日期:2011.5.20
Cyclizations of selenoester-derived 3-indolylacyl radicals, involving the homolytic acylation of pyridines or the addition to double bonds included in tetrahydropyridine rings, have been used to synthesize indole [cd]-fused isoquinolines related to the natural ergoline system.