Acylation of lycoctonine: semi-synthesis of inuline, delsemine analogues and methyllycaconitine
…, DJ Hardick, T Lewis, MG Rowan, S Wonnacott…
文献索引：Blagbrough, Ian S.; Coates, Philippa A.; Hardick, David J.; Lewis, Terence; Rowan, Michael G.; Wonnacott, Susan; Potter, Barry V. L. Tetrahedron Letters, 1994 , vol. 35, # 46 p. 8705 - 8708
Abstract Lycoctonine has been acylated to afford sequentially inuline, delsemine analogues and methyllycaconitine using isatoic anhydride followed by S-(−)-methylsuccinic anhydride. This protocol is a rapid, facile method for the regiospecific introduction of the anthranilate ester moiety found in potent nicotinic acetylcholine receptor antagonists.
