Two routes of heterocyclization of 2-alkynylanthraquinone-1-diazonium salts. The synthesis of 1 H -naphtho[2,3- h ]cinnoline-4,7,12-trione
作者:Lidiya G Fedenok、Igor I Barabanov、Irena D Ivanchikova
DOI:10.1016/s0040-4020(00)01101-7
日期:2001.2
The possibility of the heterocyclization of vic-alkynylanthraquinonediazonium salts with the formation of a 5- or 6-membered ring, depending on the reaction conditions, is established. The heterocyclization of 2-alkynyl-9,10-anthraquinone-1-diazonium salts to form 1H-naphtho[2,3-h]cinnoline-4,7,12-triones is reported.
根据反应条件,确定了形成5-或6-元环的vic-炔基蒽醌二重氮盐杂环化的可能性。据报道2-炔基-9,10-蒽醌-1-重氮盐的杂环形成1 H-萘[2,3 - h ] cinnoline-4,7,12-三酮。
Convenient method for the synthesis of 2-substituted naphtho[2,3?g]indole-6,11-diones
作者:A. V. Piskunov、M. S. Shvartsberg
DOI:10.1007/bf00962408
日期:1990.6
A convenient one-step method has been developed for the preparation of 2-substituted naphtho[2,3-g]indole-6,11-diones entailing the addition of piperidine to 1-amino-2-acetylenylanthraquinone and subsequent cyclization of the adduct with loss of the amine in the presence of dilute hydrochloric acid.
PISKUNOV, A. V.;SHVARTSBERG, M. S., IZV. AN CCCP. CEP. XIM.,(1990) N, S. 1444-1445
作者:PISKUNOV, A. V.、SHVARTSBERG, M. S.
DOI:——
日期:——
PISKUNOV A. V.; MOROZ A. A.; SHVARTSBERG M. S., IZV. AN CCCP. CEP. XIM.,(1987) N 4, 828-832