Oxidative coupling of 4a,9-diaza-1,2,4a,9a-tetrahydrofluorenes. 1. Synthesis of mononuclear heterocyclic quinonediimines
作者:O. Yu. Slabko、V. A. Kaminskii、M. N. Tilichenko
DOI:10.1007/bf00481519
日期:1989.11
Thio- and Selenocyanation Reactions of Quinone Imines—Derivatives of Pyrido[1,2-<i>a</i>]benzimidazole
作者:Oleg Y. Slabko、Andrey V. Kachanov、Vladimir A. Kaminskii
DOI:10.1080/00397911.2011.560743
日期:2012.8.15
The thio- and selenocyanation of quinone monoimines of pyrido[1,2-a]benzimidazole series with the participation of dithiocyanogen and triselenodicyanide in mild reaction conditions results in formation of 9- or 6-thiocyano- and 9-selenocyano-derivatives in good yields.
SLABKO, O. YU.;KAMINSKIJ, V. A.;TILICHENKO, M. N., XIMIYA GETEROTSIKL. SOED.,(1989) N1, S. 1500-1504
作者:SLABKO, O. YU.、KAMINSKIJ, V. A.、TILICHENKO, M. N.
DOI:——
日期:——
Synthesis of polynuclear heterocyclic quinone imines ? Derivatives of 4a,9-diazahydrofluoren-6-ones
作者:V. A. Kaminskii、O. Yu. Slabko、M. N. Tilichenko
DOI:10.1007/bf00475601
日期:1988.6
Selective monobromination in the series of quinoid pyrido[1,2-a]benzimidazole derivatives