2-substituted H-1-perimidines are readily prepared, in high yields, by refluxing a mixture of sodium pyrosulfite, an aldehyde, and 1,8-diaminonaphthalene in aqueous ethanol or N,N-dimethylformamide. The method is of wide applicability except from araldehydes bearing a strong electron-withdrawing group (-CN, -NO2).
STARSHIKOV N. M.; POZHARSKIJ A., XIMIYA GETEROTSIKL. SOEDIN., 1980, HO 1, 96-100
作者:STARSHIKOV N. M.、 POZHARSKIJ A.
DOI:——
日期:——
STARSHCHIKOV N. M.; POZHARSKIJ A. F.; POZHARSKIJ F. T., XIMIYA GETEROTSIKL. SOEDIN, 1977, HO 7, 986-988
作者:STARSHCHIKOV N. M.、 POZHARSKIJ A. F.、 POZHARSKIJ F. T.
DOI:——
日期:——
[EN] INHIBITORS OF ANDROGEN RECEPTOR ACTIVATION FUNCTION-2 (AF2) AS THERAPEUTICS AND METHODS FOR THEIR USE<br/>[FR] INHIBITEURS DE FONCTION D'ACTIVATION DE RÉCEPTEUR D'ANDROGÈNE 2 (AF2) EN TANT QU'AGENTS THÉRAPEUTIQUES ET PROCÉDÉS POUR LEUR UTILISATION
申请人:UNIV BRITISH COLUMBIA
公开号:WO2013023300A1
公开(公告)日:2013-02-21
This invention provides compound having a structure of Formula ((IA)/(IB)) or Formula ((IIA)/(IIB)) or Formula (III): Formula (IA) or Formula (IB) or Formula (IIA) (IIB) or (III). Uses of such compounds for treatment of various indications, including prostate cancer as well as methods of treatment involving such compounds are also provided.