114560-12-2Relevant academic research and scientific papers
2-cyclopropylindoloquinones and their analogues as bioreductively activated antitumor agents: Structure-activity in vitro and efficacy in vivo
Naylor, Matthew A.,Jaffar, Mohammed,Nolan, John,Stephens, Miriam A.,Butler, Susan,Patel, Kantilal B.,Everett, Steven A.,Adams, Gerald E.,Stratford, Ian J.
, p. 2335 - 2346 (2007/10/03)
A series of 2-cycloalkyl- and 2-alkyl-3-(hydroxymethyl)-1- methylindoloquinones and corresponding carbamates have been synthesized and substituted in the 5-position with a variety of substituted and unsubstituted aziridines. Cytotoxicity against hypoxic c
Indoloquinone compounds
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, (2008/06/13)
Indoloquinone compounds useful as cytostatic agents have formula (I), where R2 and R3 are in each case, hydrogen, halogen, an alkyl group (which may be substituted), an alkoxy group or an aryloxy group, an alkylthio group or an arylt
STEREO- AND ENANTIOSELECTIVE SYNTHESES OF 2,3-DIHYDROINDOLE DERIVATIVES
Spackamp, W. Nico
, p. 211 - 234 (2007/10/02)
2,3-Dihydroindoles (2,3-Indolines) can be obtained in a highly stereoselective fashion through 1,5-electrocyclization of ortho-substituted aminobenzenes.The scope and mechanism of this novel process are discussed and also some applications.In presence of
