A direct annulation reaction of N‐(2‐formylaryl)indoles has been developed, which can provide a new entry to biologically and medicinally important indole‐indolone scaffolds via a silver‐catalyzed direct oxidative coupling between aldehydeCH and sp2CH bonds for the first time. Remarkably, this strategy displayed excellent functional group compatibilities, thereby suggesting its wide potential for
Palladium-catalyzed cyclocarbonylation of cyclic diaryliodoniums: Synthesis of fluorenones
作者:Li Liu、Jian Qiang、Shuhua Bai、Yang Li、Chunbao Miao、Jian Li
DOI:10.1002/aoc.3817
日期:2017.12
An efficient approach to the synthesis of fluorenones via the palladium‐catalyzed cyclocarbonylation of cyclic diaryliodoniums was developed. Our route enables facile access to fluorenones with various substituents in modest to high yields.
[EN] NOVEL INDICATOR PLATFORM<br/>[FR] NOUVELLE PLATEFORME INDICATRICE
申请人:BIOSYNTH AG
公开号:WO2010128120A1
公开(公告)日:2010-11-11
A novel indicator platform comprises a plurality of 1 H-lndol-3-yl indicator compounds that are capable of converting to a signalophore compound in response to an external stimulus. In one class of indicator compounds, the resulting signalophores are 2-benzylideneindoline compounds that are formed by an intermolecular Aldol-type process; in a further class of indicator compounds, the resulting signalophores are 10H-indolo[1,2-a]indole compounds that are formed by an intramolecular Aldol-type process. The indicators can be used in a wide array of applications relating, for example, to biological systems or optical data storage.
Synthesis of 10<i>H</i>-indolo[1,2-<i>a</i>]indol-10-ones <i>via</i> palladium-catalyzed C–H bond activation and difluorocarbene transfer
作者:Chengxian Hu、Dan Mou、Xi Zhang、Ying Fu、Congde Huo、Zhengyin Du
DOI:10.1039/d2ob01493a
日期:——
A Pd-catalyzed annulation between 1-(2-iodophenyl)-1H-indoles and sodium difluorochloroacetate has been developed to synthesize 10H-indolo[1,2-a]indol-10-one derivatives via C–Hbondactivation and difluorocarbene transfer. Our route enables facile access to the targeted products with various substituents in moderate to high yields. This method features high reactivity, good functional group tolerance
A novel indicator platform comprises a plurality of 1H-Indol-3-yl indicator compounds that are capable of converting to a signalophore compound in response to an external stimulus. In one class of indicator compounds, the resulting signalophores are 2-benzylideneindoline compounds that are formed by an intermolecular Aldol-type process; in a further class of indicator compounds, the resulting signalophores are 10H-indolo[1,2-a]indole compounds that are formed by an intramolecular Aldol-type process. The indicators can be used in a wide array of applications relating, for example, to biological systems or optical data storage.