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1.
RSC Adv ; 11(51): 32295-32299, 2021 Sep 27.
Artigo em Inglês | MEDLINE | ID: mdl-35495535

RESUMO

Reactive oxygen and nitrogen species (ROS, RNS) are ubiquitous in biology with a variety of physiological and pathological functions. Here we describe a broad spectrum ROS/RNS detecting fluorogenic probe with red fluorescence emission and up to 100-fold gain. Hence these modified probes are useful for in vivo non-invasive quantification of ROS/RNS.

2.
Org Lett ; 22(23): 9196-9198, 2020 12 04.
Artigo em Inglês | MEDLINE | ID: mdl-33196197

RESUMO

In stark contrast to phenothiazines and their prevalence for cross-dehydrogenative amination reactions, benzophenothiazine has a pronounced preference for cross-dehydrogenative C-C bond-forming reactions. Moreover, the substrate is very versatile, leading to several new classes of C-C bond-forming reactions and many new oxidative coupling product architectures, including unprecedented indole fused paddlewheel-like structures.

3.
Chem Commun (Camb) ; 56(86): 13185-13188, 2020 Nov 07.
Artigo em Inglês | MEDLINE | ID: mdl-33020764

RESUMO

Step and redox efficiencies are a rising priority in synthetic method development, in order to make synthetic processes more sustainable and more affordable. Herein, a step and redox efficient nitroarene to indole synthesis is developed, in sharp contrast to the rich literature on the construction of indoles. Elemental zinc was found to be the best terminal reductant.

4.
Org Lett ; 20(10): 2884-2887, 2018 05 18.
Artigo em Inglês | MEDLINE | ID: mdl-29701985

RESUMO

Phenothiazinimides, a fairly unknown class of imines, were prepared and found to be very reactive as ultrasimple atom-efficient electrophilic amination reagents for phenols and indoles under metal-free conditions.

5.
Chemistry ; 22(50): 17980-17982, 2016 Dec 12.
Artigo em Inglês | MEDLINE | ID: mdl-27731915

RESUMO

The Ru catalyzed cross-dehydrogenative C-O bond formation between anilines and phenols is described and discussed. The exclusive C-O versus C-N bond-formation selectivity, moreover in the absence of chelating-assisting directing groups and while leaving the N-H position untouched, is a remarkable feature of this metal-catalyzed radical cross-dehydrogenative coupling.

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