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三氮烯与一氧化二氮的合成。

Synthesis of triazenes with nitrous oxide.

机构信息

Institut des Sciences et Ingénierie Chimiques, Ecole Polytechnique Fédérale de Lausanne (EPFL), 1015 Lausanne (Switzerland).

出版信息

Angew Chem Int Ed Engl. 2015 Jan 2;54(1):302-5. doi: 10.1002/anie.201408597. Epub 2014 Oct 21.

Abstract

Triazenes are valuable compounds in organic chemistry and numerous applications have been reported. Furthermore, triazenes have been investigated extensively as potential antitumor drugs. Here, we describe a new method for the synthesis of triazenes. The procedure involves a reagent which is rarely used in synthetic organic chemistry: nitrous oxide (N2 O, "laughing gas"). Nitrous oxide mediates the coupling of lithium amides and organomagnesium compounds while serving as a nitrogen donor. Despite the very inert character of nitrous oxide, the reactions can be performed in solution under mild conditions. A key advantage of the new procedure is the ability to access triazenes with alkynyl and alkenyl substituents. These compounds are difficult to prepare by conventional methods because the required starting materials are unstable. Some of the new alkynyltriazenes were found to display high cytotoxicity in in vitro tests on ovarian and breast cancer cell lines.

摘要

三氮烯是有机化学中很有价值的化合物,已有大量应用报道。此外,三氮烯还被广泛研究作为潜在的抗肿瘤药物。在这里,我们描述了一种新的三氮烯合成方法。该方法涉及一种在合成有机化学中很少使用的试剂:一氧化二氮(N2O,“笑气”)。一氧化二氮作为氮供体介导了酰胺和有机镁化合物的偶联。尽管一氧化二氮的惰性很强,但反应可以在温和的条件下在溶液中进行。该新方法的一个关键优势是能够获得带有炔基和烯基取代基的三氮烯。这些化合物很难通过常规方法制备,因为所需的起始材料不稳定。一些新的炔基三氮烯在卵巢癌和乳腺癌细胞系的体外试验中显示出很高的细胞毒性。

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