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钯催化 1,8-二碘萘与叔炔丙醇的双环化反应生成菲啰啉酮及其作为氟离子荧光化学传感器的应用。

Palladium catalyzed bicyclization of 1,8-diiodonaphthalene and tertiary propargylic alcohols to phenalenones and their applications as fluorescent chemosensor for fluoride ions.

机构信息

Department of Chemistry, Zhejiang University, Hangzhou, P R China.

出版信息

Chem Commun (Camb). 2011 Mar 7;47(9):2628-30. doi: 10.1039/c0cc04875e. Epub 2011 Jan 13.

DOI:10.1039/c0cc04875e
PMID:21234483
Abstract

Phenalenone derivatives were efficiently constructed from 1,8-diiodonaphthalene and tertiary propynols via a one-pot domino reaction which eventually included Pd-catalyzed Sonogoshira coupling, Pd-catalyzed allylic oxidation and Pd-catalyzed C(sp(2))-H activation. Moreover, the synthesized phenalenone derivative presented a practical application as a fluorescent chemosensor for fluoride anion with high sensitivity and selectivity.

摘要

菲咯啉酮衍生物可由 1,8-二碘萘和三级丙炔醇通过一锅多米诺反应高效构建,该反应最终包括 Pd 催化的 Sonogoshira 偶联、Pd 催化的烯丙基氧化和 Pd 催化的 C(sp(2))-H 活化。此外,合成的菲咯啉酮衍生物可用作对氟离子具有高灵敏度和选择性的荧光化学传感器。

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