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通过钯催化的分子内氧化偶联以及随后带有胺的杂芳基磺酰胺的亲核环开环反应获得联芳基磺酰胺。

Access to biaryl sulfonamides by palladium-catalyzed intramolecular oxidative coupling and subsequent nucleophilic ring opening of heterobiaryl sultams with amines.

机构信息

Department of Pharmaceutical Technology (Process Chemistry), National Institute of Pharmaceutical Education and Research , S. A. S. Nagar, Punjab 160062, India.

出版信息

Org Lett. 2015 Mar 6;17(5):1296-9. doi: 10.1021/acs.orglett.5b00290. Epub 2015 Feb 24.

Abstract

The installation of sulfonamide pharmacophores on heterobiaryls has successfully been executed by a previously unknown palladium-catalyzed intramolecular oxidative coupling in N-arylsulfonyl heterocycles followed by novel ring opening of heterobiaryl sultams with amine nucleophiles. The protocol has a wide scope of substrates warranting broad applications in the synthesis of heterobiaryls containing an o-sulfonyl or carboxyl functional group.

摘要

通过一种先前未知的钯催化的 N-芳基磺酰基杂环分子内氧化偶联,随后用胺亲核试剂打开杂双芳基磺酰胺的新型环,成功地在杂双芳基上安装磺胺类药效团。该方案具有广泛的底物范围,保证了在含有邻磺酰基或羧基官能团的杂双芳基合成中的广泛应用。

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