C-H functionalization of (hetero)arenes: Direct selanylation mediated by Selectfluor

被引：22

作者：

Belladona, Andrei L. ^{[1
]}

Cervo, Rodrigo ^{[1
]}

Alves, Diego ^{[2
]}

Barcellos, Thiago ^{[3
]}

Cargnelutti, Roberta ^{[1
]}

Schumacher, Ricardo F. ^{[1
]}

机构：

[1] Fed Univ Santa Maria UFSM, Dept Chem, BR-97105900 Santa Maria, RS, Brazil

[2] Fed Univ Pelotas UFPel, CCQFA, LASOL, POB 354, BR-96010310 Pelotas, RS, Brazil

[3] Univ Caxias UCS, Lab Biotechnol Nat & Synthet Prod, Caxias Do Sul, RS, Brazil

来源：

TETRAHEDRON LETTERS | 2020年 / 61卷 / 26期

关键词：

Selectfluor; N-Heterocycles; Diaryl diselenide; Selanylation reaction; C-H functionalization; ASSISTED SYNTHESIS; DERIVATIVES; ANTIOXIDANT; EFFICIENT; INDOLES; THIOLATION; SELENATION; SELENIDES; ARENES; CUI;

D O I：

10.1016/j.tetlet.2020.152035

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The direct selanylation of a diverse array of (hetero)arenes, including imidazo[2, 1-b]thiazole, imidazo [1, 2-a]pyridine, 1H-indole, 1H-pyrazole, isoxazole and naphthalen-2-ol is presented. The reactions are mediated by Selectfluor, as a stable, easy to handle and commercially available oxidant. The methodology features simple, mild and safe reaction conditions to produce non-symmetrical diorganyl selenides in moderate to excellent yields. The reactions were conducted at room temperature in air using NaHCO3 in acetonitrile. (C) 2020 Elsevier Ltd. All rights reserved.

引用

页数：4

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