Synthesis of Seleno-Dibenzocycloheptenones/Spiro[5.5]Trienones by Radical Cyclization of Biaryl Ynones

被引:28
|
作者
Goulart, Helen A. [1 ]
Bartz, Ricardo H. [1 ]
Peglow, Thiago J. [1 ]
Barcellos, Angelita M. [1 ]
Cervo, Rodrigo [2 ]
Cargnelutti, Roberta [2 ]
Jacob, Raquel G. [1 ]
Lenardao, Eder J. [1 ]
Perin, Gelson [1 ]
机构
[1] Univ Fed Pelotas UFPel, Lab Sintese Organ Limpa LASOL, CCQFA, BR-35496010 Pelotas, RS, Brazil
[2] Univ Fed Santa Maria UFSM, Dept Quim, CCNE, BR-97105900 Santa Maria, RS, Brazil
来源
JOURNAL OF ORGANIC CHEMISTRY | 2022年 / 87卷 / 06期
关键词
INTRAMOLECULAR NICHOLAS REACTIONS; ANTITUMOR AGENTS; ORGANOSELENIUM CHEMISTRY; ANTITUBULIN ACTIVITY; SELENIUM; COLCHICINE; SESQUITERPENE; EFFICIENT; ANALOGS; ACCESS;
D O I
10.1021/acs.joc.1c03112
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
We report herein an alternative method for the synthesis of seleno-dibenzocycloheptenones and seleno-spiro[5.5]-trienones through the radical cyclization of biaryl ynones in the presence of diorganyl diselenides, using Oxone as a green oxidizing agent. The reactions were conducted using acetonitrile as the solvent in a sealed tube at 100 degrees C. The protocol is operationally simple and scalable, exhibits high regioselectivity, and allows the synthesis of 24 dibenzocycloheptenones/spiro[5.5]trienones in yields of up to 99%, 17 of which are unpublished compounds. Additionally, synthetic transformations of the prepared compounds, such as oxidation and reduction reactions, are demonstrated.
引用
收藏
页码:4273 / 4283
页数:11
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