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Radical Cyclization of Epoxy Vinyl- and Allylsulfones Promoted by Titanocene Chloride
The Journal of Organic Chemistry ( IF 3.3 ) Pub Date : 2015-04-15 00:00:00 , DOI: 10.1021/acs.joc.5b00206
A. Fernández-Mateos 1 , S. Encinas Madrazo 1 , P. Herrero Teijón 1 , R. Rubio González 1
Affiliation  

A titanocene-mediated intramolecular radical addition of different epoxy vinyl- and allylsulfones has been achieved. Five- and six-membered ring products were obtained in good to excellent yields in the presence of both 2.2 and 0.2 equiv of Cp2TiCl. A novel double-activation strategy allowed us to achieve small-size rings such as cyclobutanes and cyclopropanes.

中文翻译:

钛新世氯化物促进的环氧乙烯基和烯丙基砜的自由基环化

已经实现了钛茂介导的不同环氧乙烯基和烯丙基砜的分子内自由基加成。在2.2和0.2当量的Cp 2 TiCl的存在下,以良好至优异的产率获得了五元和六元环产物。一种新颖的双重激活策略使我们能够获得小尺寸的环,例如环丁烷和环丙烷。
更新日期:2015-04-15
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