Institut für Organische Chemie, Universität Regensburg, Universitätsstrasse 31, D-93053 Regensburg, Germany.
Org Lett. 2010 Oct 15;12(20):4552-5. doi: 10.1021/ol101854r.
An efficient, oxidative carbene-catalyzed lactonization reaction has been developed. Using thiazolium precatalysts, a variety of benzodioxepinone products are accessible in good to excellent yields under mild and operationally simple conditions. The reaction does not require high dilution conditions and proceeds via mild and selective oxidation with azobenzene, which can easily be recovered and reused applying inexpensive FeCl(3) as a formal terminal oxidant.
一种高效的、氧化卡宾催化的内酯化反应已经被开发出来。使用噻唑鎓前催化剂,在温和且操作简单的条件下,可以以良好到优异的产率得到各种苯并二氧杂环庚酮产物。该反应不需要高稀释条件,并且通过温和且选择性的氧化作用进行,使用偶氮苯作为氧化剂,反应结束后可以很容易地回收和重复使用,并且使用廉价的三氯化铁作为正式的终端氧化剂。