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2H-氮杂环丁烷由烷基卡宾与腈基的协同加成得到。

2H-Azirines from a concerted addition of alkylcarbenes to nitrile groups.

机构信息

Physical Organic and Structural Chemistry, Institute of Organic Chemistry, University of Vienna, Wahringer Strasse 38, A-1090 Vienna, Austria.

出版信息

Org Lett. 2010 May 21;12(10):2366-9. doi: 10.1021/ol100703r.

Abstract

Photolysis of aziadamantanes in the presence of fumaronitrile (FN) unexpectedly afforded conjugated 2H-azirines resulting from addition of the carbene to the CN triple bond. This represents the first example of a direct azirine formation starting from an alkylcarbene for which a concerted pathway is postulated. The novel outcome of the reaction is favored by the prior formation of a carbene-alkene complex, a type of adduct that only recently has been described.

摘要

在富马腈 (FN) 的存在下,阿扎达曼烷的光解出人意料地生成了共轭的 2H-氮丙啶,这是由于卡宾加成到 CN 三键上。这代表了从烷基卡宾出发直接形成氮丙啶的首例例子,该反应被假定为协同途径。该反应的新颖结果是由先前形成的卡宾-烯烃配合物所促进的,这种加合物类型最近才被描述。

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