Division of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore.
Org Lett. 2010 May 7;12(9):2052-5. doi: 10.1021/ol100522z.
A copper-catalyzed reaction of alpha-azidocarbonyl compounds under an oxygen atmosphere is reported where nitriles are formed via C-C bond cleavage of a transient iminyl copper intermediate. The transformation is carried out by a sequence of denitrogenative formation of iminyl copper species from alpha-azidocarbonyl compounds and their C-C bond cleavage, where molecular oxygen (1 atm) is a prerequisite to achieve the catalytic process and one of the oxygen atoms of O(2) was found to be incorporated into the beta-carbon fragment as a carboxylic acid.
报道了一种在氧气氛围下,通过α-叠氮羰基化合物的铜催化反应,经由瞬态亚氨基铜中间体的 C-C 键断裂生成腈的反应。该转化通过从α-叠氮羰基化合物中形成亚氨基铜物种的脱氮反应和它们的 C-C 键断裂来进行,其中分子氧(1 大气压)是实现催化过程的前提条件,并且发现 O(2)中的一个氧原子被掺入到β-碳片段中作为羧酸。