Department of Chemistry, University of Virginia , Charlottesville, Virginia 22904-4319, United States.
Org Lett. 2017 Sep 15;19(18):4790-4793. doi: 10.1021/acs.orglett.7b02178. Epub 2017 Aug 25.
Dioxiranes are among the most selective and useful reagents for C(sp)-H hydroxylation, but the development of a general dioxirane-mediated catalytic method has been an elusive goal. A trifluoromethyl ketone catalyst in combination with Oxone is shown to enable the first dioxirane-mediated catalytic hydroxylations that approximate the reactivity and selectivity of isolated dioxiranes. The mild reaction conditions allow for selective 3° hydroxylation and 2° oxidation and are tolerant of acid-sensitive functionality and electron-neutral arenes.
环氧化合物是 C(sp3)-H 羟基化反应中最具选择性和最有用的试剂之一,但开发一种通用的环氧化合物介导的催化方法一直是一个难以实现的目标。三氟甲基酮催化剂与 Oxone 的结合证明可以实现第一个接近分离环氧化合物的反应活性和选择性的环氧化合物介导的催化羟基化反应。温和的反应条件允许选择性的 3°羟基化和 2°氧化,并且对酸敏感的官能团和电中性芳环具有耐受性。