Key Laboratory for Advanced Materials and Institute of Fine Chemicals, School of Chemistry & Molecular Engineering, East China University of Science and Technology, Meilong Road 130, Shanghai 200237, China.
J Org Chem. 2021 May 7;86(9):6765-6779. doi: 10.1021/acs.joc.1c00493. Epub 2021 Apr 14.
The gram-scale synthesis of 5,6-, 6,7-, and 7,8-chromene/chromane-type aryne precursors and their applications in regioselective transformation to other functional derivatives is reported. Chromene/chromane-type arynes are generated under mild conditions, which can further undergo [2 + 2], [3 + 2], and [4 + 2] cycloaddition reactions, nucleophilic addition reactions, and σ-insertion reactions to produce structurally novel substituted chromenes and chromanes. The excellent regioselectivity of the reaction is facilitated by the oxygen-containing guiding groups at the -position of the triple bond, which can be removed or switched to other functional groups including alkenyl, aryl, heteroaryl, and arylamino groups.
本文报道了 5,6-、6,7-和 7,8-色烯/色满型芳炔前体的克级合成及其在区域选择性转化为其他功能衍生物中的应用。在温和条件下生成色烯/色满型芳炔,其可进一步进行[2+2]、[3+2]和[4+2]环加成反应、亲核加成反应和σ-插入反应,生成结构新颖的取代色烯和色满。由于三键的-位含有含氧导向基团,反应具有优异的区域选择性,该导向基团可以被去除或转换为其他官能团,包括烯基、芳基、杂芳基和芳氨基。