College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou 310014, P. R. China.
Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, Zhejiang University of Technology, Hangzhou 310014, P. R. China.
Org Lett. 2020 Mar 6;22(5):1709-1713. doi: 10.1021/acs.orglett.9b04555. Epub 2020 Feb 19.
Here, we report a chiral copper(II)-bisoxazoline-catalyzed enantioselective ring opening of cyclic diaryliodonium salts with heteroaryl thiols. The readily available 2-mercaptobenzoxazole and 2-mercaptobenzothiazole derivatives reacted efficiently with cyclic diaryliodonium salts and afforded various axially chiral biaryls bearing iodine and sulfur functional groups in excellent yields and enantioselectivities. The products were further transformed into diverse enantiopure alkyl biaryl sulfides, which can be employed as chiral ligands.
在这里,我们报告了一种手性铜(II)-双恶唑啉催化的环状二芳基碘鎓盐与杂芳基硫醇的对映选择性开环反应。易得的 2-巯基苯并恶唑和 2-巯基苯并噻唑衍生物与环状二芳基碘鎓盐反应高效,以优异的收率和对映选择性得到了各种含有碘和硫官能团的轴手性联芳基产物。产物进一步转化为多种手性纯烷基联芳基硫化物,可作为手性配体使用。