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Chem Commun (Camb). 2010 Feb 28;46(8):1347-9. doi: 10.1039/b917777a. Epub 2010 Jan 11.
The first chemoselective direct dehydrative cross-coupling of tautomerizable heterocycles with alkynes has been achieved via C-H/C-OH bond activations with direct C(sp(2))-C(sp) bond formation, which is in line with ideal synthesis using readily available materials.
通过 C-H/C-OH 键的活化以及直接的 C(sp(2))-C(sp) 键形成,实现了首例可互变异构的杂环与炔烃的化学选择性直接脱水交叉偶联反应,符合使用易得原料的理想合成。