Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University (TMDU), 2-3-10 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-0062, Japan.
Org Biomol Chem. 2020 Feb 26;18(8):1550-1562. doi: 10.1039/c9ob02698c.
The recent remarkable progress in azide chemistry has realized sequential conjugation methods with selective 1,2,3-triazole formation. On the basis of the diverse reactivities of azides and azidophiles, including terminal alkynes and cyclooctynes, various selective reactions to furnish triazoles and a wide range of platform molecules, such as diynes, diazides, triynes, and triazides, have been developed so far for bis- and tris(triazole) syntheses. This review highlights recent transformations involving selective triazole formation, allowing the efficient preparation of unsymmetric bis- and tris(triazole)s using diverse platform molecules.
近年来,叠氮化学取得了显著进展,实现了具有选择性 1,2,3-三唑形成的顺序共轭方法。基于叠氮化物和叠氮化物亲电试剂的不同反应性,包括末端炔烃和环辛炔,迄今为止已经开发了各种选择性反应来提供三唑和广泛的平台分子,如二炔、二叠氮化物、三炔和三叠氮化物,用于双和三(三唑)合成。这篇综述强调了涉及选择性三唑形成的最新转化,允许使用各种平台分子高效制备不对称双和三(三唑)。