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Ligand-free MnBr2-Catalyzed Chemo- and Stereoselective Hydroboration of Terminal Alkynes
Chemistry - An Asian Journal ( IF 4.1 ) Pub Date : 2024-03-21 , DOI: 10.1002/asia.202400158
Rameshwar B. Pawar 1 , Mital H. Karmur 1 , Benudhar Punji 2
Affiliation  

A straightforward and ligand-free manganese-catalyzed protocol for the chemo- and stereoselective hydroborylation of alkynes with HBpin is demonstrated. This atom-economical reaction is highly selective for the synthesis of (E)-alkenylboronates, and tolerates important functionalities, including halides, ether, alkenyl, silyl and thiophenyl groups. A preliminary mechanistic study supports the involvement of a metal-hydride intermediate.

中文翻译:

无配体 MnBr2 催化末端炔烃的化学和立体选择性硼氢化

展示了一种简单且无配体的锰催化方案,用于使用 HBpin 对炔烃进行化学和立体选择性硼氢化反应。这种原子经济反应对于 ( E )-烯基硼酸酯的合成具有高度选择性,并且能够耐受重要的官能团,包括卤化物、醚、烯基、甲硅烷基和苯硫基。初步的机理研究支持金属氢化物中间体的参与。
更新日期:2024-03-21
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