区域选择性
电泳剂
烷基
化学
卡宾
催化作用
卤化物
终端(电信)
组合化学
炔烃
铜
药物化学
有机化学
计算机科学
电信
作者
Yang Gao,Nana Kim,S Yazdani,Mingyu Liu,Aaron Kendrick,Douglas B. Grotjahn,Guy Bertrand,Rodolphe Jazzar,Keary M. Engle
出处
期刊:Le Centre pour la Communication Scientifique Directe - HAL - memSIC
日期:2022-02-01
标识
DOI:10.26434/chemrxiv-2022-z4wg2
摘要
Cyclic(alkyl)(amino)carbene (CAAC) ligands are found to perturb regioselectivity of the copper-catalyzed carboboration of terminal alkynes, favoring the less commonly observed internal alkenylboron regiosomer through an α-selective borylcupration step. A variety of carbon electrophiles participate in the reaction, including allyl alcohols derivatives and alkyl halides. The method provides a straightforward and selective route to versatile tri-substituted alkenylboron compounds that are otherwise challenging to access.
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