Hydroboration of alkynes initiated by sodium triethylborohydride

被引:4
|
作者
Maj, Anna M. [1 ,2 ]
Szarlan, Bartlomiej [2 ,3 ]
Pawluc, Piotr [2 ,3 ]
Zaranek, Maciej [2 ,3 ]
机构
[1] Univ Technol & Life Sci Bydgoszcz, Fac Chem Technol & Engn, Seminaryjna St 3, PL-85326 Bydgoszcz, Poland
[2] Adam Mickiewicz Univ, Ctr Adv Technol, Uniwersytetu Poznanskiego St 10, PL-61614 Poznan, Poland
[3] Adam Mickiewicz Univ, Fac Chem, Uniwersytetu Poznanskiego St 8, PL-61614 Poznan, Poland
关键词
Hydroboration; Alkynes; Transition-metal-free; Borohydrides; CATALYTIC HYDROBORATION; ALKENES; HYDROSILYLATION; BORYLATION;
D O I
10.1016/j.poly.2022.115961
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Sodium triethylborohydride, a popular hydride transferring reagent, is commonly used as an activating agent for hydroboration catalysts based on the first-row transition metal complexes. It has been found that NaHBEt3 can be a selective catalyst for hydroboration of terminal alkynes with pinacolborane. Hydroboration of aromatic and aliphatic alkynes in the presence of 10 mol% of NaHBEt3 proceeded in a highly selective manner to give (E)-vinylboronate esters with high yields, whereas ethynylsilanes seem to be less reactive in this process. Internal alkynes can also be transformed into corresponding vinylboronate esters, however, this process require prolonged reaction times compared to their terminal counterparts.
引用
收藏
页数:5
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