化学
磷化氢
硼烷
立体选择性
硼烷
药物化学
硼
有机化学
催化作用
作者
Sylwia Sowa,K. Michał Pietrusiewicz
出处
期刊:Tetrahedron
[Elsevier BV]
日期:2021-03-05
卷期号:86: 132057-132057
被引量:3
标识
DOI:10.1016/j.tet.2021.132057
摘要
Abstract A new method for reduction of tertiary phosphine oxides leading to the formation of tertiary phosphine-boranes has been developed. The BH3-THF/Ti(Oi-Pr)4 reducing system enables conversion of triaryl, diarylalkyl and trialkylphosphine oxides directly to their borane analogues in good to high yields. In contrast to the previously reported protocols, the presence of activating groups in the structure of starting material is not necessary for the reaction to occur. The reaction is highly stereoselective and proceeds with predominant retention of configuration at the phosphorus atom. A plausible mechanism of reduction of the P O bond by BH3-THF/Ti(Oi-Pr)4 has been proposed.
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