首页> 外文期刊>The Journal of Organic Chemistry >Radical hydrostannylation, pd(0)-catalyzed hydrostannylation, stannylcupration of propargyl alcohols and enynols: region- and steresoselectivities
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Radical hydrostannylation, pd(0)-catalyzed hydrostannylation, stannylcupration of propargyl alcohols and enynols: region- and steresoselectivities

机译:自由基加氢甲酸酯化,pd(0)催化的加氢甲酸酯化,炔丙醇和烯醇的苯乙烯醇化:区域和立体选择性

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摘要

Different enynols and propargyl derivativs were submitted to radical hydrostannylation (Bu_3SnH/ AIBN), Pd(0)-catalyzed hydrostannylation [Bu_3SnH/Pd(0), and stannylcupration [Bu_3Sn(R)CuNMLi_2] Conditions. Except for the radical stannylation reaction, high region- and stereoselective formation Of vinyl- and dienylstannanes are obtained. Results are tentatively explained in terms of steric Interactions between the alkyne or enyne substituents and the palladium or cuprate moieties in The different reaction intermediates.
机译:将不同的烯醇和炔丙基衍生基团用于自由基氢化锡烷基化(Bu_3SnH / AIBN),Pd(0)催化的氢化锡烷基化[Bu_3SnH / Pd(0)和甲锡化[Bu_3Sn(R)CuNMLi_2]条件。除了自由基的甲锡烷基化反应以外,还可以获得乙烯基和二烯基锡烷的高区域选择性和立体选择性形成。用不同反应中间体中炔或烯炔取代基与钯或铜酸根部分之间的空间相互作用来初步解释结果。

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