首页> 外文期刊>The Journal of Organic Chemistry >Design, synthesis, and applications of potential substitutes of t-Bu-phosphinooxazoline in Pd-catalyzed asymmetric transformations and their use for the improvement of the enantioselectivity in the Pd-catalyzed allylation reaction of fluorinated allyl enol carbonates
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Design, synthesis, and applications of potential substitutes of t-Bu-phosphinooxazoline in Pd-catalyzed asymmetric transformations and their use for the improvement of the enantioselectivity in the Pd-catalyzed allylation reaction of fluorinated allyl enol carbonates

机译:t-Bu-膦基恶唑啉在Pd催化的不对称转化中的潜在替代物的设计,合成及其应用,及其在改进Pd催化的氟代烯丙基碳酸烯丙酯的Pd烯丙基化反应中对映选择性的应用

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摘要

The design, synthesis, and applications of potential substitutes of t-Bu-PHOX in asymmetric catalysis is reported. The design relies on the incorporation of geminal substituents at C5 in combination with a substituent at C4 other than t-butyl (i-Pr, i-Bu, or s-Bu). Most of these new members of the PHOX ligand family behave similarly in terms of stereoinduction to t-Bu-PHOX in three palladium-catalyzed asymmetric transformations. Electronically modified ligands were also prepared and used to improve the enantioselectivity in the Pd-catalyzed allylation reaction of fluorinated allyl enol carbonates.
机译:报道了在不对称催化中t-Bu-PHOX的潜在替代品的设计,合成和应用。该设计依赖于在C5处引入双取代基与在C4处除了叔丁基(i-Pr,i-Bu或s-Bu)以外的取代基结合。在3种钯催化的不对称转化中,PHOX配体家族的大多数新成员在立体诱导方面与t-Bu-PHOX相似。还制备了电子修饰的配体,并用于改善氟化烯丙基烯醇碳酸酯在Pd催化的烯丙基化反应中的对映选择性。

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