首页> 外文会议>IUPAC 10th International conference on novel materials and their synthesis: Book of abstracts >BIS-OXAZOLINES AS EFFECTIVE LIGANDS FOR PALLADIUM-CATALYZED COUPLING AND CARBONYLATION REACTIONS
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BIS-OXAZOLINES AS EFFECTIVE LIGANDS FOR PALLADIUM-CATALYZED COUPLING AND CARBONYLATION REACTIONS

机译:BIS-恶唑酮作为有效的配位体,用于钯催化的偶联和羰基化反应

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摘要

The synthesis and characterization of new bis (oxazoline) (BOX) ligands and their corresponding palladium complexes (Pd-BOX) was achieved. The catalytic activities of these new complexes were tested in Suzuki-Miyaura, Heck, and Sonogashira coupling reactions and in carbonylation reactions. Palladium-BOX complexes showed very high catalytic activities towards the coupling reactions with different aryl halides, aryl boronic acids, alkenes and alkynes and for the regioselective alkoxycarbonylation of alkynes. Various biaryls, substituted alkenes and alkynes, and unsaturated esters were produced in high yields and regioselectivity. The authors would like to acknowledge the support provided by King Abdulaziz City for Science and Technology (KACST) through the Science & Technology Unit at King Fahd University of Petroleum & Minerals (KFUPM) for funding this work through project No. 11-PET1665-04 as part of the National Science, Technology and Innovation Plan.
机译:实现了新的双(恶唑啉)(BOX)配体及其相应的钯配合物(Pd-BOX)的合成和表征。这些新的配合物的催化活性已在Suzuki-Miyaura,Heck和Sonogashira偶联反应以及羰基化反应中进行了测试。钯-BOX配合物对与不同的芳基卤化物,芳基硼酸,烯烃和炔烃的偶联反应和炔烃的区域选择性烷氧羰基化反应显示出很高的催化活性。以高收率和区域选择性制备了各种联芳基,取代的烯烃和炔烃以及不饱和酯。作者要感谢阿卜杜勒阿齐兹国王科技城(KACST)通过法赫德国王石油与矿产大学(KFUPM)的科学技术部门提供的支持,以通过项目11-PET1665-04资助这项工作。作为国家科技创新计划的一部分。

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