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作 者:金小平[1] 张莉[2] 高浩其[3] 房江华[3] 李瑞丰[2] 方烨汶[3,4]
机构地区:[1]浙江医药高等专科学校基础部,宁波315100 [2]太原理工大学化学化工学院,太原030024 [3]宁波工程学院化学工程学院,宁波315016 [4]宁波现代精细化工有限公司,宁波315204
出 处:《化学进展》2013年第11期1898-1905,共8页Progress in Chemistry
基 金:国家自然科学基金项目(No.21202090);宁波市科技创新团队项目(No.2011B2002);浙江省自然科学基金项目(No.LY12B02001);宁波市自然科学基金项目(No.2011A610123;2012A610123)资助
摘 要:烷基芳基醚广泛存在于天然产物和药物分子中。钯和铜催化构筑C—O键的方法已成为合成烷基芳基醚的有效策略。本文总结了钯和铜催化的脂肪醇芳基化反应的最新研究进展。以Buchwald小组发展的基于联苯骨架的二叔丁基取代单膦配体,Hartwig小组发展的基于五苯基取代的二茂铁骨架的二叔丁基取代单膦配体或Beller小组发展的基于二吡唑骨架的二金刚烷基取代的单膦配体,可高效实现钯催化的各类脂肪醇和芳基卤代烃的C—O偶联。在铜催化反应条件下,1,10-菲罗啉及其衍生物和β-二羰基化合物是反应活性最高的两类配体。总的来说,和铜催化条件相比,钯催化的C—O偶联反应具有反应条件温和,官能团兼容性好,底物普适性广等优点。此外,对两类催化体系在配体选用、反应活性、β-H消除反应和反应机理等方面的差异进行了探讨。设计与合成新型配体被认为是C—O偶联反应取得进一步发展的关键。Alkyl aryl ethers are present in many naturally occurring and medicinally relevant compounds. Palladium- and copper-catalyzed C—O bond formation reactions have become effective strategies for their preparation. Recent developments in palladium- and copper-catalyzed arylations of aliphatic alcohols are summarized in this review. Palladium-catalyzed C—O cross coupling of various aliphatic alcohols with aryl halides could be efficiently realized in the presence of di-tert-buthyl biarylphosphine ligand, di-tert-buthylphosphino pentaphenylferrocene ligand, or di-adamantyl-substituted Bippyphos ligand developed by Buchwald, Hartwig, and Beller groups respectively. With the copper catalyst, 1, 10-phenanthroline and its derivatives, β-dicarbonyl compounds were served as the most efficient ligands. Generally, palladium-catalyzed C—O cross-coupling reactions display mild reaction conditions, good functional-group compatability, and broad substrate scope compared to the copper catalyst system. Moreover, the difference of the two catalytic systems including the choice of ligand, reactivity, β-H elimination and mechanism is discussed. The design and synthesis of new ligands are the key point for the further development of the C—O cross coupling.
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