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Cationic Rhodium(I)/BINAP-type bisphosphine complexes: Versatile new catalysts for highly chemo-, regio-, and enantioselective [2+2+2] cycloadditions

机译:阳离子铑(I)/ BINAP型双膦配合物:高度化学,区域和对映选择性[2 + 2 + 2]环加成反应的多功能新型催化剂

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摘要

Our research group was the first to discover that cationic rhodium(I)/BINAP-type bisphosphine complexes are versatile new catalysts for highly chemo-, regio-, and enantioselective [2+2+2] cycloadditions. The high chemo- and regioselectivity of these cycloadditions enabled efficient catalytic synthesis of substituted benzenes, cyclophanes, and nitrogen heterocycles. Furthermore, enantioselective variants of these cycloadditions were also developed that realized efficient catalytic constructions of axial, planar, central, and spiro chirality. 1 Introduction 2 Chemo- and Regioselective [2+2+2] Cycloadditions 2.1 [2+ 2-12] Cycloaddition of Terminal Alkynes 2.2 [2-11 2-12] Cycloaddition of Two Different Alkynes 2.3 [2-2+2] Cycloaddition of alpha,omega)-Diynes with Alkynes 2.4 [2 +2+21 Cycloaddition of Alkynes with Isocyanates, Isothiocyanates, and Carbon Disulfide 2.5 [2+2-12] Cycloaddition of Alkynes with Nitriles 3 Enantioselective [2+2+21 Cycloadditions 3.1 Construction of Axial Chirality 3.2 Construction of Planar Chirality 3.3 Construction of Central Chirality 3.4 Construction of Spiro Chirality 4 Summary
机译:我们的研究小组是第一个发现阳离子铑(I)/ BINAP型双膦配合物是用于高度化学,区域和对映选择性[2 + 2 + 2]环加成反应的多功能新型催化剂。这些环加成物的高化学选择性和区域选择性使得能够高效催化合成取代的苯,环烷和氮杂环。此外,还开发了这些环加成的对映选择性变体,实现了轴向,平面,中心和螺旋手性的高效催化结构。 1简介2化学和区域选择性[2 + 2 + 2]环加成2.1 [2+ 2-12]末端炔烃的环加成2.2 [2-11 2-12]两种不同炔烃的环加成2.3 [2-2 + 2]环加成α,ω)-二炔与炔烃的比较[2.4 + 2 + 21炔烃与异氰酸酯,异硫氰酸酯和二硫化碳的加成反应2.5 [2 + 2-12]炔烃与腈的加成反应3对映选择性[2 + 2 + 21环加成反应3.1轴向手性的构建3.2平面手性的构建3.3中心手性的构建3.4螺旋手性的构建4总结

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