首页> 外文期刊>European journal of organic chemistry >Effects of Extended Aryl-Substituted Bisoxazoline Ligands in Asymmetric Synthesis - Efficient Synthesis and Application of 4,4'-Bis(l-Naphthyl)-,4,4'-Bis(2-Naphthyl)-and 4,4'-Bis(9-Anthryl)-2,2'-isopropylidenebis(l,3-oxazolines)
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Effects of Extended Aryl-Substituted Bisoxazoline Ligands in Asymmetric Synthesis - Efficient Synthesis and Application of 4,4'-Bis(l-Naphthyl)-,4,4'-Bis(2-Naphthyl)-and 4,4'-Bis(9-Anthryl)-2,2'-isopropylidenebis(l,3-oxazolines)

机译:芳基取代的双二恶唑啉配体在不对称合成中的作用-4,4'-双(1-萘基)-,4,4'-双(2-萘基)-和4,4'-双(高效合成和应用) 9-蒽基)-2,2'-异丙叉二(1,3-恶唑啉)

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摘要

The steric influence of extended aryl substituents on 2,2'-bis(l,3-oxazoline) ligands was investigated in a series of asymmetric catalytic reactions such as Mukaiyama aldol and Michael reactions,hetero-Diels-Alder processes,and allylic alkylation reactions.4,4'-(2-Naphthyl)- and 4,4'-(9-anthryl)-substituted isopropylidene-bridged 2,2'-bis(l,3-oxazolines) were synthesized and their enantioselective and catalytic properties in combination with different metals evaluated.
机译:通过一系列不对称催化反应,例如Mukaiyama aldol和Michael反应,杂Diels-Alder反应和烯丙基烷基化反应,研究了扩展的芳基取代基对2,2'-双(1,3-恶唑啉)配体的空间影响合成了.4,4'-(2-萘基)-和4,4'-(9-蒽基)取代的异亚丙基桥连的2,2'-双(1,3-恶唑啉),它们的对映选择性和催化性能在与不同金属的组合进行评估。

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