首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Synthesis of novel chiral bis(2-oxazolinyl)xanthene (xabox) ligands and their evaluation in catalytic asymmetric 1,3-dipolar cycloaddition reactions of nitrones with 3-crotonoyl-2-oxazolidinone
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Synthesis of novel chiral bis(2-oxazolinyl)xanthene (xabox) ligands and their evaluation in catalytic asymmetric 1,3-dipolar cycloaddition reactions of nitrones with 3-crotonoyl-2-oxazolidinone

机译:新型手性双(2-恶唑啉基)氧杂蒽(xabox)配体的合成及其在硝酮与3-巴豆酰-2-恶唑烷酮的催化不对称1,3-偶极环加成反应中的评价

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摘要

Chiral 4,5-bis(2-oxazolinyl)-(2,7-di-tert-butyl-9,9-dimethyl)-9H-xanthenes (xabox) were synthesized and the chiral environments were evaluated in catalytic asymmetric 1,3-dipolar cycloaddition reactions of nitrones resulting in good to excellent enantioselectivities. 1,3-Dipolar cycloaddition reactions of nitrones with 3-crotonoyl-2-oxazolidinone in the presence of a bis(2-oxazolinyl)xanthene (4c; xabox-Bn) and Mn(II) or Mg(II) complex as a chiral Lewis acid catalyst proceeded smoothly to give the corresponding cycloadducts ranging from 96:4 to >99:1 of endo:exo ratio and ranging from 91% to 98% ee for the endo adduct.
机译:合成了手性4,5-双(2-恶唑啉基)-(2,7-二叔丁基-9,9-二甲基)-9H-氧杂蒽(xabox),并在催化不对称1,3中评估了手性环境硝基的-偶极环加成反应导致良好至优异的对映选择性。在双(2-恶唑啉基)x吨(4c; xabox-Bn)和Mn(II)或Mg(II)配合物的存在下,硝酮与3-巴豆酰基-2-恶唑烷酮的1,3-偶极环加成反应路易斯酸催化剂平稳地进行,得到相应的环加合物,其内消旋比为96:4至> 99:1,内消旋加合物的ee为91%至98%。

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