首页> 外文期刊>Tetrahedron, Asymmetry: The International Journal for Repid Publication on all Aspects of Asymmetry in Orgainc, Inorganic, Organometallic, Physical and Bio-Organic Chemistry >The first example of a (1R,2S,5R)-(-)-menthyl chiral auxiliary in intramolecular nitrilimine cycloadditions: synthesis of enantiopure pyrazolo [1,5-a] [4,1]benzoxazepines and pyrazolo[1,5-a][4,1]benzodiazepines
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The first example of a (1R,2S,5R)-(-)-menthyl chiral auxiliary in intramolecular nitrilimine cycloadditions: synthesis of enantiopure pyrazolo [1,5-a] [4,1]benzoxazepines and pyrazolo[1,5-a][4,1]benzodiazepines

机译:分子内腈亚胺环加成反应中的(1R,2S,5R)-(-)-薄荷基手性助剂的第一个实例:对映体纯吡唑并[1,5-a] [4,1]苯并ze氮杂和吡唑并[1,5-a ] [4,1]苯并二氮杂s

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摘要

By using (1R,2S,5R)-(-)-menthyl as a chiral auxiliary, we have developed a synthesis of hydrazonoyl chlorides 2 and 8, treatment of which with silver carbonate promoted the in situ generation of the corresponding nitrilimines 3 and 9. The latter underwent intramolecular cycloaddition giving, respectively, enantiopure pyrazolo[1,5-a][4,1]benzoxazepines 4, 5 and pyrazolo[1,5-a][4,1]benzodiazepines 10.
机译:通过使用(1R,2S,5R)-(-)-薄荷基作为手性助剂,我们开发了酰氯2和8的合成,用碳酸银处理可促进原位生成相应的腈3和9。后者进行了分子内环加成,分别得到对映体纯的吡唑并[1,5-a] [4,1]苯并x氮平4,5和吡唑并[1,5-a] [4,1]苯并二氮杂10.10。

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