首页> 外文期刊>The Journal of Organic Chemistry >Ligand-Controlled Stereodivergent, Enantioselective Conjugate Addition of 2-Oxazoline- and 2-Thiazoline-4-carboxylate to Nitroalkene Catalyzed by Chiral Copper Complexes
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Ligand-Controlled Stereodivergent, Enantioselective Conjugate Addition of 2-Oxazoline- and 2-Thiazoline-4-carboxylate to Nitroalkene Catalyzed by Chiral Copper Complexes

机译:手性铜配合物催化2-恶唑啉-和2-噻唑啉-4-羧酸的配体控制的立体发散,对映选择性共轭加成反应

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摘要

The copper-catalyzed asymmetric conjugate addition of 2-oxazoline- and 2-thiazoline-4-carboxylate to a nitroalkene proceeded to give either the syn or anti adduct selectively in high enantiomeric excess when an appropriate chiral ligand was used. Subsequent reduction of the nitro group followed by hydrolysis of the oxazoline ring yielded an optically active gamma-lactam of protected alpha-quatemary serine derivative.
机译:当使用适当的手性配体时,铜催化的2-恶唑啉-和2-噻唑啉-4-羧酸的铜不对称共轭加成反应以高对映体过量选择性地产生了顺式或反加合物。随后硝基的还原,然后恶唑啉环的水解,产生了被保护的α-季铵丝氨酸衍生物的光学活性γ-内酰胺。

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