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Synthesis of functionalized oxazolidines by multicomponent reactions of 1,2-amino alcohols (microreview)
Chemistry of Heterocyclic Compounds ( IF 1.4 ) Pub Date : 2020-05-04 , DOI: 10.1007/s10593-020-02681-w Xianjun Xu , Hua Wei , Huangdi Feng
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Recent (2011–2019) multicomponent syntheses of functionalized oxazolidines using 1,2-amino alcohols as starting materials are reviewed. The synthetic strategies are gathered into three groups: metal-free domino annulation/Mannich reactions, transition metal-catalyzed cascade reactions, extended one-pot asymmetric azaelectrocyclization.![](//media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-020-02681-w/MediaObjects/10593_2020_2681_Figd_HTML.jpg)
中文翻译:
通过1,2-氨基醇的多组分反应合成官能化的恶唑烷(microreview)
![](//media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-020-02681-w/MediaObjects/10593_2020_2681_Figb_HTML.jpg)
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综述了近期(2011–2019年)以1,2-氨基醇为原料的功能化恶唑烷的多组分合成。合成策略分为三类:无金属的多米诺环化/曼尼希反应,过渡金属催化的级联反应,扩展的一锅式不对称氮杂电环化。![](//media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-020-02681-w/MediaObjects/10593_2020_2681_Figd_HTML.jpg)
更新日期:2020-05-04
Chemistry of Heterocyclic Compounds ( IF 1.4 ) Pub Date : 2020-05-04 , DOI: 10.1007/s10593-020-02681-w Xianjun Xu , Hua Wei , Huangdi Feng
![](http://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-020-02681-w/MediaObjects/10593_2020_2681_Figb_HTML.jpg)
![](http://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-020-02681-w/MediaObjects/10593_2020_2681_Figc_HTML.jpg)
![](http://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-020-02681-w/MediaObjects/10593_2020_2681_Figd_HTML.jpg)
中文翻译:
![](https://static.x-mol.com/jcss/images/paperTranslation.png)
通过1,2-氨基醇的多组分反应合成官能化的恶唑烷(microreview)
![](http://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-020-02681-w/MediaObjects/10593_2020_2681_Figb_HTML.jpg)
![](http://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-020-02681-w/MediaObjects/10593_2020_2681_Figc_HTML.jpg)
![](http://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs10593-020-02681-w/MediaObjects/10593_2020_2681_Figd_HTML.jpg)