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首页> 外文期刊>Journal of Organometallic Chemistry >Oxazolidinones as chiral auxiliaries in asymmetric aldol reaction applied to natural products total synthesis
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Oxazolidinones as chiral auxiliaries in asymmetric aldol reaction applied to natural products total synthesis

机译:月唑烷酮作为手性助剂在非对称的醛醇反应中适用于天然产物的总合成

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摘要

The aldol condensation is one of the most important C-C bond formation strategies in the art of organic synthesis. Its asymmetric variant, so-called, aldol reaction has found several applications, particularly in the total synthesis of natural products. One of the most frequent and reliable application of asymmetric aldol reaction is based on the use of a chiral auxiliary. Among different readily accessible chiral auxiliaries, optically active oxazolidinones are prevalent. In 2014, we reviewed the applications of oxazolidinones as chiral auxiliaries in asymmetric aldol reactions, applied to the total synthesis of natural products. Very recently, literature survey revealed several numbers of related publications, encouraged us to update our previous review. thus in this review, we try to underscore the vital role of oxazolidinones as chiral auxiliaries in asymmetric aldol reactions as applied to the total synthesis of natural products, from 2014 to date. (C) 2020 Elsevier B.V. All rights reserved.
机译:羟醛缩合是有机合成技术中最重要的C-C键形成策略之一。它的不对称变体,即所谓的aldol反应,已经发现了一些应用,尤其是在天然产物的全合成中。不对称羟醛缩合反应最常见、最可靠的应用之一是基于手性助剂的使用。在各种容易获得的手性助剂中,光学活性恶唑烷酮是最常见的。2014年,我们回顾了恶唑烷酮作为手性助剂在不对称aldol反应中的应用,并将其应用于天然产物的全合成。最近,文献调查发现了一些相关出版物,鼓励我们更新之前的评论。因此,在这篇综述中,我们试图强调从2014年到现在,恶唑烷酮作为手性助剂在不对称羟醛缩合反应中的重要作用,并将其应用于天然产物的全合成。(C) 2020爱思唯尔B.V.版权所有。

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