Synthesis of 2‐(2H‐Chromenyl)‐Oxazoles from 2H‐Chromene Hemiacetals by Using a Modified Passerini‐Type Reaction,ChemistrySelect

当前位置： X-MOL 学术 › ChemistrySelect › 论文详情

Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)

Synthesis of 2‐(2H‐Chromenyl)‐Oxazoles from 2H‐Chromene Hemiacetals by Using a Modified Passerini‐Type Reaction
ChemistrySelect ( IF 1.9 ) Pub Date : 2018-09-06 , DOI: 10.1002/slct.201802363
Deng-Ming Huang ₁ , Hui-Jing Li ₁ , Quanfu Wang ₁ , Peisheng Yan ₁ , Yan-Chao Wu _{1,

2}

Affiliation

A modified Passerini‐type reaction has been developed for the facile synthesis of 2‐(2H‐chromenyl)‐oxazoles, in which 2H‐chromene hemiacetals instead of the usually used aldehydes were adopted as the key substrates. Derivation of a 2‐(2H‐chromenyl)‐oxazole to the respective 2H‐chromene peptide and 1‐(2H‐chromenyl)‐furan was further accomplished.

中文翻译：

使用改良的Passerini型反应从2H-Chromene半缩醛合成2-（2H-Chromenyl）-Oxazoles

已开发出一种改良的Passerini型反应物，可轻松合成2-（2 H-苯二甲基）-恶唑，其中采用2 H-色烯半缩醛代替常用的醛作为关键底物。进一步完成了将2-（2 H-色烯基）-恶唑衍生为各自的2 H-色烯肽和1-（2 H-色烯基）-呋喃。

更新日期：2018-09-06

点击分享查看原文

点击收藏

阅读更多本刊最新论文本刊介绍/投稿指南11