首页> 外文期刊>Tetrahedron >Stereoselective preparation of trifluoromethyl containing 1,4-oxathiolane derivatives through ring expansion reaction of 1,3-oxathiolanes
【24h】

Stereoselective preparation of trifluoromethyl containing 1,4-oxathiolane derivatives through ring expansion reaction of 1,3-oxathiolanes

机译:通过1,3-氧杂硫杂环戊烷的扩环反应立体选择性地制备含三氟甲基的1,4-氧杂硫杂环戊烷衍生物

获取原文
获取原文并翻译 | 示例
           

摘要

Trifluoromethyl containing 1,4-oxathiolanes are synthesized in excellent yields and high stereoselectivities from the expansion reactions of sulfur ylide intermediates, which were prepared from the reaction of 2-diazo-3,3,3-trifluoro-propionic acid methyl ester and 1,3-oxathiolanes in the presence of Rh-2(OAc)(4), (c) 2005 Elsevier Ltd. All rights reserved.
机译:含有三氟甲基的1,4-氧杂硫杂环戊烷是由硫叶立德中间体的膨胀反应以高收率和高立体选择性合成的,后者是由2-重氮3,3,3-三氟丙酸甲酯与1,在Rh-2(OAc)(4),(c)2005 Elsevier Ltd.存在下的3-氧杂硫杂环戊烷。保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号