首页> 外文期刊>Organic letters >L-proline-catalyzed direct intermolecular asymmetric aldol reactions of 1-phenylthiocycloalkyl carboxaldehydes with ketones. Easy access to spiro- and fused-cyclobutyl tetrahydrofurans and cyclopentanones
【24h】

L-proline-catalyzed direct intermolecular asymmetric aldol reactions of 1-phenylthiocycloalkyl carboxaldehydes with ketones. Easy access to spiro- and fused-cyclobutyl tetrahydrofurans and cyclopentanones

机译:L-脯氨酸催化的1-苯基硫代环烷基羧醛与酮的直接分子间不对称醛醇缩合反应。容易获得螺和稠环丁基四氢呋喃和环戊酮

获取原文
获取原文并翻译 | 示例
           

摘要

Acid-catalyzed ring expansion of chiral cyclopropyl and cyclobutyl derivatives for the synthesis of carbo- and heterocyclic compounds is reported. The starting materials have been successfully prepared by l-proline-catalyzed direct asymmetric aldol reactions of 1-phenylthiocycloalkyl carboxaldehydes with ketones.
机译:报道了用于合成碳和杂环化合物的手性环丙基和环丁基衍生物的酸催化扩环。通过1-脯氨酸催化1-苯基硫代环烷基羧醛与酮的直接不对称醛醇缩合反应已成功制备了起始原料。

著录项

相似文献

  • 外文文献
  • 中文文献
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