首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >QUASSINOID SUPPORT STUDIES:INCREASING STEREOCONTROL IN A PERHYDRONAPHTHALENE SYNTHESIS BY RESTRICTING CONFORMATIONAL DEGREES OF FREEDOM
【24h】

QUASSINOID SUPPORT STUDIES:INCREASING STEREOCONTROL IN A PERHYDRONAPHTHALENE SYNTHESIS BY RESTRICTING CONFORMATIONAL DEGREES OF FREEDOM

机译:类肌醇的支持研究:通过限制构象自由度来增强邻苯二甲萘合成中的立体控制

获取原文
获取原文并翻译 | 示例
           

摘要

Free radical cyclization of 15 provides trans-perhydronaphthalene (16) in high yield and with much better stereoselectivity than conformationally less constrained analogs.The quassinoids are a large family of terpenoid natural products exemplified by chaparrinone (l).1 The quassinoids have been of long-standing interest to the medicinal chemistry community because of their broad biological activities.
机译:15的自由基环化可提供高收率的反式全氢萘(16),其立体选择性比构象上受限制较少的类似物更好。拟南芥类是萜类天然产物的一大家族,例如查帕瑞酮(l)。1拟南芥很长由于其广泛的生物活性而对药物化学界具有浓厚的兴趣。

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