...
首页> 外文期刊>Bulletin of the Chemical Society of Japan >Synthesis of Fragment A Derivative of an Antibiotic, Nosiheptide
【24h】

Synthesis of Fragment A Derivative of an Antibiotic, Nosiheptide

机译:抗生素Nosiheptide片段A衍生物的合成

获取原文
获取原文并翻译 | 示例
           

摘要

Two 4-ethoxycarbonyl thiazolyl groups were introduced into 2- and 5-positions of 3-hydroxypyridine in 8 steps using 5-cyano-3-hydroxypyridine (2) as the staring materials. The pyridine derivative obtained in the last step was converted to a fragment A derivative (21) by stepwise introduction of the 2-substituted 4-thiazolyl group into the 6-position. The total yield for the formation of 21 via 14 steps was 7.6%
机译:以5-氰基-3-羟基吡啶(2)为起始原料,分8步将两个4-乙氧基羰基噻唑基引入3-羟基吡啶的2-和5-位。通过将2-取代的4-噻唑基逐步引入6-位,将在最后一步中获得的吡啶衍生物转化为片段A衍生物(21)。通过14个步骤形成21个步骤的总收率为7.6%

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