...
首页> 外文期刊>Letters in Organic Chemistry >A Study of the Influence of Base, Temperature and Reaction Time in Nitroaldol Reactions Using (R)-(+)-Glyceraldehyde Acetonide: Diastereoselective Synthesis of (4R, 5R)-Dihydro-5-((R)-1,2-Dihydroxyethyl)-4-Nitrofuran- 2(3H)-one
【24h】

A Study of the Influence of Base, Temperature and Reaction Time in Nitroaldol Reactions Using (R)-(+)-Glyceraldehyde Acetonide: Diastereoselective Synthesis of (4R, 5R)-Dihydro-5-((R)-1,2-Dihydroxyethyl)-4-Nitrofuran- 2(3H)-one

机译:碱,温度和反应时间对使用(R)-(+)-甘油醛乙醛的硝基羟醛反应的影响的研究:(4R,5R)-Dihydro-5-((R)-1,2-Dihydroxyethyl)的非对映选择性合成)-4-硝基呋喃-2(3H)-一

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The Henry reaction between the nitroalkanes 6-11 and (R)-(+)-glyceraldehyde acetonide (1), was investigated in respect to the variation of the base, temperature and reaction time. Nitroalcohols 5a-f were obtained in good yields (70- 85%) and moderate to good anti-selectivities (50-79%). The transformation of the nitroalcohol 5a,b in title γ-lactone 2, a potential precursor of bioactive β-aminoacids, was also investigated.
机译:研究了碱,温度和反应时间的变化,研究了硝基烷6-11与(R)-(+)-甘油醛丙酮化物(1)之间的亨利反应。以良好的收率(70-85%)和中等至良好的抗选择性(50-79%)获得了硝基醇5a-f。还研究了标题γ-内酯2中的硝基醇5a,b的转化,后者是生物活性β-氨基酸的潜在前体。

著录项

相似文献

  • 外文文献
  • 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