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Asymmetric aza-Henry reaction with α-substituted nitroacetates catalyzed by a bifunctional thiourea-guanidine catalyst

机译:双官能硫脲-胍催化剂催化的α-取代硝基乙酸酯的不对称氮杂-亨利反应

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摘要

The asymmetric aza-Henry reaction of α-substituted nitroacetates and N-Boc imines was achieved with a new-type thiourea-guanidine bifunctional organocatalyst. The novel transformations exhibited high diastereoselectivities, and the adducts bearing adjacent quaternary and tertiary chiral centers were generally obtained in moderate to good enantioselectivities (up to 88% ee).
机译:用新型硫脲-胍双官能团有机催化剂实现了α-取代的硝基乙酸酯和N-Boc亚胺的不对称氮杂-亨利反应。新的转化表现出高的非对映选择性,并且带有相邻的季和三级手性中心的加合物通常以中等至良好的对映选择性(高达88%ee)获得。

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  • 来源
    《中国化学快报(英文版)》 |2011年第8期|923-926|共4页
  • 作者单位

    State Key Laboratory Breeding Base of Systematic Research, Development and Utilization of Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China;

    State Key Laboratory Breeding Base of Systematic Research, Development and Utilization of Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China;

    State Key Laboratory of Oral Diseases, Department of Orthodontics, West China College of Stomatolgy, Sichuan University, Chengdu 610041, China;

    State Key Laboratory Breeding Base of Systematic Research, Development and Utilization of Chinese Medicine Resources, School of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 chi
  • 中图分类
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  • 入库时间 2024-01-27 01:26:45
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