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Microwave-assisted telescoped cross metathesis-ring closing aza-Michael reaction sequence: step-economical access to nicotine-lobeline hybrid analogues

机译:微波辅助伸缩交叉复分离环关闭AZA-MICHAEL反应顺序:步进 - 经济进入尼古丁 - 叶列杂交类似物

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摘要

A series of 2,5-disubstituted pyrrolidines was synthesized through an efficient telescoped cross-metathesis/cyclizing aza-Michael addition involving N-heteroaromatic olefinic derivatives. This synthetic route was applied to the preparation of original nicotine-lobeline, nicotine-pelletierine and lobeline-nicotine-epibatidine hybrids.
机译:通过涉及N-杂芳烯烃衍生物的有效伸缩的交叉复分解/环化AZA-MICHAEL添加,合成了一系列2,5-二取代的吡咯。 将该合成途径应用于原始尼古丁 - 鳞片,尼古丁 - 薄树和尼古丁 - 尼古丁杂交物的制备。

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  • 来源
    《RSC Advances》 |2015年第117期|共5页
  • 作者单位

    Univ Paris 11 Equipe Chim Subst Nat BioCIS Univ Paris Saclay F-92296 Chatenay Malabry France;

    Univ Paris 11 Equipe Chim Subst Nat BioCIS Univ Paris Saclay F-92296 Chatenay Malabry France;

    Univ Paris 11 Equipe Chim Subst Nat BioCIS Univ Paris Saclay F-92296 Chatenay Malabry France;

    Univ Paris 11 Equipe Chim Subst Nat BioCIS Univ Paris Saclay F-92296 Chatenay Malabry France;

    Univ Paris 11 Equipe Chim Subst Nat BioCIS Univ Paris Saclay F-92296 Chatenay Malabry France;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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