A 1,3-dipolar cycloaddition of alicyclic methylene iminium ylide to form pyrrolizidine nuclei and its application to synthesis of pyrrolizidine alkaloids.
Author:
Publisher
Pharmaceutical Society of Japan
Subject
Drug Discovery,General Chemistry,General Medicine
Link
http://www.jstage.jst.go.jp/article/cpb1958/30/9/30_9_3167/_pdf
Cited by 33 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. N-(silylmethyl)amines, -amides, and -amino acids: biological activity and prospects in drug synthesis;Russian Chemical Bulletin;2011-04
2. A novel regio- and stereo-specific hydrohalogenation reaction of 2-alkynoic acids and their derivatives;Chinese Journal of Chemistry;2010-08-27
3. Osmium(II)-, Rhenium(I)-, and Tungsten(0)-Promoted Dipolar Cycloaddition Reactions with Pyrroles: Exploiting the Azomethine Ylide Character of This Heterocycle;Organometallics;2006-09-14
4. Silylmethylamines and Their Derivatives: Chemistry and Biological Activities;Advances in Organometallic Chemistry;2004
5. N-Benzyl-N-methoxymethyl-N-(trimethylsilyl)methylamine as an Azomethine Ylide Equivalent: 2,6-dioxo-1-phenyl-4-benzyl-1,4-diazabicyclo[3.3.0]octane;Organic Syntheses;2003-04-28
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