One-pot highly diastereoselective synthesis of some novel spiro pyrrolizidines via 1,3-dipolar cycloaddition reaction of azomethine ylide-Reference-Cited by-同舟云学术

One-pot highly diastereoselective synthesis of some novel spiro pyrrolizidines via 1,3-dipolar cycloaddition reaction of azomethine ylide

Published:2004-05 Issue:5 Volume:2004 Page:347-349
ISSN:1747-5198
Container-title:Journal of Chemical Research
language:en
Short-container-title:Journal of Chemical Research

Author:

Azizian Javad¹,Karimi Ali Reza¹,Dastkhan R.¹,Mohammadi Ali A.¹,Mohammadizadeh Mohammad R.¹

Affiliation:

1. Department of Chemistry, Faculty of Science, Shahid Beheshti University, PO Box 19395-4716, Tehran, Iran

Abstract

Indenoquinoxaline-11-one derivatives react with proline and N-aryl maleimides via decarboxylative azomethine ylide formation and subsequent 1,3-dipolar cycloaddition involving an exo- transition state to give new heterocyclic adducts in 71–94% yields.

Publisher

SAGE Publications

Subject

General Chemistry

Link

http://journals.sagepub.com/doi/pdf/10.3184/0308234041639872

Reference27 articles.

1. Pyrrolizidine and Indolizidine Syntheses Involving 1,3-Dipolar Cycloadditions

2. Asymmetric 1,3-Dipolar Cycloaddition Reactions

3. Recent Advances in Azomethine Ylide Chemistry

4. DNA Cross-Linking by a Phototriggered Dehydromonocrotaline Progenitor

5. Pyrrolizidine alkaloids

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