Dipolar cycloaddition reactions in organic synthesis : synthesis of some new n-arylphthalimides and fully substituted pyrrolo [3,4 -h] quinolin derivatives
Joint Authors
al-Shirai, Abd Allah Abd al-Karim
Khalifa, Fathi A. M.
Source
Issue
Vol. 2007, Issue 13 (31 May. 2007)8 p.
Publisher
Publication Date
2007-05-31
Country of Publication
Yemen
No. of Pages
8
Main Subjects
Topics
Abstract EN
N-Arylphthalimides 3a-e were prepared through the reaction of 2-amino-3-cyano-4- ethoxycarbonyl-5-methylfuran 1 and N-Arylmaleimides 2a-e.
Compounds 3a-e reacted with malononitrile, cyanoacetophenone, cyanothioacetamide and ethylcyanoacetate to give the corresponding pyrrolo [3,4-h] quinoline derivatives 4a-e, 5a-e, 6a-e and 7a-e respectively.
The structure of the newly synthesized compounds was established on the basis of elemental analysis and spectral data studies.
American Psychological Association (APA)
al-Shirai, Abd Allah Abd al-Karim& Khalifa, Fathi A. M.. 2007. Dipolar cycloaddition reactions in organic synthesis : synthesis of some new n-arylphthalimides and fully substituted pyrrolo [3,4 -h] quinolin derivatives. al-Bāḥith al-Jāmiʻī،Vol. 2007, no. 13.
https://search.emarefa.net/detail/BIM-238361
Modern Language Association (MLA)
al-Shirai, Abd Allah Abd al-Karim& Khalifa, Fathi A. M.. Dipolar cycloaddition reactions in organic synthesis : synthesis of some new n-arylphthalimides and fully substituted pyrrolo [3,4 -h] quinolin derivatives. al-Bāḥith al-Jāmiʻī No. 13 (May. 2007).
https://search.emarefa.net/detail/BIM-238361
American Medical Association (AMA)
al-Shirai, Abd Allah Abd al-Karim& Khalifa, Fathi A. M.. Dipolar cycloaddition reactions in organic synthesis : synthesis of some new n-arylphthalimides and fully substituted pyrrolo [3,4 -h] quinolin derivatives. al-Bāḥith al-Jāmiʻī. 2007. Vol. 2007, no. 13.
https://search.emarefa.net/detail/BIM-238361
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-238361