The reactions of 1,3-dipolar ketazines with dipolarophile acetylene derivatives

Dissertant

al-Tarawinah, Musa Ata Allah

Thesis advisor

al-Alaali, Abd Allah Muhammad

Comitee Members

al-Tawil, Samir Ahmad
al-Mahasinah, Ali Shakir

University

Mutah University

Faculty

Faculty of Science

Department

Department of Chemistry

University Country

Jordan

Degree

Master

Degree Date

2002

English Abstract

Some aromatic ketazines, which are actually, heterodynes ; reacted here not as 1,3-heterodienes in [4+2]-cycloaddition but as 1,3-dipolai compounds.

Their reactions with two moles of dimethyl acetylene carboxylate, led to [3 + 2]-cycloaddition reactions.

Theist reactions and due to the nature of ketones used gave two different azine products, namely, bicyclic azine and acyclic azine.

Characterization the products was achieved by H-NMR, C-NMR, IR- spectroscopy an elemental analysis.

Main Subjects

Chemistry

Topics

No. of Pages

73

Table of Contents

Table of contents.

Abstract.

Chapter one : Introduction.

Chapter two : Results and discussion.

Chapter three : Experimental.

Chapter four : Summary and conclusion.

References.

American Psychological Association (APA)

al-Tarawinah, Musa Ata Allah. (2002). The reactions of 1,3-dipolar ketazines with dipolarophile acetylene derivatives. (Master's theses Theses and Dissertations Master). Mutah University, Jordan
https://search.emarefa.net/detail/BIM-304535

Modern Language Association (MLA)

al-Tarawinah, Musa Ata Allah. The reactions of 1,3-dipolar ketazines with dipolarophile acetylene derivatives. (Master's theses Theses and Dissertations Master). Mutah University. (2002).
https://search.emarefa.net/detail/BIM-304535

American Medical Association (AMA)

al-Tarawinah, Musa Ata Allah. (2002). The reactions of 1,3-dipolar ketazines with dipolarophile acetylene derivatives. (Master's theses Theses and Dissertations Master). Mutah University, Jordan
https://search.emarefa.net/detail/BIM-304535

Language

English

Data Type

Arab Theses

Record ID

BIM-304535