Lewis acid-promoted direct synthesis of N-unsubstituted hydrazones via the reaction of hydrazine with acetophenone and isatin derivatives


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Abstract

Hydrazones 2–22 were synthesized via the reaction of acetophenone with isatin derivatives and anhydrous hydrazine promoted by BF3 as a Lewis acid at 0°C. Structures of the synthesized hydrazones were determined on the basis of NMR and X-ray crystallographic analyses.

About the authors

A. S. El-Azab

Department of Pharmaceutical Chemistry, College of Pharmacy; Department of Organic Chemistry, Faculty of Pharmacy

Author for correspondence.
Email: adelazaba@yahoo.com
Saudi Arabia, Riyadh, 11451; Cairo

H. A. Ghabbour

Department of Pharmaceutical Chemistry, College of Pharmacy; Department of Medicinal Chemistry, Faculty of Pharmacy

Email: adelazaba@yahoo.com
Saudi Arabia, Riyadh, 11451; Mansoura, 35516

W. M. El-Husseiny

Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy

Email: adelazaba@yahoo.com
Egypt, Mansoura, 35516

A. R. Maarouf

Department of Medicinal Chemistry, Faculty of Pharmacy; Department of Pharmaceutical Chemistry, College of Pharmacy

Email: adelazaba@yahoo.com
Egypt, Mansoura, 35516; Gamasa City

M. A. Mohamed

Department of Organic Chemistry, Faculty of Pharmacy; Department of Pharmaceutical Chemistry, College of Pharmacy

Email: adelazaba@yahoo.com
Egypt, Cairo; AlKharj

A. A.-M. Abdel-Aziz

Department of Pharmaceutical Chemistry, College of Pharmacy; Department of Medicinal Chemistry, Faculty of Pharmacy

Email: adelazaba@yahoo.com
Saudi Arabia, Riyadh, 11451; Mansoura, 35516

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