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


Citar

Texto integral

Acesso aberto Acesso aberto
Acesso é fechado Acesso está concedido
Acesso é fechado Somente assinantes

Resumo

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.

Sobre autores

A. El-Azab

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

Autor responsável pela correspondência
Email: adelazaba@yahoo.com
Arábia Saudita, Riyadh, 11451; Cairo

H. Ghabbour

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

Email: adelazaba@yahoo.com
Arábia Saudita, Riyadh, 11451; Mansoura, 35516

W. El-Husseiny

Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy

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

A. Maarouf

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

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

M. Mohamed

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

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

A. Abdel-Aziz

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

Email: adelazaba@yahoo.com
Arábia Saudita, Riyadh, 11451; Mansoura, 35516

Arquivos suplementares

Arquivos suplementares
Ação
1. JATS XML

Declaração de direitos autorais © Pleiades Publishing, Ltd., 2016