Synthetic communications

Spiro-[4 H-pyrroIo [1, 2-a][1, 4] benzodiazepine-4, 4′-piperidine] Derivatives as Potential Nootropic Agents: A Simple One-Pot Synthesis

S Massa, A Mai, M Artico

Index: Massa, S.; Mai, A.; Artico, M. Synthetic Communications, 1990 , vol. 20, # 22 p. 3537 - 3545

Full Text: HTML

Citation Number: 9

Abstract

Abstract Some derivatives of a new heterocyclic ring, spiro-[4 H-pyrrolo [1, 2a][1, 4] benzodiazepine-4, 4′-piperidine], have been obtained in very good yields by a simple one- pot reaction using 1-(2-aminomethylphenyl)-1 H-pyrrole and 1-substituted 4-oxopiperidines as the synthones.

Related Articles:

Structure–activity relationships of new cyanothiophene inhibitors of the essential peptidoglycan biosynthesis enzyme MurF

[Hrast, Martina; Turk, Samo; Sosic, Izidor; Knez, Damijan; Randall, Christopher P.; Barreteau, Helene; Contreras-Martel, Carlos; Dessen, Andrea; O'Neill, Alex J.; Mengin-Lecreulx, Dominique; Blanot, Didier; Gobec, Stanislav European Journal of Medicinal Chemistry, 2013 , vol. 66, p. 32 - 45]

4-Piperidinylimino: a nearly linear head-to-tail linking group for dipolar chromophores

[Katz, H. E.; Lavell, W. T. Journal of Organic Chemistry, 1991 , vol. 56, # 7 p. 2282 - 2284]

More Articles...