Synthesis and in Vitro Cytotoxic Evaluation of New Derivatives of Pyrido[1,2-A]benzimidazolic Ring System: The Pyrido[1',2':1,2]imidazo[4,5-H]quinazolines.

Chemical and Pharmaceutical Bulletin- Japan

doi 10.1248/cpb.49.1061

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January 1, 2001

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Pharmaceutical Society of Japan

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Synthesis and in Vitro Cytotoxic Evaluation of New Derivatives of Pyrido[1,2-A]benzimidazolic Ring System: The Pyrido[1',2':1,2]imidazo[4,5-H]quinazolines.

Chemical and Pharmaceutical Bulletin- Japan

Full Text

Abstract

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Date

Authors

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Related search

Studies of Quinazoline Pigments. II. Synthesis of Dimethyl Substituted Pyrido[2,1-B]pyrido[1′,2′:1,2]pyrimido-[4,5-G]quinazoline-7,15-Diones

Stemocurtisine, the First Pyrido[1,2-A]azapineStemonaAlkaloid

One-Pot Synthesis of 2h-Quinolizine and 1h-Pyrido[1,2-A]qinoline Derivatives by Using Dialkylcarbodiimides

Synthesis of Quinazolines and Imidazo[1,2-C]quinazolines With the Aid of a Low-Valent Titanium Reagent

A Facile Pseudo Three Component Reaction for the Synthesis of Benzo [4,5]imidazo[1,2-A]pyridine Derivatives

Substituted Pyridopyrimidinones. Part III. Synthesis of Some Novel Ether Derivatives of 4h-Pyrido[1,2-A]pyrimidin-4-One

Microwave-Assisted Suzuki-Miyaura and Sonogashira Coupling of 4-Chloro-2-(Trifluoromethyl)pyrido[1,2-E]purine Derivatives

12-(4-Methoxybenzoyl)-2-Methylbenzo[f]pyrido[1,2-A]indole-6,11-Dione

New Route to Pyrido[1,2-B]pyridazinium Inner Salts. Evidence of a 1,3-Dipolar Cycloaddition-Ring Expansion Process