Author:
Mohammadizadeh Mohammad R,Azizian Javad,Teimouri Fatemeh,Mohammadi Ali A,Karimi Ali R,Tamari Esmail
Abstract
A versatile and highly efficient procedure has been introduced for preparation of spiro pyridodipyrimidines during the investigation of the reaction of 1,3-dimethyl-6- aminouracil with isatin derivatives, ninhydrin, and acenaphthoquinone under classical or microwave-assisted solvent-free conditions.Key words: isatin, ninhydrin, acenaphtoquinone, 1,3-dimethyl-6-aminouracil, solvent-free.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
18 articles.
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1. Developments of pyridodipyrimidine heterocycles and their biological activities;Molecular Diversity;2023-02-25
2. Synthesis of spiro(pyrrol-2,5'-pyrrolo[2,3-<i>d</i>]pyrimidine)2',4',5,6'-tetraones by the reaction of pyrrolo[2,1-<i>c</i>][1,4]oxazinetriones with 6-aminopyrimidine-2,4-diones;Журнал органической химии;2023-02-15
3. Synthesis of Spiro(pyrrol-2,5'-pyrrolo[2,3-d]pyrimidine)-2',4',5,6'-tetraones by the Reaction of Pyrrolo[2,1-c][1,4]oxazinetriones with 6-Aminopyrimidine-2,4-diones;Russian Journal of Organic Chemistry;2023-02
4. One-pot multi-component synthesis of diverse bioactive heterocyclic scaffolds involving 6-aminouracil or its N-methyl derivatives as a versatile reagent;Physical Sciences Reviews;2022-03-17
5. Synthesis of heterocyclic compounds via Michael and Hantzsch reactions;Journal of Heterocyclic Chemistry;2020-04