A novel access to pyrido[4,3-d]pyrimidine scaffold via Staudinger/intramolecular aza-Wittig reaction of 5-acyl-4-(β-azidoalkyl)-1,2,3,4-tetrahydropyrimidin-2-ones-Reference-Cited by-同舟云学术

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A novel access to pyrido[4,3-d]pyrimidine scaffold via Staudinger/intramolecular aza-Wittig reaction of 5-acyl-4-(β-azidoalkyl)-1,2,3,4-tetrahydropyrimidin-2-ones

Published:2014-09 Issue:35 Volume:70 Page:5398-5414
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Fesenko Anastasia A.,Shutalev Anatoly D.

Funder

Presidential Grant for Young Scientists

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference55 articles.

1. For reviews on pyridopyrimidines, see:

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1. A new approach to the pyrrolo[3,4-d] pyrimidine system via tandem Staudinger/aza-Wittig reaction of 5-acyl-4-azidomethyl-3,4-dihydropyrimidin-2(1H)-ones;Chemistry of Heterocyclic Compounds;2023-12

2. Chemistry and biological evaluation of pyrido[4,3‐ d ]pyrimidines: A review;Chemical Biology & Drug Design;2022-02-20

3. Bicyclic 6-6 Systems: Three Heteroatoms 1:2;Comprehensive Heterocyclic Chemistry IV;2022

4. Advances in the synthesis of heterocycles bearing an endocyclic urea moiety;Russian Chemical Reviews;2021-04-01

5. Synthesis, characterization and crystal structure of heterocyclic tetrahydropyrido[4′,3′:4,5]thieno[2,3-d]pyrimidinone derivatives via sequential aza-Wittig/base catalyzed cyclization;Journal of Molecular Structure;2019-03

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