General Synthesis of 1-Aryl-6-azaisocytosines and Their Utilization for the Preparation of Related Condensed 1,2,4-Triazines.

Clicks: 330
ID: 64056
2019
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal
Emerging

Ranked #311 of 729 articles by views in molecules

Most read Least read

Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 729 in total.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Sign in to mint
Abstract
A simple general synthesis of 1-aryl-6-azaisocytosine-5-carbonitriles is described. This method is based on coupling diazonium salts with cyanoacetylcyanamide and then cyclization of the formed 2-arylhydrazono-2-cyanoacetylcyanamides . The 6-azaisocytosines were studied with respect to tautomeric equilibrium and the transformation of functional groups, and used in the synthesis of the condensed heterocyclic compounds: Purine isosteric imidazo[2,1-]-[1,2,4]triazine and the 1,2,4-triazino[2,3-]quinazolines -.
Reference Key
zlek2019generalmolecules Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors František Zálešák, Jan Slouka, Jakub Stýskala
Are you one of these authors? Claim your profile
Journal molecules
Year 2019
DOI
E3558
URL
Keywords
1,2,4-triazine 1-aryl-6-azaisocytosine condensed 1,2,4-triazine cyclization of arylhydrazones fused azaisocytosines

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

Comments

No comments yet. Be the first to comment on this article.