Synthesis of the first 4-oxobutane-1,1,2,2-tetracarbonitriles containing a phenol fragment and their transformation into cyano-substituted pyrrol-2-ones showing three-position molecular switching-Reference-Cited by-同舟云学术

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Synthesis of the first 4-oxobutane-1,1,2,2-tetracarbonitriles containing a phenol fragment and their transformation into cyano-substituted pyrrol-2-ones showing three-position molecular switching

Published:2024 Issue:23 Volume:22 Page:4757-4765
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Belikov Mikhail Yu.¹^ORCID,Milovidova Angelina G.¹^ORCID,Ievlev Mikhail Yu.¹^ORCID,Fedoseev Sergey V.¹^ORCID

Affiliation:

1. Ulyanov Chuvash State University, Moskovsky pr., 15, Cheboksary, Russia

Abstract

A new branch of diversity-oriented synthesis based on nitrile-rich substrates was discovered. The preparation of switchable multicolor pyrrole derivatives was shown.

Funder

Russian Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/OB/D4OB00612G

Reference49 articles.

1. Complexity‐to‐Diversity and Pseudo‐Natural Product Strategies as Powerful Platforms for Deciphering Next‐Generation Therapeutics

2. Natural product-inspired strategies towards the discovery of novel bioactive molecules

3. Medium-Sized Ring Expansion Strategies: Enhancing Small-Molecule Library Development

4. Recent achievements and current trajectories of diversity-oriented synthesis

5. Diversity-oriented synthesis as a tool for the discovery of novel biologically active small molecules

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