Pyrrole ring opening – pyridine ring closure: Recyclization of 2-(2-oxo-1,2-dihydro-3H-pyrrol-3-ylidene)malononitriles into highly functionalized nicotinonitriles-Reference-Cited by-同舟云学术

Pyrrole ring opening – pyridine ring closure: Recyclization of 2-(2-oxo-1,2-dihydro-3H-pyrrol-3-ylidene)malononitriles into highly functionalized nicotinonitriles

Published:2020-01 Issue:2 Volume:61 Page:151368
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Milovidova Angelina G.,Belikov Mikhail Yu.,Ievlev Mikhail Yu.,Ershov Oleg V.,Nasakin Oleg E.,Tafeenko Viktor A.

Funder

RFBR

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference25 articles.

1. Metal-Free Multicomponent Syntheses of Pyridines

2. A Review: Synthesis and Medicinal Importance of Nicotinonitriles and Their Analogous

3. Discovery of trisubstituted nicotinonitrile derivatives as novel human GCN5 inhibitors through AlphaScreen-based high throughput screening

4. Recent Progress on Nicotinonitrile Scaffold-based Anticancer, Antitumor, and Antimicrobial Agents: A Literature Review

5. Design, Synthesis, and Biological Evaluation of the Third Generation 17-Cyclopropylmethyl-3,14β-dihydroxy-4,5α-epoxy-6β-[(4′-pyridyl)carboxamido]morphinan (NAP) Derivatives as μ/κ Opioid Receptor Dual Selective Ligands

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