Chemoselective synthesis of m-teraryls through ring transformation of 2H-pyran-2-ones by 2-(1-arylethylidene)-malononitriles-Reference-Cited by-同舟云学术

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Chemoselective synthesis of m-teraryls through ring transformation of 2H-pyran-2-ones by 2-(1-arylethylidene)-malononitriles

Published:2018 Issue:46 Volume:16 Page:8994-9002
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Panwar Rahul¹²³⁴,Shally Shally¹²³⁴,Shaw Ranjay¹²³⁴,Elagamy Amr¹²³⁴,Pratap Ramendra¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. University of Delhi

3. Delhi

4. India-110007

Abstract

Base mediated chemoselective synthesis of m-teraryls was carried out by the reaction of 2H-pyran-2-ones and 2-(1-arylethylidene)malononitriles.

Funder

University Grants Commission

Council for Scientific and Industrial Research

Department of Biotechnology, Ministry of Science and Technology

Indian Council of Medical Research

Department of Science and Technology, Ministry of Science and Technology

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB02370K

Reference96 articles.

1. Ueber die Condensation von aromatischen Aldehyden mit Cyanacetamid, Malonamid und Malonitril

2. Dual-Function Cinchona Alkaloid Catalysis: Catalytic Asymmetric Tandem Conjugate Addition−Protonation for the Direct Creation of Nonadjacent Stereocenters

3. Asymmetric Organocatalytic Double-Conjugate Addition of Malononitrile to Dienones: Efficient Synthesis of Optically Active Cyclohexanones

4. Highly Enantioslective Synthesis of Multisubstituted Polyfunctional Dihydropyrrole via an Organocatalytic Tandem Michael/Cyclization Sequence

5. Study on the Pd/C-Catalyzed (Retro-)Michael Addition Reaction of Activated Methylene Compounds to Electron-Poor Styrenes

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