Metal-free transfer hydrogenation/cycloaddition cascade of activated quinolines and isoquinolines with tosyl azides-Reference-Cited by-同舟云学术

Metal-free transfer hydrogenation/cycloaddition cascade of activated quinolines and isoquinolines with tosyl azides

Published:2023 Issue:46 Volume:59 Page:7088-7091
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Yadav Suman¹,Kant Ruchir²,Kuram Malleswara Rao¹³^ORCID

Affiliation:

1. Medicinal and Process Chemistry Division, CSIR-Central Drug Research Institute, Lucknow 226031, India

2. MSB Division, CSIR-Central Drug Research Institute, Lucknow 226031, India

3. Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India

Abstract

The intrinsically unstable cyclic enamines impeded for exploration in cycloaddition reaction. Here, we accomplished a cascade reaction providing cyclic amidines by the cycloaddition of azides with in situ generated enamines.

Funder

Science and Engineering Research Board

University Grants Commission

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2023/CC/D3CC01430D

Reference35 articles.

1. Progress in the Chemistry of Tetrahydroquinolines

2. Highly Potent and Selective Dopamine D₄ Receptor Antagonists Potentially Useful for the Treatment of Glioblastoma

3. Advances in the Chemistry of Tetrahydroquinolines

4. Synthesis and Biological Evaluation of a Novel Series of Heterobivalent Muscarinic Ligands Based on Xanomeline and 1-[3-(4-Butylpiperidin-1-yl)propyl]-1,2,3,4-tetrahydroquinolin-2-one (77-LH-28-1)

5. Sequential and direct multicomponent reaction (MCR)-based dearomatization strategies

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