Lewis Acid Catalyzed Intramolecular [4+2] Cycloaddition of In Situ Generated Aza‐Quinone Methides for the Stereoselective Synthesis of Furo/pyrano[3,2‐ c ]tetrahydroquinolines-Reference-Cited by-同舟云学术

Lewis Acid Catalyzed Intramolecular [4+2] Cycloaddition of In Situ Generated Aza‐Quinone Methides for the Stereoselective Synthesis of Furo/pyrano[3,2‐ c ]tetrahydroquinolines

Published:2019-12-10 Issue:44 Volume:2020 Page:6887-6891
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Gharpure Santosh J.¹^ORCID,Vishwakarma Dharmendra S.¹^ORCID

Affiliation:

1. Department of Chemistry Indian Institute of Technology Bombay Powai 400076 Mumbai – India

Funder

Science and Engineering Research Board

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.201901598

Reference56 articles.

1. Quinoline: A promising antitubercular target

2. Natural Product Inspired Diversity Oriented Synthesis of Tetrahydroquinoline Scaffolds as Antitubercular Agent

3. Progress in the Chemistry of Tetrahydroquinolines

4. The discovery and optimization of hexahydro-2H-pyrano[3,2-c]quinolines (HHPQs) as potent and selective inhibitors of the mitotic kinesin-5

5. The first target specific, highly diastereoselective synthesis, design and characterization of pyranoquinolinyl acrylic acid diastereomers as potential α-glucosidase inhibitors

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