Enantioselective Synthesis of 3‐Amino‐3’‐carbazole Oxindole Derivatives via Friedel‐Crafts Aminoalkylation Reaction-Reference-Cited by-同舟云学术

Enantioselective Synthesis of 3‐Amino‐3’‐carbazole Oxindole Derivatives via Friedel‐Crafts Aminoalkylation Reaction

Published:2022-02-17 Issue:7 Volume:7 Page:
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Muthusamy Subramaniam¹^ORCID,Kumarswamyreddy Nandarapu²^ORCID,Kesavan Venkitasamy¹^ORCID

Affiliation:

1. Chemical Biology Laboratory Department of Biotechnology Bhupat and Jyothi Mehta School of Biosciences Building Indian Institute of Technology Madras Chennai 600036 India

2. Department of Chemistry Indian Institute of Technology Tirupati Tirupati 517506 Andhra Pradesh India

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.202200131

Reference85 articles.

2. Biologically active isoquinoline alkaloids covering 2014–2018

3. Prescribed drugs containing nitrogen heterocycles: an overview

4. Total Synthesis of Hamigerans: Part 1. Development of Synthetic Technology for the Construction of Benzannulated Polycyclic Systems by the Intramolecular Trapping of Photogenerated Hydroxy-o-quinodimethanes and Synthesis of Key Building Blocks This work was financially supported by the National Institutes of Health (USA) and The Skaggs Institute for Chemical Biology, and grants from Abbott, Amgen, ArrayBiopharma, Boehringer-Ingelheim, Glaxo, Hoffmann-La Roche, DuPont, Merck, Pfizer, and Schering Plough.

5. The Impact of Alkaloids Structures from NaturalCompounds on Public Health

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