Synthesis of tetrahydro-1H-indolo[2,3-b]pyrrolo[3,2-c]quinolones via intramolecular oxidative ring rearrangement of tetrahydro-β-carbolines and their biological evaluation-Reference-Cited by-同舟云学术

Synthesis of tetrahydro-1H-indolo[2,3-b]pyrrolo[3,2-c]quinolones via intramolecular oxidative ring rearrangement of tetrahydro-β-carbolines and their biological evaluation

Published:2018 Issue:8 Volume:42 Page:6538-6547
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Bathula Chandramohan¹²³⁴⁵,Roma-Rodrigues Catarina⁶⁷⁸⁹¹⁰,Chauhan Jyoti¹²³⁴⁵,Fernandes Alexandra R.⁶⁷⁸⁹¹⁰,Sen Subhabrata¹²³⁴⁵^ORCID

Affiliation:

1. Department of Chemistry

2. School of Natural Sciences

3. Shiv Nadar University

4. GautamBudh Nagar

5. India

6. UCIBIO

7. Departamento de Ciências da Vida

8. Faculdade de Ciências e Tecnologia

9. Universidade Nova de Lisboa

10. Caparica

Abstract

Tetrahydro-1H-indolo[2,3-b]pyrrolo[3,2-c]quinolones are synthesized via a unique intramolecular oxidative ring rearrangement.

Funder

Shiv Nadar University

European Commission

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2018/NJ/C7NJ04616B

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2. Gardneria alkaloids -IX structures of chitosenine and three other minor bases

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4. Spirotryprostatin B, a Novel Mammalian Cell Cycle Inhibitor Produced by Aspergillus fumigatus.

5. Small-Molecule Inhibitors of the MDM2-p53 Protein-Protein Interaction to Reactivate p53 Function: A Novel Approach for Cancer Therapy

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