One-Step Synthesis of Isoindolo[2,1-a]indol-6-ones via Tandem Pd-Catalyzed Aminocarbonylation and C

One-Step Synthesis of Isoindolo[2,1-a]indol-6-ones via Tandem Pd-Catalyzed Aminocarbonylation and C–H Activation

Published:2019-09-11 Issue:19 Volume:84 Page:12499-12507
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Čarný Tomáš¹,Markovič Martin¹²^ORCID,Gracza Tibor¹^ORCID,Koóš Peter¹²^ORCID

Affiliation:

1. Department of Organic Chemistry, Institute of Organic Chemistry, Catalysis and Petrochemistry, Slovak University of Technology, Radlinského 9, SK-812 37 Bratislava, Slovakia

2. Georganics Ltd., Koreničova 1, SK-811 03 Bratislava, Slovakia

Funder

Vedeck? Grantov? Agent?ra M?VVa? SR a SAV

Agent?ra na Podporu V?skumu a V?voja

Department of Organic Chemistry, Slovenska Technicka Univerzita

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b02008

Reference41 articles.

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2. New ligands at the melatonin binding site MT3

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4. Synthesis and Antiproliferative Activity of Basic Ethers of 1,2-Dihydropyrrolo[1,2-a]indole, 6H-Isoindolo[2,1-a]indole, and 6H-Benz[5,6]isoindolo[2,1-a]indole

5. A Pd-catalyzed direct entry to 11-substituted 6H-isoindolo[2,1-a]indol-6-one derivatives as potential anticancer agents

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