Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3254
Title: Ruthenium(II)-Catalyzed Redox-Neutral Oxidative Cyclization of Benzimidates with Alkenes with Hydrogen Evolution
Authors: Manikandan, Rajendran
Tamizmani, Masilamani
JEGANMOHAN, MASILAMANI
Dept. of Chemistry
Keywords: Redox-Neutral Oxidative
Cyclization
Hydrogen Evolution
DFT calculations
Nitrogen-containing heterocycles
2017
Issue Date: Dec-2017
Publisher: American Chemical Society
Citation: Organic Letters, 19 (24), 6678-6681.
Abstract: 1H-Isoindoles and 2H-isoindoles are synthesized via a ruthenium-catalyzed oxidant-free cyclization of benzimidates with alkenes at room temperature with the liberation of H2. Later, 1H-isoindoles were converted into nitrogen-containing heterocycles. The proposed reaction mechanism was strongly supported by experimental evidence and DFT calculations.
URI: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3254
https://doi.org/10.1021/acs.orglett.7b03405
ISSN: 1523-7060
1523-7052
Appears in Collections:JOURNAL ARTICLES

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