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- W2950350152 abstract "Organic synthesis under solvent free conditions is imperative to develop benign chemical technologies. Among various alternatives such as use of water, ionic liquid, supercritical and liquid carbon dioxide, polyethylene and polypropylene glycol, the most convenient one is without using any solvent, so called ‘solventless reaction’ 1 . Catalyst free reactions also lead to new environmentally benign methodologies that save scarce resources. Solvent-free and catalyst free reactions possess additional advantages over conventional reactions as they not only reduce the load of effluents, but also eliminate the detrimental consequences that are inherited with them. On the other hand, selective reduction of nitroolefinic double bond in preference to nitro group is of great interest due to the potential value of corresponding nitroalkanes as they can be converted into a diverse range of compounds of biological and industrial interest through the transformation of nitro functionality into carbonyl 2 , amino 3 , oxime 4 and substitution with hydrogen 5 . The reduction of" @default.
- W2950350152 created "2019-06-27" @default.
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- W2950350152 date "2011-03-01" @default.
- W2950350152 modified "2023-09-23" @default.
- W2950350152 title "Note Catalyst-free and solventless Hantzsch ester mediated reduction of nitroolefins at elevated temperature" @default.
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- W2950350152 hasPublicationYear "2011" @default.
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