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Chloroform as a Co Surrogate: Applications and Recent Developments

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dc.contributor.author K, Mondal
dc.contributor.author P, Halder
dc.contributor.author G, Gopalan
dc.contributor.author P, Sasikumar
dc.contributor.author K V, Radhakrishnan
dc.contributor.author P, Das
dc.date.accessioned 2020-02-26T09:01:18Z
dc.date.available 2020-02-26T09:01:18Z
dc.date.issued 2019-04-24
dc.identifier.citation Organic & Biomolecular Chemistry; 17(21):5212-5222 en_US
dc.identifier.uri https://pubs.rsc.org/en/content/articlepdf/2019/ob/c9ob00886a
dc.identifier.uri http://10.10.100.66:8080/xmlui/handle/123456789/3592
dc.description.abstract The carbonyl moiety is one of the indispensable sub-units in organic synthesis with significant applications in medicinal as well as materials chemistry. Hence the insertion of a carbonyl group via simple and highly efficient routes has been one of the most challenging tasks for organic chemists. Though the direct utilisation of CO gas in carbonylation is the fundamental procedure for the construction of carbonyl compounds, it has certain drawbacks due to its toxic and explosive nature. As a result, the need for cheap and efficient CO surrogates has gained much attention nowadays by which CO gas can be easily generated in situ or ex situ. In this review we discuss the advantages of chloroform as CO surrogate and have surveyed recent carbonylation reactions where chloroform has been used as CO source. en_US
dc.language.iso en en_US
dc.publisher Royal Society of Chemistry en_US
dc.subject carbonyl moiety en_US
dc.subject materials chemistry en_US
dc.subject carbonylation en_US
dc.subject CO surrogate en_US
dc.title Chloroform as a Co Surrogate: Applications and Recent Developments en_US
dc.type Article en_US


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  • 2019
    Research articles authored by NIIST researchers published in 2019

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