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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kshirsagar, Umesh Achyutrao | en_US |
dc.date.accessioned | 2022-03-17T01:00:00Z | - |
dc.date.accessioned | 2022-03-21T11:29:45Z | - |
dc.date.available | 2022-03-17T01:00:00Z | - |
dc.date.available | 2022-03-21T11:29:45Z | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | Kshirsagar, U. A., Waghmare, D. S., & Tambe, S. D. (2020). The regioselective coupling of 2-arylquinazolinone C-H with aldehydes and benzyl alcohols under oxidative conditions. New Journal of Chemistry, 44(39), 16697-16701. doi:10.1039/d0nj03721d | en_US |
dc.identifier.issn | 1144-0546 | - |
dc.identifier.other | EID(2-s2.0-85093503457) | - |
dc.identifier.uri | https://doi.org/10.1039/d0nj03721d | - |
dc.identifier.uri | https://dspace.iiti.ac.in/handle/123456789/8770 | - |
dc.description.abstract | The direct and regioselective palladium-catalyzed dehydrogenative coupling of aldehydes and benzyl alcohols with 2-aryl-quinazolinone C-H endowed with a quinazolinone nucleus, which is one of the most fascinating and vital core units, as an inherent directing group under oxidative conditions was developed. This atom/step economic aroylation offers an attractive handle and a very green approach for highly convergent and diversity-oriented synthetic modifications and the construction of vital molecules of therapeutic interest. This journal is © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Royal Society of Chemistry | en_US |
dc.source | New Journal of Chemistry | en_US |
dc.subject | Aldehydes | en_US |
dc.subject | Benzyl alcohol | en_US |
dc.subject | Dehydrogenative coupling | en_US |
dc.subject | Directing groups | en_US |
dc.subject | Oxidative conditions | en_US |
dc.subject | Palladium-catalyzed | en_US |
dc.subject | Regio-selective | en_US |
dc.subject | Regioselective coupling | en_US |
dc.subject | Synthetic modifications | en_US |
dc.subject | Regioselectivity | en_US |
dc.subject | 2 arylquinazolinone | en_US |
dc.subject | aldehyde | en_US |
dc.subject | benzyl alcohol derivative | en_US |
dc.subject | carbon | en_US |
dc.subject | hydrogen | en_US |
dc.subject | hydroxyl group | en_US |
dc.subject | natural product | en_US |
dc.subject | oxidizing agent | en_US |
dc.subject | palladium | en_US |
dc.subject | quinazolinone derivative | en_US |
dc.subject | unclassified drug | en_US |
dc.subject | Article | en_US |
dc.subject | atom | en_US |
dc.subject | catalysis | en_US |
dc.subject | catalyst | en_US |
dc.subject | chemical bond | en_US |
dc.subject | controlled study | en_US |
dc.subject | electron | en_US |
dc.subject | oxidation | en_US |
dc.subject | oxidative coupling | en_US |
dc.subject | priority journal | en_US |
dc.subject | substitution reaction | en_US |
dc.title | The regioselective coupling of 2-arylquinazolinone C-H with aldehydes and benzyl alcohols under oxidative conditions | en_US |
dc.type | Journal Article | en_US |
Appears in Collections: | Department of Chemistry |
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