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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Guin, Soumitra | en_US |
dc.contributor.author | Samanta, Sampak | en_US |
dc.date.accessioned | 2022-03-17T01:00:00Z | - |
dc.date.accessioned | 2022-03-21T11:30:58Z | - |
dc.date.available | 2022-03-17T01:00:00Z | - |
dc.date.available | 2022-03-21T11:30:58Z | - |
dc.date.issued | 2018 | - |
dc.identifier.citation | Dagar, A., Guin, S., & Samanta, S. (2018). AgSbF6-catalyzed tandem reaction of 2-alkynylanilines with cyclic enynones: Efficient access to 3-furo[3,2-c]chromenylindoles and related scaffolds. Asian Journal of Organic Chemistry, 7(1), 123-127. doi:10.1002/ajoc.201700511 | en_US |
dc.identifier.issn | 2193-5807 | - |
dc.identifier.other | EID(2-s2.0-85034242699) | - |
dc.identifier.uri | https://doi.org/10.1002/ajoc.201700511 | - |
dc.identifier.uri | https://dspace.iiti.ac.in/handle/123456789/9082 | - |
dc.description.abstract | A simple, mild, catalytic and efficient method for the straightforward synthesis of an interesting class of a range of 2-aryl/alkyl-substituted-3-(2-aryl/alkyl-4H-furo[3,2-c]chromen-4-yl)-1H-indoles in good to high yields is reported for the first time. This atom-efficient method proceeds via AgSbF6-catalyzed one-pot sequential intramolecular hydroamination (C−N bond formation) of 2-alkynylanilines followed by Friedel–Crafts alkylation/oxa-cyclization (creation of new C−C and C−O bonds) reaction between in situ generated 2-substituted indoles and several cyclic enynones. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley-VCH Verlag | en_US |
dc.source | Asian Journal of Organic Chemistry | en_US |
dc.title | AgSbF6-Catalyzed Tandem Reaction of 2-Alkynylanilines with Cyclic Enynones: Efficient access to 3-Furo[3,2-c]chromenylindoles and Related Scaffolds | en_US |
dc.type | Journal Article | en_US |
Appears in Collections: | Department of Chemistry |
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