Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9082
Full metadata record
DC FieldValueLanguage
dc.contributor.authorGuin, Soumitraen_US
dc.contributor.authorSamanta, Sampaken_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:30:58Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:30:58Z-
dc.date.issued2018-
dc.identifier.citationDagar, 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.201700511en_US
dc.identifier.issn2193-5807-
dc.identifier.otherEID(2-s2.0-85034242699)-
dc.identifier.urihttps://doi.org/10.1002/ajoc.201700511-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9082-
dc.description.abstractA 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, Weinheimen_US
dc.language.isoenen_US
dc.publisherWiley-VCH Verlagen_US
dc.sourceAsian Journal of Organic Chemistryen_US
dc.titleAgSbF6-Catalyzed Tandem Reaction of 2-Alkynylanilines with Cyclic Enynones: Efficient access to 3-Furo[3,2-c]chromenylindoles and Related Scaffoldsen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Altmetric Badge: