Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2059
Title: Organocatalytic γ′[C(sp3)–H] Functionalization of Ynones: An Unusual Approach for the Cyclopentannulation of Benzothiophenes
Authors: Grover, J.
Raghu, M.
Hazra, R.
Mondal, A.
Ramasastry, S.S.V.
Keywords: Organophosphines
Hydroalkylation
Cyclopentannulation
Ynones
Benzothiophenes
Issue Date: 2018
Publisher: Georg Thieme Verlag
Citation: Synthesis (Germany), 50(7), pp. 1462-1470
Abstract: An efficient organocatalytic approach for the cyclopenta[b]annulation of benzothiophenes via γ′[C(sp3)–H] functionalization of ynones is described. Nucleophilic addition of an organophosphine to the designed ynones generates heteroaryl-based ortho-quinodimethanes (oQDMs), which undergo carbocyclization to provide a variety of cyclopenta-fused benzothiophenes. This approach also constitutes an unusual organophosphine-catalyzed intramolecular hydroalkylation of ynones.
URI: https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0036-1591526
http://hdl.handle.net/123456789/2059
Appears in Collections:Research Articles

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