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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