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Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/610
Title: Phosphine-mediated reaction of 3-alkyl allenoates and diaryl 1,2-diones: efficient diastereoselective synthesis of fully substituted cyclopentenones
Authors: Anu Jose
Seetha Lakshmi, K C
Suresh, E
Vijay Nair, G
Keywords: Bond-forming reactions
Dimethyl acetylenedicarboxylate
Multicomponent reactions
Diethyl azodicarboxylate
Heterocyclic compounds
Tert-butylisonitrile
Catalyzed synthesis
Controlled adduct
Ternary compounds
Facile synthesis
Issue Date: 2013
Publisher: American Chemical Society
Citation: Organic Letters 15(8):1858-1861;2013
Abstract: An efficient phosphine-mediated diastereoselective synthesis of substituted cyclopentenones from 3-alkyl allenoates and diaryl 1,2-diones is described.
URI: http://hdl.handle.net/123456789/610
Appears in Collections:2013

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