Addition of 1,3-dicarbonyl compounds to terminal alkynes catalyzed by a cationic cobalt(iii) complex
Author:
Affiliation:
1. Department of Chemistry
2. Indian Institute of Technology Kharagpur
3. Kharagpur 721302
4. India
Abstract
The Nakamura reaction using the complex, [Cp*Co(CH3CN)3][SbF6]2 as the catalyst has been described. Alkynes on reaction with β-ketoesters afford tetrasubstituted benzenes.
Funder
Science and Engineering Research Board
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2020/RA/D0RA05923D
Reference22 articles.
1. Atom Economy—A Challenge for Organic Synthesis: Homogeneous Catalysis Leads the Way
2. Transition-Metal-Catalyzed C–H Alkylation Using Alkenes
3. Indium-Catalyzed Addition of Active Methylene Compounds to 1-Alkynes
4. Indium-Catalyzed 2-Alkenylation of 1,3-Dicarbonyl Compounds with Unactivated Alkynes
5. Construction of a Chiral Quaternary Carbon Center by Indium-Catalyzed Asymmetric α-Alkenylation of β-Ketoesters
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1. Regio- and Stereoselective Intermolecular Oxysulfonylation of Alkynes with 1,3-Diketones to Access (Z)-β-Sulfonated Enethers;The Journal of Organic Chemistry;2023-09-22
2. Synthesis of 4-aryl-3,4-dihydrocoumarins and 4-aryl-4H-chromenes via Er(OTf)3-catalyzed cascade reactions of p-quinone methides with 1,3-dicarbonyl compounds;RSC Advances;2023
3. DBU- and DABCO-Promoted Selective Access to 2,5-Diarylnitrobenzoates and Cyclohexenones via One-Pot Reactions;Synlett;2022-04-05
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