Palladium-Catalyzed Reaction of o-Ethynylphenols, o-((Trimethylsilyl)ethynyl)phenyl Acetates, and o-Alkynylphenols with Unsaturated Triflates or Halides: A Route to 2-Substituted-, 2,3-Disubstituted-, and 2-Substituted-3-acylbenzo[b]furans
Author:
Affiliation:
1. Dipartimento di Chimica, Ing. Chimica e Materiali, Via Vetoio, 67100 L'Aquila, Italy, and Dipartimento di Studi di Chimica e Tecnologia delle Sostanze Biologicamente Attive, Università “La Sapienza”, P.le A. Moro 5, I-00185 Roma, Italy
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo961051a
Reference30 articles.
1. The palladium-tributylammonium formate reagent in the stereoselective hydrogenation, and stereo- and regioselective hydroarylation of alkyl 4-hydroxy-2-alkynoates: a route to substituted butenolides
2. Palladium-Catalyzed Reaction of 2-Hydroxyaryl and Hydroxyheteroaryl Halides with 1-Alkynes: An Improved Route to the Benzo[b]furan Ring System
3. Palladium-catalysed coupling of aryl and vinyl triflates or halides with 2-ethynylaniline: An efficient route to functionalized 2-substituted indoles
4. Propargyl Ethylmalonates as Useful Building Blocks for the Preparation of Functionalized Butenolides
5. Palladium-catalysed cyclization of 2-alkynylanilines to 2-substituted indoles under an acidic two-phase system
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