A novel and efficient oxidative biaryl coupling reaction of phenol ether derivatives using a combination of hypervalent iodine(iii) reagent and heteropoly acid
β Scribed by Hamamoto, Hiromi; Anilkumar, Gopinathan; Tohma, Hirofumi; Kita, Yasuyuki
- Book ID
- 118242504
- Publisher
- Royal Society of Chemistry
- Year
- 2002
- Tongue
- English
- Weight
- 133 KB
- Volume
- 5
- Category
- Article
- ISSN
- 1359-7345
- DOI
- 10.1039/b111178g
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
First facile and efficient oxidative coupling reaction of alkylarenes leading to alkylbiaryls using a combination of hypervalent iodine(III) reagent, phenyliodine(III) bis(trifluoroacetate) (PIFA), and BF 3 β’Et 2 O has been developed.
The oxidative intramolecular coupling reaction of phenol ether derivatives (nonphenolic derivatives) on treatment with a novel combination of a hypervalent iodine(III) reagent, phenyliodine bis(trifluoroacetate) (PIFA), and heteropoly acid (HPA) was studied. Biaryl compounds were obtained in excelle