Molecules 2000, 5(11), 1182-1186; doi:10.3390/51101182
Article

The Reaction of Trimethylsilylethynyl(phenyl)iodonium Triflate with Some Phenolates: Formation of Substitution and sp2 C-H Insertion Products

, * email and
Received: 22 August 2000; in revised form: 5 October 2000 / Accepted: 10 October 2000 / Published: 1 November 2000
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: Treatment of trimethylsilylethynyl(phenyl)iodonium triflate with the potassium salts of some acidic phenols results in the formation of substitution products (O-trimethylsilylethynylphenols and/or O-ethynylphenols), along with sp2C-H insertion products which afford eventually 2-aroxybenzo[b]furans.
Keywords: Alkynyl iodonium salts; ethynyl phenyl ethers; benzo[b]furans
PDF Full-text Download PDF Full-Text [29 KB, uploaded 18 June 2014 19:25 CEST]

Export to BibTeX |
EndNote


MDPI and ACS Style

Nikas, S.; Rodios, N.; Varvoglis, A. The Reaction of Trimethylsilylethynyl(phenyl)iodonium Triflate with Some Phenolates: Formation of Substitution and sp2 C-H Insertion Products. Molecules 2000, 5, 1182-1186.

AMA Style

Nikas S, Rodios N, Varvoglis A. The Reaction of Trimethylsilylethynyl(phenyl)iodonium Triflate with Some Phenolates: Formation of Substitution and sp2 C-H Insertion Products. Molecules. 2000; 5(11):1182-1186.

Chicago/Turabian Style

Nikas, Spyros; Rodios, Nestor; Varvoglis, Anastasios. 2000. "The Reaction of Trimethylsilylethynyl(phenyl)iodonium Triflate with Some Phenolates: Formation of Substitution and sp2 C-H Insertion Products." Molecules 5, no. 11: 1182-1186.


Molecules EISSN 1420-3049 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert