Abstract
The author's extensive studies aimed at elaboration of synthetic strategies, and investigation of structure, reactivity pattern, and biological activity of new classes of organic compounds, viz., alkynyloiodonium salts and ynol esters, are reviewed.
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E.De Clercq, D.R.Fischer, and P.J.Stang, to be published.
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Based upon a lecture given at the Institute of Organic Chemistry, Moscow, on February 25, 1992, on the occasion of the award of a D.Sc. (honoris causa) and upon two recent related reviews1,2 on the same topics.
Translated fromIzvestiya Akademii Nauk, Seriya Khimicheskaya, No. 1, pp. 20–31, January, 1993.
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Stang, P.J. Ynol esters and alkynyl(phenyl)iodonium chemistry. Russ Chem Bull 42, 12–23 (1993). https://doi.org/10.1007/BF00699967
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DOI: https://doi.org/10.1007/BF00699967
Key words
- alkynyl(aryl)iodonium salts preparation and structure
- bis(iodonium)acetylenes and diacetylenes
- nucleophilic acetylenic substitution
- “alkynylation” using iodonium salts of dienophiles ynol esters preparation and structure
- hydrolysis and generation of ynolates
- ynol esters as dienophiles
- inhibitor activity with respect to proteases and phosphatases