Double Insertion of Coordinated Phosphanylalkyne Ligands into a Pt−C6F5 Bond
✍ Scribed by Jonathan P. H. Charmant; Juan Forniés; Julio Gómez; Elena Lalinde; M. Teresa Moreno; A. Guy Orpen; Santiago Solano
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 119 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0044-8249
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✦ Synopsis
Carbon ± carbon bond forming reactions promoted by transition metals are among the basic goals of organometallic chemistry and play an important role in the design of efficient and selective processes. [1] The intramolecular coupling of alkyne and related C 2 ligands (alkynyl, vinyl, vinylidene) is particularly interesting because it constitutes an effective method for the synthesis of useful organic products. [2] The facile migratory insertion of CC units into MÀH and MÀC bonds seems to be decisive not only for these reactions but also for many catalytic processes. [1, 2] Usually bonds between a metal and a perfluorocarbon atom are quite inert towards insertion reactions, and there is currently little or no knowledge on the insertion of acetylene fragments into the robust MÀR F bonds. [3] mimetics combining the biological activity of b-lactams and the countless bioactive properties of conformationally restricted oligopeptides.
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