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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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