Heterocycles via cyclization of alkynes promoted by organopalladium complexes

Author:

Cacchi Sandro

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference68 articles.

1. The palladium-catalyzed reaction of aryl iodides with mono and disubstituted acetylenes: a new synthesis of trisubstituted alkenes.

2. For other examples of palladium-catalyzed overall trans additions to acetylenic compounds, see D. Zargarian, H. Alper, Organometallics 10 (1991) 2914. G. Dyker, A. Kellner, Tetrahedron Lett. 35 (1994) 7633. P. de Vaal, A. Dedieu, J. Organomet. Chem. 478 (1994) 121. R.A. Gibbs, U. Krishnan, J.M. Dolence, C.D. Poulter, J. Org. Chem. 60 (1995) 7821. J. Ji, Z. Wang, X. Lu, Organometallics 15 (1996) 2821.

3. Vinylidene transition-metal complexes. 18. (Arene)osmium complexes containing alkynyl, vinyl, vinylidene, and thio- and selenoketene units as ligands: a series of organometallic compounds built up from 1-alkynes

4. Mechanism, regiochemistry, and stereochemistry of the insertion reaction of alkynes with methyl(2,4-pentanedionato)(triphenylphosphine)nickel. A cis insertion that leads to trans kinetic products

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