Palladium-catalyzed cross coupling of Grignard reagents with in situ-derived enol phosphates

Author:

Miller Joseph A.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference4 articles.

1. Cross coupling of vinyl triflates and alkyl Grignard reagents catalyzed by nickel(0)-complexes

2. Synthetic Transformations of Vinyl and Aryl Triflates

3. See the following representative references for Ni- or Pd-catalyzed cross coupling of enol phosphates with organometallic reagents: (a) Pd/R3Al: Takai, K.; Sato, M.; Oshima, K.; Nozaki, H. Bull. Chem. Soc. Jpn. 1984, 57, 108; (b) Ni/R3Al: Fukamiya, N.; Oki, M.; Aratani, T. Chem. Ind. (London) 1981, 606; (c) Ni- or Pd/Me3SiCH2MgCl: Hayashi, T.; Fujiwa, T.; Okamoto, Y.; Katsuro, Y.; Kumada, M. Synthesis 1981, 1001; (d) Ni/RMgX: Sofia, A.; Karlstrom, E.; Itami, K.; Backvall, J. J. Org. Chem. 1999, 64, 1745; (e) Ni/RZnX: Wu, J.; Yang, Z. J. Org. Chem. 2001, 66, 7875; (f) Pd/RnMn: Fugami, K.; Oshima, K.; Utimoto, K. Chem. Lett. 1987, 2203.

4. New Plumbylenes and a Plumbylene Dimer with a Short Lead−Lead Separation,1

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