A general and efficient method for the Suzuki-Miyaura coupling of 2-pyridyl nucleophiles
- PMID: 18491343
- PMCID: PMC2748766
- DOI: 10.1002/anie.200801465
A general and efficient method for the Suzuki-Miyaura coupling of 2-pyridyl nucleophiles
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References
-
-
Recent Reviews: Miyaura N. Top. Curr. Chem. 2002;219:11–59. Bellina F, Carpita A, Rossi R. Synthesis. 2004;15:2419. Miyaura N. In: Metal-Catalyzed Cross-Coupling Reaction. Diederich F, de Meijere A, editors. Wiley-VCH; New York: 2004. Chapter 2.
-
-
- Barder TE, Walker SD, Martinelli JR, Buchwald SL. J. Am. Chem. Soc. 2005;127:4685–4696. - PubMed
-
-
For a review of the Suzuki-Miyaura reaction of heteroaryl nucleophiles, see: Tyrell E, Brookes P. Synthesis. 2004;4:469–483.
-
-
- Billingsley KL, Buchwald SL. J. Am. Chem. Soc. 2007;129:3358–3366. - PubMed
-
- Richardson CM, Gillespie RJ, Williamson DS, Jordan AM, Fink A, Knight AR, Sellwood DM, Misra A. Bioorg. Med. Chem. Lett. 2006;16:5993–5997. - PubMed
- Gellibert F, De Gouville A-C, Woolven J, Mathews N, Nguyen V-L, Bertho-Ruault C, Patikis A, Grygielko ET, Laping NJ, Huet S. J. Med. Chem. 2006;49:2210–2221. - PubMed
- Salama I, Hocke C, Utz W, Prante O, Boeckler F, Huebner H, Kuwert T, Gmeiner P. J. Med. Chem. 2007;50:489–500. - PubMed
- Meyers KM, Kim N, Mendez-Andino JL, Hu XE, Mumin RN, Klopfenstein SR, Wos JA, Mitchell MC, Paris JL, Ackley DC, Holbert JK, Mittelstadt SW, Reizes O. Bioorg. Med. Chem. Lett. 2007;17:814–818. - PubMed
- Anderson DR, Meyers MJ, Vernier WF, Mahoney MW, Kurumbail RG, Caspers N, Poda GI, Schindler JF, Reitz DB, Mourey RJ. J. Med. Chem. 2007;50:2647–2654. - PubMed
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