Nickel-catalyzed amination of aryl sulfamates
- PMID: 21344578
- PMCID: PMC3389547
- DOI: 10.1002/anie.201007325
Nickel-catalyzed amination of aryl sulfamates
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Wolfe JP, Wagaw S, Marcoux J-F, Buchwald SL. Acc. Chem. Res. 1998;31:805–818. Hartwig JF. Angew. Chem. 1998;110:2154–2177. Angew. Chem. Int. Ed. 1998;37:2046–2067. c) “Practical Palladium Catalysts for C–N and C–O Bond Formation”: Muci AR, Buchwald SL. In: Topics in Current Chemistry. Miyaura N, editor. Vol. 219. Berlin: Springer; 2001. p. 131. Kienle M, Dubbaka SR, Brade K, Knochel P. Eur. J. Org. Chem. 2007:4166–4176.
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The amination of aryl methyl ethers proceeds most efficiently using 2-methoxynaphthalene and cyclic secondary amines; see: Shimasaki T, Chatani N. Chem. Lett. 2009;38:710–711.
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