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Publikováno v:
Wilting, J, Janssen, M H M, Muller, C J & Vogt, D 2006, ' The enantioselective step in the nickel-catalyzed hydrocyanation of 1,3-cyclohexadiene ', Journal of the American Chemical Society, vol. 128, no. 35, pp. 11374-5 . https://doi.org/10.1021/ja064378u
Journal of the American Chemical Society, 128(35), 11374-11375. American Chemical Society
Journal of the American Chemical Society, 128(35), 11374-5. American Chemical Society
Journal of the American Chemical Society, 128(35), 11374-11375. American Chemical Society
Journal of the American Chemical Society, 128(35), 11374-5. American Chemical Society
On the basis of deuterium labeling experiments and an equal 1,2-/1,4-product distribution, the reductive elimination of the product has been established to be the enantioselective step in the nickel-catalyzed hydrocyanation of 1,3-cyclohexadiene. Thi
Publikováno v:
Journal of the American Chemical Society. 128(25)
Nickel complexes having a bulky tri(sec-alkyl)phosphine ligand catalyze hydroheteroarylation of alkynes at 35 degrees C. Selective activation of an Ar-H bond over an Ar-CN bond of N-protected 3-cyanoindoles is achieved by a proper choice of ligand an