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73 auth. W. Alvey, F. Scheuren, Alvey, Wendy, G. Wagner, Newcombe, D. Flaherty, Edward H. Hanis, Mitchell, Us, Tiné, S. Livingstone, Aziz, Faye, Qualit Yof, ... Mortalitv Redortino, In Ssa, M. G. Arellano, R. Coulter, Faye Buckler, Warren, F. Aziz, B. Kilss, J. Baldwin, E. Acheson, Donald, Rachel. Brown, D. Childers, Pogan, Howard Matching, I. Records, P. Clark, Service, Richard W Mergerson, J. W., L. Cox, Bruce Johnson, Sarah-K. McDonald, D. Nelson, Vazquez, Janet Crane, Douglas K1eweno, G. Duncan, Lambert, Diane, Nancy H. Fink, Fdwarrl H Hanis, S. P. Ancl Mitchell, G. Howe, D. Fraser, Lindsay, Gen, G. How, J. Lindsay, E. Coppock, A. Miller, W. Butz, J. Carroll, J. Norwood, Charles Waite, Johnson, David Liss, T. L, Witt, N. Johnson, C. Glover, Rogot, J. Kagawa, Mi, Martln Llavl, A. Katz, Klaus Teuter, P. Sidel
As a consequence of the importance of nitrogen-containing compounds in biological and pharmaceutical applications, methods for the construction of carbon-nitrogen bonds have been heavily studied for at least 150 years. Hydroamination, the addition o…
As a consequence of the importance of nitrogen-containing compounds in biological and pharmaceutical applications, methods for the construction of carbon-nitrogen bonds have been heavily studied for at least 150 years. Hydroamination, the addition of HNR2 across a carbon-carbon π bond, is in principle one of the most atom-economical methods for the synthesis of this class of compounds. Catalytic hydroaminations of alkenes, allenes, and dienes (which may be interor intramolecular) afford amines, imines, and enamines (Eq. 1).
1
 5 2000