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1
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0003594801
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Recent reviews on electrophilic amination:, VCH Publishers: Weinheim
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Recent reviews on electrophilic amination: Mulzer, J.; Altenbach, H.-J.; Braun, M.; Krohn, K.; Reissig, H.-U. Organic Synthesis Highlights; VCH Publishers: Weinheim, 1991; pp 45–53.
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Mulzer, J.1
Altenbach, H.-J.2
Braun, M.3
Krohn, K.4
Reissig, H.-U.5
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3
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0001670922
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See also
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See also: Oppolzer, W.; Tamura, O.; Sundarababu, G.; Signer, M. J. Am. Chem. Soc. 1992, 114, 5900–5902.
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J. Am. Chem. Soc.
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Oppolzer, W.1
Tamura, O.2
Sundarababu, G.3
Signer, M.4
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4
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Genêt, J.-P.; Mallart, S.; Greck, C.; Piveteau, E. Tetrahedron Lett. 1991, 32, 2359–2362.
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Tetrahedron Lett.
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Genêt, J.-P.1
Mallart, S.2
Greck, C.3
Piveteau, E.4
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6
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37049090651
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Vidal, J.; Drouin, J.; Collet, A. J. Chem. Soc., Chem. Commun. 1991, 435–437.
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Vidal, J.1
Drouin, J.2
Collet, A.3
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7
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0000702355
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Enders, D.; Fey, P.; Kipphardt, H. Org. Synth. 1987, 65, 173–182.
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Org. Synth.
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Enders, D.1
Fey, P.2
Kipphardt, H.3
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8
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0001541620
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Enders, D.; Kipphardt, H.; Fey, P. Org. Synth. 1987, 65, 183–301.
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Org. Synth.
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Enders, D.1
Kipphardt, H.2
Fey, P.3
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9
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0000857662
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We used BocF instead of BocCl, in view of the known instability of the latter. For the preparation of BocF, see
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We used BocF instead of BocCl, in view of the known instability of the latter. For the preparation of BocF, see: Dang, V. A.; Olofson, R. A.; Wolf, P. R.; Piteau, M. D.; Senet, J.-P.G. J. Org. Chem. 1990, 55, 1847–1851.
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Dang, V.A.1
Olofson, R.A.2
Wolf, P.R.3
Piteau, M.D.4
Senet, J.-P.G.5
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11
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0001278278
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The photochemical, thermal, or acid-catalyzed rearrangement of oxaziridines to amides is a well-documented reaction; for examples of photochemical isomerizations see
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The photochemical, thermal, or acid-catalyzed rearrangement of oxaziridines to amides is a well-documented reaction; for examples of photochemical isomerizations see: Oliveros, E.; Rivière, M.; Lattes, A. Nouv. J. Chim. 1979, 3, 739–753.
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Nouv. J. Chim.
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Oliveros, E.1
Rivière, M.2
Lattes, A.3
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12
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0001091341
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Aubé, J.; Hammond, M.; Gherardini, E.; Takusagawa, F. J. Org. Chem. 1991, 56, 499–508.
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Aubé, J.1
Hammond, M.2
Gherardini, E.3
Takusagawa, F.4
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13
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0000080874
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Examples of thermal or acid-catalyzed rearrangements
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Examples of thermal or acid-catalyzed rearrangements: Lattes, A.; Oliveros, E.; Rivière, M.; Belzecki, C.; Mostowicz, D.; Abramskj, W.; Piccini-Leopardi, C.; Germain, G.; Van Meerssche, M. J. Am. Chem. Soc. 1982, 104, 3929–3934.
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Lattes, A.1
Oliveros, E.2
Rivière, M.3
Belzecki, C.4
Mostowicz, D.5
Abramskj, W.6
Piccini-Leopardi, C.7
Germain, G.8
Van Meerssche, M.9
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14
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28744454673
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We have no evidence, however, that such a rearrangement may occur during the preparation 2b, and we suspect that the formation of 7 is actually due to a side reaction rather than to the isomerization of 2b
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Plaquevent, J.-C.; Bénard, D.; Goument, B. New. J. Chem. 1991, 15, 579–585. We have no evidence, however, that such a rearrangement may occur during the preparation 2b, and we suspect that the formation of 7 is actually due to a side reaction rather than to the isomerization of 2b.
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Bénard, D.2
Goument, B.3
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Hydrazinopeptides are currently the object of many chemical and biological studies. See
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Hydrazinopeptides are currently the object of many chemical and biological studies. See: Viret, J.; Gabard, J.; Collet, A. Tetrahedron 1987, 43, 891–894.
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Tetrahedron
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Gabard, J.2
Collet, A.3
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Amour, A.; Collet, A.; Dubar, C.; Reboud, M. Submitted
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Aubry, A.; Bayeul, D.; Mangeot, J.-P.; Vidal, J.; Sterin, S.; Collet, A.; Lecoq, A.; Marraud, M. Biopolymers 1991, 32, 793–801. Amour, A.; Collet, A.; Dubar, C.; Reboud, M. Submitted.
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Bayeul, D.2
Mangeot, J.-P.3
Vidal, J.4
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Collet, A.6
Lecoq, A.7
Marraud, M.8
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Berrang, B. D.; Lewin, A. H.; Carroll, F. I. J. Org. Chem. 1982, 47, 2643–2647.
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Decorte, E.; Caplar, V.; Sega, A.; Sunjic, V. Acta Pharm. Jugoslav. 1980, 30, 183–187.
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