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1
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0038359011
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DRL Publication No. 284
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DRL Publication No. 284.
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2
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0038359012
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Trost, B. M.; Flemming, I., Eds.; Pergamon: Oxford; and references therein
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Jung, M. E. In Comprehensive Organic Synthesis, Vol. 4; Trost, B. M.; Flemming, I., Eds.; Pergamon: Oxford, 1991, 30-39; and references therein.
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(1991)
Comprehensive Organic Synthesis
, vol.4
, pp. 30-39
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Jung, M.E.1
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3
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0037129388
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(a) Kobayashi, S.; Kakamuto, K.; Sugiura, M. Org. Lett. 2002, 4, 1319.
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(2002)
Org. Lett.
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Kobayashi, S.1
Kakamuto, K.2
Sugiura, M.3
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4
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0035953052
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(b) Kolarovic, A.; Berkeš, D.; Baran, P.; Povazanec, F. Tetrahedron Lett. 2001, 42, 2579.
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(2001)
Tetrahedron Lett.
, vol.42
, pp. 2579
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Kolarovic, A.1
Berkeš, D.2
Baran, P.3
Povazanec, F.4
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5
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0035935120
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(c) Shaikh, N. S.; Deshpande, V. H.; Bedekar, A. V. Tetrahedron 2001, 57, 9045.
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(2001)
Tetrahedron
, vol.57
, pp. 9045
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Shaikh, N.S.1
Deshpande, V.H.2
Bedekar, A.V.3
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6
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0035966174
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(d) Bartoli, G.; Bosco, M.; Marcantoni, E.; Petrini, M.; Sambri, L.; Torregiani, E. J. Org. Chem. 2001, 66, 9052.
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(2001)
J. Org. Chem.
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Bartoli, G.1
Bosco, M.2
Marcantoni, E.3
Petrini, M.4
Sambri, L.5
Torregiani, E.6
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7
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0037078429
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Grimaud, L.; Rotulo, D.; Ros-Perez, R.; Guitry-Azam, L.; Prunet, J. Tetrahedron Lett. 2002, 43, 7477.
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(2002)
Tetrahedron Lett.
, vol.43
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Grimaud, L.1
Rotulo, D.2
Ros-Perez, R.3
Guitry-Azam, L.4
Prunet, J.5
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8
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0037078387
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(a) Kamimura, A.; Murakami, N.; Yokota, K.; Shirai, M.; Okamoto, H. Tetrahedron Lett. 2002, 43, 7521.
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(2002)
Tetrahedron Lett.
, vol.43
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Kamimura, A.1
Murakami, N.2
Yokota, K.3
Shirai, M.4
Okamoto, H.5
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9
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0035973773
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(b) Skarżewski, J.; Zielińska-Błajet, M.; Turowska-Tyrk, I. Tetrahedron: Asymmetry, 2001, 12, 1923.
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(2001)
Tetrahedron: Asymmetry
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Skarzewski, J.1
Zielińska-Błajet, M.2
Turowska-Tyrk, I.3
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10
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0037131766
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(c) Nishide, K.; Miyamoto, T.; Kumar, K.; Ohsugu, S.; Node, M. Tetrahedron Lett. 2002, 43, 8569.
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(2002)
Tetrahedron Lett.
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Nishide, K.1
Miyamoto, T.2
Kumar, K.3
Ohsugu, S.4
Node, M.5
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11
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0037010780
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(d) Abrouki, Y.; Zahouily, M.; Rayadh, A.; Bahlaouan, B.; Sebti, S. Tetrahedron Lett. 2002, 43, 8951.
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(2002)
Tetrahedron Lett.
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Abrouki, Y.1
Zahouily, M.2
Rayadh, A.3
Bahlaouan, B.4
Sebti, S.5
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12
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0037131734
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Keglevich, G.; Sipos, M.; Imre, T.; Ludányi, K.; Szieberth, D.; Töke, L. Tetrahedron Lett. 2002, 43, 8515.
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(2002)
Tetrahedron Lett.
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Keglevich, G.1
Sipos, M.2
Imre, T.3
Ludányi, K.4
Szieberth, D.5
Töke, L.6
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15
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0025305393
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and references cited herein (for anti-inflammatory study). In this report, twenty different aldoximes and ketoximes were added to ethyl acrylate using KOH (16 mol%) as base catalyst in EtOH solvent
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As an example, see: Macchia, B.; Balsamo, A.; Lapucci, A.; Macchia, F.; Martinelli, A.; Nencetti, S.; Orlandini, E.; Baldacci, M.; Mengozzi, G.; Soldani, G.; Domiano, P. J. Med. Chem. 1990, 33, 1423; and references cited herein (for anti-inflammatory study). In this report, twenty different aldoximes and ketoximes were added to ethyl acrylate using KOH (16 mol%) as base catalyst in EtOH solvent.
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(1990)
J. Med. Chem.
, vol.33
, pp. 1423
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Macchia, B.1
Balsamo, A.2
Lapucci, A.3
Macchia, F.4
Martinelli, A.5
Nencetti, S.6
Orlandini, E.7
Baldacci, M.8
Mengozzi, G.9
Soldani, G.10
Domiano, P.11
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16
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0036691909
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For recent medicinal chemistry on oxime based compounds, see: Takamura, M.; Yanagisawa, H.; Kanai, M.; Shibasaki, M. Chem. Pharm. Bull. 2002, 50, 1118.
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(2002)
Chem. Pharm. Bull.
, vol.50
, pp. 1118
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Takamura, M.1
Yanagisawa, H.2
Kanai, M.3
Shibasaki, M.4
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17
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0029796652
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and references cited therein
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Triphenylphosphine is known as a catalyst for the Michael addition of carbon nucleophiles. Please see: Gómez-Bengoa, E.; Cuerva, J. M.; Mateo, C.; Echavarren, A. M. J. Am. Chem. Soc. 1996, 118, 8553; and references cited therein.
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(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 8553
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Gómez-Bengoa, E.1
Cuerva, J.M.2
Mateo, C.3
Echavarren, A.M.4
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18
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0034966613
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For a recent report on triphenylphosphine catalyzed Michael addition of carbon nucleophiles, see: Lumbierres, M.; Marchi, C.; Moreno-Mañas, M.; Sebastian, R. M.; Vallribera, A.; Lago, E.; Molins, E. Eur. J. Org. Chem. 2001, 2321.
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(2001)
Eur. J. Org. Chem.
, pp. 2321
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Lumbierres, M.1
Marchi, C.2
Moreno-Mañas, M.3
Sebastian, R.M.4
Vallribera, A.5
Lago, E.6
Molins, E.7
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19
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0038697216
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note
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Oximes were prepared by reacting the corresponding carbonyl compounds with excess of hydroxylamine in methanol, either at r.t. or when required under heating (55°c).
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