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1
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-
84944041959
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-
For reviews see:. Katritzky A.R., Rees C.W., and Scriven E.F.V. (Eds), Pergamon Press, Oxford
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For reviews see:. Neunhoeffer H. In: Katritzky A.R., Rees C.W., and Scriven E.F.V. (Eds). Comprehensive Heterocyclic Chemistry II Vol. 6 (1996), Pergamon Press, Oxford 507-573
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(1996)
Comprehensive Heterocyclic Chemistry II
, vol.6
, pp. 507-573
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Neunhoeffer, H.1
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2
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33646136917
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-
Weinreb S.M. (Ed), Thieme, Stuttgart
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Lindsley C.W., and Layton M.E. In: Weinreb S.M. (Ed). Science of Synthesis Vol. 17 (2003), Thieme, Stuttgart 357-447
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(2003)
Science of Synthesis
, vol.17
, pp. 357-447
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-
Lindsley, C.W.1
Layton, M.E.2
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3
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10644249108
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-
For recent examples see:
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For recent examples see:. Alphonse F.-A., Suzenet F., Keromnes A., Lebret B., and Guillaumet G. Synthesis (2004) 2893-2899
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(2004)
Synthesis
, pp. 2893-2899
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Alphonse, F.-A.1
Suzenet, F.2
Keromnes, A.3
Lebret, B.4
Guillaumet, G.5
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4
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0037415505
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Zhao Z., Leister W.H., Strauus K.A., Wisnowski D.D., and Lindsley C.W. Tetrahedron Lett. 44 (2003) 1123-1127
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(2003)
Tetrahedron Lett.
, vol.44
, pp. 1123-1127
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-
Zhao, Z.1
Leister, W.H.2
Strauus, K.A.3
Wisnowski, D.D.4
Lindsley, C.W.5
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5
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33646155750
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-
see also Refs. 2-5.
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-
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7
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2442417566
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Wang X.-L., Chao H., Li H., Hong X.-L., Liu Y.-J., Tan L.-F., and Ji L.-N. Inorg. Biochem. 98 (2004) 1143-1150
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(2004)
Inorg. Biochem.
, vol.98
, pp. 1143-1150
-
-
Wang, X.-L.1
Chao, H.2
Li, H.3
Hong, X.-L.4
Liu, Y.-J.5
Tan, L.-F.6
Ji, L.-N.7
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8
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0142143114
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Hudson M.J., Drew M.G.B., Foreman M.R.StJ., Hill C., Huet N., Madie C., and Youngs T.G.A. Dalton Trans. (2003) 1675-1685
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(2003)
Dalton Trans.
, pp. 1675-1685
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-
Hudson, M.J.1
Drew, M.G.B.2
Foreman, M.R.StJ.3
Hill, C.4
Huet, N.5
Madie, C.6
Youngs, T.G.A.7
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11
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0003719612
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For reviews covering the cycloaddition reactions of heterocyclic azadienes see:, Academic Press, London Chapter 10, pp 300-358
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For reviews covering the cycloaddition reactions of heterocyclic azadienes see:. Boger D.L., and Weinreb S.N. Hetero Diels-Alder Methodology in Organic Synthesis (1987), Academic Press, London Chapter 10, pp 300-358
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(1987)
Hetero Diels-Alder Methodology in Organic Synthesis
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Boger, D.L.1
Weinreb, S.N.2
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14
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0022398192
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and references cited therein
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Boger D.L., and Panek J.S. J. Am. Chem. Soc. 107 (1985) 5745-5754 and references cited therein
-
(1985)
J. Am. Chem. Soc.
, vol.107
, pp. 5745-5754
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-
Boger, D.L.1
Panek, J.S.2
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15
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13444262334
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For recent examples see:
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For recent examples see:. Kozhevnikov V.N., Kozhevnikov D.N., Shabunina O.V., Rusinov V.L., and Chupakhin O.N. Tetrahedron Lett. 46 (2005) 1521-1523
-
(2005)
Tetrahedron Lett.
, vol.46
, pp. 1521-1523
-
-
Kozhevnikov, V.N.1
Kozhevnikov, D.N.2
Shabunina, O.V.3
Rusinov, V.L.4
Chupakhin, O.N.5
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16
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13944258152
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Kozhevnikov V.N., Kozhevnikov D.N., Shabunina O.V., Rusinov V.L., and Chupakhin O.N. Tetrahedron Lett. 46 (2005) 1791
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(2005)
Tetrahedron Lett.
, vol.46
, pp. 1791
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-
Kozhevnikov, V.N.1
Kozhevnikov, D.N.2
Shabunina, O.V.3
Rusinov, V.L.4
Chupakhin, O.N.5
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24
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28844466070
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For a review, see:
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For a review, see:. Taylor R.J.K., Reid M., Foot J., and Raw S.A. Acc. Chem. Res. 38 (2005) 851-869
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(2005)
Acc. Chem. Res.
, vol.38
, pp. 851-869
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-
Taylor, R.J.K.1
Reid, M.2
Foot, J.3
Raw, S.A.4
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26
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0026785118
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Non-commercial α-hydroxyketones were prepared from the corresponding methyl ketones using a published procedure:
-
Non-commercial α-hydroxyketones were prepared from the corresponding methyl ketones using a published procedure:. Moriarty R.M., Berglund B.A., and Penmasta R. Tetrahedron Lett. 33 (1992) 6065-6068
-
(1992)
Tetrahedron Lett.
, vol.33
, pp. 6065-6068
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-
Moriarty, R.M.1
Berglund, B.A.2
Penmasta, R.3
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27
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33646123566
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note
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1H NMR data.
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-
-
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29
-
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33646163944
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-
note
-
+, 241.1446 (3.5 ppm error)].
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-
-
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30
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33646162217
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note
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Microwaves could also be employed for the second step (PhMe, 120 °C, 1 h), although the initial condensation proceeded more efficiently under thermal conditions.
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-
-
-
31
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33646151190
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note
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+, 273.1393 (-0.6 ppm error)].
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