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1
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0011237795
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Synthesis of 4-pyrrolidin-1-yl-5H-furan-2-ones system, see:
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Synthesis of 4-pyrrolidin-1-yl-5H-furan-2-ones system, see: Farina F., Martin M.V., Sanchez F., Maestro M.C., Martin M.R. Synthesis. 1983;397-398.
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(1983)
Synthesis
, pp. 397-398
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Farina, F.1
Martin, M.V.2
Sanchez, F.3
Maestro, M.C.4
Martin, M.R.5
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5
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0026690578
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Schlessinger R.H., Mjalli A.M.M., Adams A.D., Springer J.P., Hoogsteen K. J. Org. Chem. 57:1992;2992-2993.
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(1992)
J. Org. Chem.
, vol.57
, pp. 2992-2993
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Schlessinger, R.H.1
Mjalli, A.M.M.2
Adams, A.D.3
Springer, J.P.4
Hoogsteen, K.5
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7
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0035819447
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Wang J., Jiang X., Chen M., Ge Z., Hu Y., Hu H. J. Chem. Soc., Perkin Trans. 1. 2000;66-71.
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(2000)
J. Chem. Soc., Perkin Trans. 1
, pp. 66-71
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Wang, J.1
Jiang, X.2
Chen, M.3
Ge, Z.4
Hu, Y.5
Hu, H.6
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8
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0027522674
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Transformation of 4-pyrrolidin-1-yl-5H-furan-2-ones to tetronic acids or unsaturated γ-lactones, see:
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Transformation of 4-pyrrolidin-1-yl-5H-furan-2-ones to tetronic acids or unsaturated γ-lactones, see: Farina F., Martin M.V., Martin-Aranda R.M., Guerenu A.M. Synth. Commun. 23:1993;459-472.
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(1993)
Synth. Commun.
, vol.23
, pp. 459-472
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Farina, F.1
Martin, M.V.2
Martin-Aranda, R.M.3
Guerenu, A.M.4
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9
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0028234807
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Nishide K., Aramata A., Kamanaka T., Inoue T., Node M. Tetrahedron. 50:1994;8337-8346.
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(1994)
Tetrahedron
, vol.50
, pp. 8337-8346
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Nishide, K.1
Aramata, A.2
Kamanaka, T.3
Inoue, T.4
Node, M.5
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14
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0001674525
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Synthesis of tetronic acid via other methods, see:
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Synthesis of tetronic acid via other methods, see: Svendsen A., Boll P.M. Tetrahedron. 29:1973;4251-4258.
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(1973)
Tetrahedron
, vol.29
, pp. 4251-4258
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-
Svendsen, A.1
Boll, P.M.2
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29
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33845376296
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For reviews of [2,3]-Wittig rearrangement, see:
-
For reviews of [2,3]-Wittig rearrangement, see: Nakai T., Mikami K. Chem. Rev. 86:1986;885-902.
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(1986)
Chem. Rev.
, vol.86
, pp. 885-902
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Nakai, T.1
Mikami, K.2
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30
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0000535071
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B.M. Trost, & I. Fleming. Oxford: Pergamon
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Marshall J.A. Trost B.M., Fleming I. Comprehensive Organic Synthesis. Vol. 3:1991;975-1014 Pergamon, Oxford.
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(1991)
Comprehensive Organic Synthesis
, vol.3
, pp. 975-1014
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Marshall, J.A.1
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31
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0000080952
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B.M. Trost, & I. Fleming. Oxford: Pergamon
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Marshall J.A. Trost B.M., Fleming I. Comprehensive Organic Synthesis. Vol. 6:1991;873-908 Pergamon, Oxford.
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(1991)
Comprehensive Organic Synthesis
, vol.6
, pp. 873-908
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Marshall, J.A.1
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33
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1242266853
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G. Helmchen, R.W. Hoffmann, J. Mulzer, & E. Schaumann. Stuttgart: Thieme
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Kallmerten J. Helmchen G., Hoffmann R.W., Mulzer J., Schaumann E. Houben-Weyl, Stereoselective Synthesis. Vol. E 21d:1995;3757-3809 Thieme, Stuttgart.
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(1995)
Houben-Weyl, Stereoselective Synthesis
, vol.21
, pp. 3757-3809
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Kallmerten, J.1
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36
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37049097355
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Barluenga J., Aznar F., Liz R., Bayod M. J. Chem. Soc., Chem. Commun. 1984;1427-1428.
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(1984)
J. Chem. Soc., Chem. Commun.
, pp. 1427-1428
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-
Barluenga, J.1
Aznar, F.2
Liz, R.3
Bayod, M.4
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37
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85030902058
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The crystal structure of compound anti-6e has been deposited at the Cambridge Crystallographic Data Centre as CCDC 212545.
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38
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0042458694
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Williard P.G., Tata J.R., Schlessinger R.H., Adams A.D., Iwanowicz E.J. J. Am. Chem. Soc. 110:1988;7901.
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(1988)
J. Am. Chem. Soc.
, vol.110
, pp. 7901
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Williard, P.G.1
Tata, J.R.2
Schlessinger, R.H.3
Adams, A.D.4
Iwanowicz, E.J.5
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39
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85030902145
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note
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a signal at 5.54 ppm.
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43
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1242334404
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G. Helmchen, R.W. Hoffmann, J. Mulzer, & E. Schaumann. Stuttgart: Thieme
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Kallmerten J. Helmchen G., Hoffmann R.W., Mulzer J., Schaumann E. Houben-Weyl, Stereoselective Synthesis. Vol. E 21d:1995;3810-3832 Thieme, Stuttgart.
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(1995)
Houben-Weyl, Stereoselective Synthesis
, vol.21
, pp. 3810-3832
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Kallmerten, J.1
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45
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0035898835
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Kitagawa O., Momose S.-I., Yamada Y., Shiro M., Taguchi T. Tetrahedron Lett. 42:2001;4865-4868.
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(2001)
Tetrahedron Lett.
, vol.42
, pp. 4865-4868
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Kitagawa, O.1
Momose, S.-I.2
Yamada, Y.3
Shiro, M.4
Taguchi, T.5
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46
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85030893701
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note
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Stereochemistries of compounds anti-6j and syn-6j were assigned by 2D-NOESY NMR experiments.
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47
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0033709722
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Compounds
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4 reduction of the coresponding α,β-unsaturated ester or aldehyde. For the synthesis of the α,β-unsaturated ester or aldehyde, see: Reizelman A., Scheren M., Nefkens G.H.L., Zwanenburg B. Synthesis. 2000;1944-1951.
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(2000)
Synthesis
, pp. 1944-1951
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Reizelman, A.1
Scheren, M.2
Nefkens, G.H.L.3
Zwanenburg, B.4
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49
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85030893145
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Geyer, B. P.; Mortimer, R. H. Shell Devel. Co. U.S. Patent 2,514,156, 1946.
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Shell Devel. Co. U.S. Patent 2,514,156, 1946
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Geyer, B.P.1
Mortimer, R.H.2
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50
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85030892245
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note
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1H NMR signals with syn-13c and anti-13c.
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51
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85030891581
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note
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The crystal structure of compounds syn-13b and syn-13c have been deposited at the Cambridge Crystallographic Data Centre as CCDC 212546 and CCDC 212547.
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