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1
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33748739637
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Dissertation, Technische Universität Dresden
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H. Angert, Dissertation, Technische Universität Dresden, 1995.
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(1995)
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Angert, H.1
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4
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0001588647
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T. Kunz, A. Janowitz, H.-U. Reißig, Chem. Ber. 1989, 122, 2165-2175.
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(1989)
Chem. Ber.
, vol.122
, pp. 2165-2175
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Kunz, T.1
Janowitz, A.2
Reißig, H.-U.3
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5
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0000650354
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H.-U. Reißig, H. Angert, T. Kunz, A. Janowitz, G. Handke, E. Bruce-Adjei, J. Org. Chem. 1993, 58, 6280-6285.
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(1993)
J. Org. Chem.
, vol.58
, pp. 6280-6285
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Reißig, H.-U.1
Angert, H.2
Kunz, T.3
Janowitz, A.4
Handke, G.5
Bruce-Adjei, E.6
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6
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0000526442
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H. Angert, T. Kunz, H.-U. Reißig, Tetrahedron 1992, 48, 5681-5690.
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(1992)
Tetrahedron
, vol.48
, pp. 5681-5690
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Angert, H.1
Kunz, T.2
Reißig, H.-U.3
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8
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0005160858
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H. Angert, R. Schumacher, H.-U. Reißig, Chem. Ber. 1996, 129, 227-232.
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(1996)
Chem. Ber.
, vol.129
, pp. 227-232
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Angert, H.1
Schumacher, R.2
Reißig, H.-U.3
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11
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0001575276
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H.-U. Reißig, I. Reichelt, T. Kunz, Org. Synth. 1992, 71, 189-199.
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(1992)
Org. Synth.
, vol.71
, pp. 189-199
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Reißig, H.-U.1
Reichelt, I.2
Kunz, T.3
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18
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33748735481
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note
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1H-NMR spectroscopy.
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23
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0020046030
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D. H. R. Barton, M. Bénéchie, F. Khuong-Huu, P. Potier, V. Reyna-Pinedo, Tetrahedron Lett. 1982, 23, 651-654.
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(1982)
Tetrahedron Lett.
, vol.23
, pp. 651-654
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Barton, D.H.R.1
Bénéchie, M.2
Khuong-Huu, F.3
Potier, P.4
Reyna-Pinedo, V.5
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24
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0001553338
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G. E. Keck, M. B. Andrus, D. R. Romer, J. Org. Chem. 1991, 56, 417-420.
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(1991)
J. Org. Chem.
, vol.56
, pp. 417-420
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Keck, G.E.1
Andrus, M.B.2
Romer, D.R.3
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25
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0026098790
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M. Rodriguez, M. Llinares, S. Doulut, A. Heitz, J. Martinez, Tetrahedron Lett. 1991, 32, 923-926.
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(1991)
Tetrahedron Lett.
, vol.32
, pp. 923-926
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Rodriguez, M.1
Llinares, M.2
Doulut, S.3
Heitz, A.4
Martinez, J.5
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28
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33748726902
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note
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The configurational assignment of 11 is based on NMR arguments as presented in our earlier papers (see ref. [2-5]).
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30
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0026600311
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- See also: T. Nagai, G. Nishioka, M. Koyama, A. Ando, T. Miki, I. Kumadaki, Chem. Pharm. Bull. 1992, 40, 593-598.
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(1992)
Chem. Pharm. Bull.
, vol.40
, pp. 593-598
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Nagai, T.1
Nishioka, G.2
Koyama, M.3
Ando, A.4
Miki, T.5
Kumadaki, I.6
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33
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33748716001
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note
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The configurational assignment of the isomers was unequivocally possible by 2D-NOESY-NMR spectra.
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34
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0001316868
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(Eds.: B. M. Trost, I. Fleming), Pergamon Press, Oxford, Chapt. 2.4
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For Mukaiyama reactions of other benzyloxy substituted aldehydes, see: C. Gennari in Comprehensive Organic Synthesis (Eds.: B. M. Trost, I. Fleming), Pergamon Press, Oxford, 1991, Vol. 2, Chapt. 2.4.
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(1991)
Comprehensive Organic Synthesis
, vol.2
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Gennari, C.1
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35
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33751157459
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3. A. Rauk, I. R. Hunt, B. A. Keay, J. Org. Chem. 1994, 59, 6808-6816.
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(1994)
J. Org. Chem.
, vol.59
, pp. 6808-6816
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Rauk, A.1
Hunt, I.R.2
Keay, B.A.3
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37
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0028198510
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For exceptional results see: M. T. Reetz, K. Rölfing, N. Griebenow, Tetrahedron Lett. 1994, 35, 1969-1972.
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(1994)
Tetrahedron Lett.
, vol.35
, pp. 1969-1972
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Reetz, M.T.1
Rölfing, K.2
Griebenow, N.3
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41
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33748735609
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note
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Unfortunately, we were not able to prepare the corresponding dibenzylamino-protected aldehyde which is a highly promising candidate for stereoselective reactions.
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