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Laban, T.4
Schroen, M.5
Bräse, S.6
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representative recent examples: c) A. de Meijere, H. Nüske, M. Es-Sayed, T. Laban, M. Schroen, S. Bräse, Angew. Chem. 1999, 111, 3881-3884; Angew. Chem. Int. Ed. 1999, 38, 3669-3672;
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d) H. Paulsen, S. Antons, A. Brandes, M. Lögers, S. N. Müller, P. Naab, C. Schmeck, S. Schneider, J. Stoltefuß, Angew. Chem. 1999, 111, 3574-3576; Angew. Chem. Int. Ed. 1999, 38, 3373-3375;
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Schmeck, C.7
Schneider, S.8
Stoltefuß, J.9
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d) H. Paulsen, S. Antons, A. Brandes, M. Lögers, S. N. Müller, P. Naab, C. Schmeck, S. Schneider, J. Stoltefuß, Angew. Chem. 1999, 111, 3574-3576; Angew. Chem. Int. Ed. 1999, 38, 3373-3375;
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Michael additions have been frequently employed as initial step in domino reactions, for example: a) F. Näf, R. Decorzant, W. Thommen, Helv. Chim. Acta 1975, 58, 1808-1812;
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d) S. Saito, Y. Hirohara, O. Narahara, T. Moriwake, J. Am. Chem. Soc. 1989, 111, 4533-4535;
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e) T. Uyehara, N. Shida, Y. Yamamoto, J. Org. Chem. 1992, 57, 3139-3145;
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g) E. Yoshii, K. Hori, K. Nomura, K. Yamaguchi, Synlett 1995, 568-570;
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Synlett
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Yoshii, E.1
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h) J. G. Urones, N. M. Garrido, D. Diez, S. H. Dominguez, S. G. Davies, Tetrahedron: Asymmetry 1997, 8, 2683-2685;
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i) F. Dinon, E. Richards, P. J. Murphy, D. E. Hibbs, M. B. Hursthouse, K. M. A. Malik, Tetrahedron Lett. 1999, 40, 3279-3282;
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see also: c) W. C. Black, A. Giroux, G. Greidanus, Tetrahedron Lett. 1996, 37, 4471-4474;
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Black, W.C.1
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d) K. Tomooka, A. Nagasawa, Y. Wei, T. Nakai, Tetrahedron Lett. 1996, 37, 8899-8900.
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34
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b) Y. Yamamoto, S. Yamamoto, H. Yatagai, Y. Ishihara, K. Maruyama, J. Org. Chem. 1982, 47, 119-126.
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Ishihara, Y.4
Maruyama, K.5
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35
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0343705246
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note
-
All new compounds were fully characterized by NMR, IR, UV spectrscopy, and mass spectrometry, and gave correct combustion analyses or high-resolution mass spectra. The assignment of product configuration was accomplished by 2D and NOE-NMR data (see Supporting Information).
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37
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0347322788
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see also b) W. Oppolzer, R. J. Mills, W. Pachinger, T. Stevenson, Helv. Chim. Acta 1986, 69, 1542-1545;
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Oppolzer, W.1
Mills, R.J.2
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Stevenson, T.4
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c) D. R. Williams, W. S. Kissel, J. J. Li, Tetrahedron Lett. 1998, 39, 8593-8596.
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Williams, D.R.1
Kissel, W.S.2
Li, J.J.3
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39
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33845280186
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Charged dimethylaluminum imide complexes have been proposed and spectroscopically identified, see: a) D. A. Evans, K. T. Chapman, J. Bisaha, J. Am. Chem. Soc. 1988, 110, 1238-1256;
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Chapman, K.T.2
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33845554892
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D. A. Evans, M. D. Ennis, D. J. Mathre, J. Am. Chem. Soc. 1982, 104, 1737-1739.
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Ennis, M.D.2
Mathre, D.J.3
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43
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0343705242
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note
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3 addition and Swern oxidation.
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45
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0001359326
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A. Itoh, S. Ozawa, K. Oshima, H. Nozaki, Bull. Chem. Soc. Jpn. 1981, 54, 274-278.
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Itoh, A.1
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K. Maruoka, Y. Araki, H. Yamamoto, Tetrahedron Lett. 1988, 29, 3101-3104.
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Maruoka, K.1
Araki, Y.2
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47
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0001141046
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Excellent review: M. Arend, B. Westermann, N. Risch, Angew. Chem. 1998, 110, 1096-1122; Angew. Chem. Int. Ed. 1998, 37, 1044-1070.
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Arend, M.1
Westermann, B.2
Risch, N.3
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48
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0032482080
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Excellent review: M. Arend, B. Westermann, N. Risch, Angew. Chem. 1998, 110, 1096-1122; Angew. Chem. Int. Ed. 1998, 37, 1044-1070.
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