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This work was supported by the Deutsche Forschungsgemeinschaft, the Fonds der Chemischen Industrie, and Fa. E. Merck, Darmstadt.-Glycosylimidates, Part 79. For Part 78, see T.G. Mayer, R.R. Schmidt, Liebigs Ann., submitted
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1. This work was supported by the Deutsche Forschungsgemeinschaft, the Fonds der Chemischen Industrie, and Fa. E. Merck, Darmstadt.-Glycosylimidates, Part 79. For Part 78, see T.G. Mayer, R.R. Schmidt, Liebigs Ann., submitted.
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19. Employing the nitrile effect for anomeric stereocontrol: R.R. Schmidt, M. Behrendt, A. Toepfer, Synlett 1990, 694-696; Y.D. Vankar, P.S. Vankar, M. Behrendt, R.R. Schmidt, Tetrahedron 1991, 47, 9985-9988.
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19. Employing the nitrile effect for anomeric stereocontrol: R.R. Schmidt, M. Behrendt, A. Toepfer, Synlett 1990, 694-696; Y.D. Vankar, P.S. Vankar, M. Behrendt, R.R. Schmidt, Tetrahedron 1991, 47, 9985-9988.
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21. R.R. Schmidt, P. Zimmermann, Angew. Chem. 1986, 98, 722-723; Angew. Chem. Int. Ed. Engl. 1986, 25, 725-726; P. Zimmermann, R. Bommer, T. Bär, R.R. Schmidt, J. Carbohydr. Chem. 1988, 7, 435-452.
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33
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0001235855
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22. Details of the structural assignment by NMR have been reported: A. Geyer, G. Hummel, T. Eisele, S. Reinhardt, R.R. Schmidt, Chem. Eur. J., 1996, 2, 981-988.
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Geyer, A.1
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34
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0011431052
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note
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1i,2i = 3.5 Hz, 1i-H).
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