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For a leading reference in this area see: Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Berlin, 1999.
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For recent examples, see: (a) Bolm, C.; Kesselgruber, M.; Hermanns, N.; Hildebrand, J. P.; Raabe, G. Angew. Chem. 2001, 113, 1536; Angew. Chem., Int. Ed. 2001, 40, 1488.
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For this reaction, see: Njar, V. C. O. Synthesis 2000, 2019.
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Njar, V.C.O.1
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46
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0037948315
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-
note
-
2 as reducing agent, ca. 50% conversion was achieved after 24 h at -10 °C. Hydrolysis of the resulting silyl ethers with catalytic amounts of p-TosOH afforded the corresponding alcohols, alas as racemates.
-
-
-
-
50
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0038285626
-
Gensin
-
Hall, S. R., du Boulay, D. J., Olthof-Hazekamp, R., Eds.; University of Western Australia
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Subramanian, V.; Hall, S. R. GENSIN; Hall, S. R., du Boulay, D. J., Olthof-Hazekamp, R., Eds.; Xtal3.7 System; University of Western Australia, 2000.
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Xtal3.7 System
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Subramanian, V.1
Hall, S.R.2
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51
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0037948311
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Gentan
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Hall, S. R., du Boulay, D. J., Olthof-Hazekamp, R., Eds.; University of Western Australia
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Hall, S. R. GENTAN; Hall, S. R., du Boulay, D. J., Olthof-Hazekamp, R., Eds.; Xtal3.7 System; University of Western Australia, 2000.
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Xtal3.7 System;
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Hall, S.R.1
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