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Recent examples for catalytic pinacol coupling system: (a) Zhang Y., Liu T. Synth. Commun. 18:1988;2173 (b) Léonard E., Duñach E., Périchon J. J. Chem. Soc., Chem. Commun. 1989;276 (c) Nomura R., Matsuno T., Endo T. J. Am. Chem. Soc. 118:1996;11666 (d) Lipski T.A., Hilfiker M.A., Nelson S.G. J. Org. Chem. 62:1997;4566 (e) Gansäuer A., Bauer D. J. Org. Chem. 63:1998;2070 (f) Groth U., Jeske M. Angew. Chem. Int. Ed. 39:2000;574.
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Recent examples for catalytic pinacol coupling system: (a) Zhang Y., Liu T. Synth. Commun. 18:1988;2173 (b) Léonard E., Duñach E., Périchon J. J. Chem. Soc., Chem. Commun. 1989;276 (c) Nomura R., Matsuno T., Endo T. J. Am. Chem. Soc. 118:1996;11666 (d) Lipski T.A., Hilfiker M.A., Nelson S.G. J. Org. Chem. 62:1997;4566 (e) Gansäuer A., Bauer D. J. Org. Chem. 63:1998;2070 (f) Groth U., Jeske M. Angew. Chem. Int. Ed. 39:2000;574.
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Recent examples for catalytic pinacol coupling system: (a) Zhang Y., Liu T. Synth. Commun. 18:1988;2173 (b) Léonard E., Duñach E., Périchon J. J. Chem. Soc., Chem. Commun. 1989;276 (c) Nomura R., Matsuno T., Endo T. J. Am. Chem. Soc. 118:1996;11666 (d) Lipski T.A., Hilfiker M.A., Nelson S.G. J. Org. Chem. 62:1997;4566 (e) Gansäuer A., Bauer D. J. Org. Chem. 63:1998;2070 (f) Groth U., Jeske M. Angew. Chem. Int. Ed. 39:2000;574.
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Recent examples for catalytic pinacol coupling system: (a) Zhang Y., Liu T. Synth. Commun. 18:1988;2173 (b) Léonard E., Duñach E., Périchon J. J. Chem. Soc., Chem. Commun. 1989;276 (c) Nomura R., Matsuno T., Endo T. J. Am. Chem. Soc. 118:1996;11666 (d) Lipski T.A., Hilfiker M.A., Nelson S.G. J. Org. Chem. 62:1997;4566 (e) Gansäuer A., Bauer D. J. Org. Chem. 63:1998;2070 (f) Groth U., Jeske M. Angew. Chem. Int. Ed. 39:2000;574.
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Lipski, T.A.1
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Nelson, S.G.3
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0039750771
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Recent examples for catalytic pinacol coupling system: (a) Zhang Y., Liu T. Synth. Commun. 18:1988;2173 (b) Léonard E., Duñach E., Périchon J. J. Chem. Soc., Chem. Commun. 1989;276 (c) Nomura R., Matsuno T., Endo T. J. Am. Chem. Soc. 118:1996;11666 (d) Lipski T.A., Hilfiker M.A., Nelson S.G. J. Org. Chem. 62:1997;4566 (e) Gansäuer A., Bauer D. J. Org. Chem. 63:1998;2070 (f) Groth U., Jeske M. Angew. Chem. Int. Ed. 39:2000;574.
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Bauer, D.2
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Recent examples for catalytic pinacol coupling system: (a) Zhang Y., Liu T. Synth. Commun. 18:1988;2173 (b) Léonard E., Duñach E., Périchon J. J. Chem. Soc., Chem. Commun. 1989;276 (c) Nomura R., Matsuno T., Endo T. J. Am. Chem. Soc. 118:1996;11666 (d) Lipski T.A., Hilfiker M.A., Nelson S.G. J. Org. Chem. 62:1997;4566 (e) Gansäuer A., Bauer D. J. Org. Chem. 63:1998;2070 (f) Groth U., Jeske M. Angew. Chem. Int. Ed. 39:2000;574.
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Some examples for Zn-promoted reduction under acid-free conditions: (a) Toda F., Tanaka K., Tange H. J. Chem. Soc., Perkin Trans. 1. 1989;1555 (b) Sadavarte V.S., Swami S.S., Desai D.G. Synth. Commun. 28:1998;1139 (c) Kardile G.B., Desai D.G., Swami S.S. Synth. Commun. 29:1999;2129.
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Some examples for Zn-promoted reduction under acid-free conditions: (a) Toda F., Tanaka K., Tange H. J. Chem. Soc., Perkin Trans. 1. 1989;1555 (b) Sadavarte V.S., Swami S.S., Desai D.G. Synth. Commun. 28:1998;1139 (c) Kardile G.B., Desai D.G., Swami S.S. Synth. Commun. 29:1999;2129.
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Some examples for Zn-promoted reduction under acid-free conditions: (a) Toda F., Tanaka K., Tange H. J. Chem. Soc., Perkin Trans. 1. 1989;1555 (b) Sadavarte V.S., Swami S.S., Desai D.G. Synth. Commun. 28:1998;1139 (c) Kardile G.B., Desai D.G., Swami S.S. Synth. Commun. 29:1999;2129.
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2O is treated with PhCHO at once, reductive esterification does not proceed effectively
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2O is treated with PhCHO at once, reductive esterification does not proceed effectively.
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42
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84966129786
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