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84871099070
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Reviews
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Reviews
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2
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0003394220
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John Wiely & Sons, Inc. New York
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M. P. Doyle, M. A. McKervey, T. Ye, Modern Catalytic Methods for Organic Synthesis with Diazo Compounds, John Wiely & Sons, Inc., New York, 1997
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(1997)
Modern Catalytic Methods for Organic Synthesis with Diazo Compounds
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Doyle, M.P.1
McKervey, M.A.2
Ye, T.3
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6
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0038222536
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for a specific example, see
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H. Lebel, J.-F. Marcoux, C. Molinaro, A. B. Charette, Chem. Rev. 2003, 103, 977-1050; for a specific example, see
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Chem. Rev.
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Lebel, H.1
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S. M. Berberich, R. J. Cherney, J. Colucci, C. Courillon, L. S. Geraci, T. A. Kirkland, M. A. Marx, M. F. Schneider, S. F. Martin, Tetrahedron 2003, 59, 6819-6832.
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Berberich, S.M.1
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Schneider, M.F.8
Martin, S.F.9
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9
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84871059432
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For transition metal catalysts, see
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For transition metal catalysts, see
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10
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0001080522
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M. P. Doyle, R. E. Austin, A. S. Bailey, M. P. Dwyer, A. B. Dyatkin, A. V. Kalinin, M. M. Y. Kwan, S. Liras, C. J. Oalmann, R. J. Pieters, M. N. Protopopova, C. E. Raab, G. H. P. Roos, Q.-L. Zhou, S. F. Martin, J. Am. Chem. Soc. 1995, 117, 5763-5775
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Kalinin, A.V.6
Kwan, M.M.Y.7
Liras, S.8
Oalmann, C.J.9
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Protopopova, M.N.11
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0028861083
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S.-B. Park, K. Murata, H. Matsumoto, H. Nishiyama, Tetrahedron: Asymmetry 1995, 6, 2487-2494
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D.-J. Cho, S.-J. Jeon, H.-S. Kim, C.-S. Cho, S.-C. Shim, T.-J. Kim, Tetrahedron: Asymmetry 1999, 10, 3833-3848
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M. P. Doyle, W. Hu, B. Chapman, A. B. Marnett, C. S. Peterson, J. P. Vitale, S. A. Stanley, J. Am. Chem. Soc. 2000, 122, 5718-5728
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M. P. Doyle, S. B. Davies, W. Hu, Org. Lett. 2000, 2, 1145-1147
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T. Uchida, B. Saha, T. Katsuki, Tetrahedron Lett. 2001, 42, 2521-2524
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0034794315
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C.-M. Che, J.-S. Huang, F.-W. Lee, Y. Li, T.-S. Lai, H.-L. Kwong, P.-F. Teng, W.-S. Lee, W.-C. Lo, S.-M. Peng, Z.-Y. Zhou, J. Am. Chem. Soc. 2001, 123, 4119-4129
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Che, C.-M.1
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B. Saha, T. Uchida, T. Katsuki, Tetrahedron: Asymmetry 2003, 14, 823-836
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Z.-J. Xu, R. Fang, C. Zhao, J.-S. Huang, G.-Y. Li, N. Zhu, C.-M. Che, J. Am. Chem. Soc. 2009, 131, 4405-4417
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C.-M. Ho, J.-L. Zhang, C.-Y. Zhou, O.-Y. Chan, J. J. Yan, F.-Y. Zhang, J.-S. Huang, C.-M. Che, J. Am. Chem. Soc. 2010, 132, 1886-1894
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24
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33644879985
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for organocatalysts, see
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C. Escudero, J. Pérez-Prieto, S.-E. Stiriba, Inorg. Chim. Acta 2006, 359, 1974-1978; for organocatalysts, see
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(2006)
Inorg. Chim. Acta
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N. Bremeyer, S. C. Smith, S. V. Ley, M. J. Gaunt, Angew. Chem. 2004, 116, 2735-2738
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(2004)
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C. C. C. Johansson, N. Bremeyer, S. V. Ley, D. R. Owen, S. C. Smith, M. J. Gaunt, Angew. Chem. 2006, 118, 6170-6175
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33748765777
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for the stoichiometric process, see
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Angew. Chem. Int. Ed. 2006, 45, 6024-6028; for the stoichiometric process, see
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(2006)
Angew. Chem. Int. Ed.
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Paris, J.-M.3
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84871097858
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For examples of cyclopropanation reactions in water with achiral catalysts, see
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For examples of cyclopropanation reactions in water with achiral catalysts, see
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31
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0035977228
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A. G. M. Barrett, D. C. Braddock, I. Lenoir, H. Tone, J. Org. Chem. 2001, 66, 8260-8263
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[3m]
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[3m]
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84871069315
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[3q]; conversely a few catalytic systems have been developed to perform enantioselective intermolecular cyclopropanation reactions, for a review, see
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[3q]; conversely a few catalytic systems have been developed to perform enantioselective intermolecular cyclopropanation reactions, for a review, see
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34
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T. Ikeno, A. Nishizuka, M. Sato, T. Yamada, Synlett 2001, 406-408
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43
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For the preparation of Ru(II)-Pheox complexes 4, 5 and 6, see the Supporting Information.
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For the preparation of Ru(II)-Pheox complexes 4, 5 and 6, see the Supporting Information.
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44
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