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7
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Schmalz H.G. (Ed), Wiley-VCH, Weinheim
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Schuppan, J.1
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Takahashi, H.1
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Imai, N.1
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36
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0001553673
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Diastereoselective Simmons-Smith cyclopropanation with a sugar auxiliary:
-
Diastereoselective Simmons-Smith cyclopropanation with a sugar auxiliary:. Charette A.B., Cote B., and Marcoux J.-F. J. Am. Chem. Soc. 113 (1991) 8166-8167
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Charette, A.B.1
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43
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0001123797
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Diastereoselective Simmons-Smith cyclopropanation with a chiral diol auxiliary:
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Diastereoselective Simmons-Smith cyclopropanation with a chiral diol auxiliary:. Arai I., Mori A., and Yamamoto H. J. Am. Chem. Soc. 107 (1985) 8254-8256
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Arai, I.1
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0001423540
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Mori A., Arai I., Yamamoto H., Nakai H., and Arai Y. Tetrahedron 42 (1986) 6447-6458
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Mori, A.1
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Yamamoto, H.3
Nakai, H.4
Arai, Y.5
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50
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10744227607
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Sugimura T., Futagawa T., Yoshikawa M., Katagiri T., Miyashige R., Mizuguchi M., Nagano S., Sugimori S., Tai A., Tei T., and Okumura T. Tetrahedron 52 (2001) 7495-7499
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Sugimura, T.1
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Mizuguchi, M.6
Nagano, S.7
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Tai, A.9
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Tei T., Sugimura T., Katagiri T., Tai A., and Okuyama T. Tetrahedron: Asymmetry 12 (2001) 2727-2730
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Tei, T.1
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Tai, A.4
Okuyama, T.5
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52
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0032556392
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Diastereoselective Simmons-Smith cyclopropanation with camphor auxiliary:
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Diastereoselective Simmons-Smith cyclopropanation with camphor auxiliary:. Kaye P.T., and Molema W.E. Chem. Commun. (1998) 2479-2480
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Kaye, P.T.1
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53
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33751553350
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Diastereoselective Simmons-Smith cyclopropanation with a chiral boronic acid ester auxiliary:
-
Diastereoselective Simmons-Smith cyclopropanation with a chiral boronic acid ester auxiliary:. Imai T., Mineta H., and Nishida S. J. Org. Chem. 55 (1990) 4986-4988
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Imai, T.1
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55
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0344065681
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Diastereoselective Simmons-Smith cyclopropanation with an ephedrine auxiliary:
-
Diastereoselective Simmons-Smith cyclopropanation with an ephedrine auxiliary:. Aggarwal V.K., Fang G.Y., and Meek G. Org. Lett. 5 (2003) 4417-4430
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Aggarwal, V.K.1
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Meek, G.3
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56
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11144357353
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Diastereoselective Simmons-Smith cyclopropanation:
-
Diastereoselective Simmons-Smith cyclopropanation:. Corsaro A., Chiacchio U., Adamo R., Pistara V., Rescifina A., Romeo R., Catelani G., D'Andrea F., Mariani M., and Attolino E. Tetrahedron 60 (2004) 3787-3795
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Corsaro, A.1
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Adamo, R.3
Pistara, V.4
Rescifina, A.5
Romeo, R.6
Catelani, G.7
D'Andrea, F.8
Mariani, M.9
Attolino, E.10
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Silverman, R.B.1
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60
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0345412537
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Black, S.L.1
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Grundt, P.3
Miller, C.N.4
Wood, S.5
Traynor, J.R.6
Lewis, J.W.7
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0034671064
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Charette, A.B.1
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Xie, Y.5
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78
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0037035617
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Katagiri, T.1
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Uneyama, K.5
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80
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34250656871
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Functional group transformations at α-carbon to trifluoromethyl group
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The bulkiness of the trifluoromethyl group in the stereoselective reductions was sometimes comparable to that of a phenyl group, see:. Fluorine-Containing Synthons. Soloshonok V. (Ed), ACS, Washington, DC
-
The bulkiness of the trifluoromethyl group in the stereoselective reductions was sometimes comparable to that of a phenyl group, see:. Katagiri T., and Uneyama K. Functional group transformations at α-carbon to trifluoromethyl group. In: Soloshonok V. (Ed). Fluorine-Containing Synthons. ACS Symposium Series 911 (2005), ACS, Washington, DC 318-341
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Katagiri, T.1
Uneyama, K.2
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0003481072
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Synthesis of stereochemically defined trifluoromethyl-containing compounds through (S)-3,3,3-trifluoropropene oxide
-
Soloshonok V.A. (Ed), Wiley, Chichester
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Katagiri T. Synthesis of stereochemically defined trifluoromethyl-containing compounds through (S)-3,3,3-trifluoropropene oxide. In: Soloshonok V.A. (Ed). Enantiocontrolled Synthesis of Fluoro-Organic Compounds: Stereochemical Challenges and Biomedicinal Targets (1999), Wiley, Chichester 161-178
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Katagiri, T.1
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86
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0037138704
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Schaus S.E., Brandes B.D., Larrow J.F., Tokunaga M., Hansen K.B., Gould A.E., Furrow M.E., and Jacobsen E.N. J. Am. Chem. Soc. 124 (2002) 1307-1315
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Schaus, S.E.1
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Hansen, K.B.5
Gould, A.E.6
Furrow, M.E.7
Jacobsen, E.N.8
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87
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33646839762
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note
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2 = 0.1772 for all reflections. Crystallographic data for the structure herein have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 602550. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK [fax: +44(0) 1223 336033 or e-mail: deposit@ccdc.cam.ac.uk].
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