-
6
-
-
38349044563
-
-
Recent examples focusing on conformational change by incorporation of a few fluorine atoms:
-
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7
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9944242396
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Molteni M., Pesenti C., Sani M., Volonterio A., and Zanda M. J. Fluorine Chem. 125 (2005) 1735
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Belleney, J.1
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14
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15
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0026027887
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Watanabe J., Tokuyama S., Takahashi M., Kaneto H., Maeda M., Kawasaki K., Taguchi T., Kobayashi Y., Yamamoto Y., and Shimokawa K. J. Pharmacobiodyn. 14 (1991) 101
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19
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0033550301
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Kunishima M., Kawachi C., Morita J., Terao K., Iwasaki F., and Tani S. Tetrahedron 55 (1999) 13159
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Kunishima, M.1
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20
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0035906028
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Kunishima M., Kawachi C., Hioki K., Terao K., and Tani S. Tetrahedron 57 (2001) 1551
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Tetrahedron
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Kunishima, M.1
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21
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0037193109
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Kunishima M., Hioki K., Wada A., Kobayashi H., and Tani S. Tetrahedron Lett. 43 (2002) 3323
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Kunishima, M.1
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-
23
-
-
38349040111
-
-
note
-
Because DMT-MM is quantitatively prepared just by mixing CDMT with NMM in THF, addition of 1.1 equiv of DMT-MM and NMM is equal to combination of 1.1 equiv of CDMT and 2.2 equiv of NMM.
-
-
-
-
24
-
-
0003998388
-
-
a values of 9.99, 15.5, and 12.37 at 25 °C, respectively:. Lide D.R. (Ed), CRC, Boca Raton, FL
-
a values of 9.99, 15.5, and 12.37 at 25 °C, respectively:. In: Lide D.R. (Ed). CRC Handbook of Chemistry and Physics. 82nd ed. (2001), CRC, Boca Raton, FL
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(2001)
CRC Handbook of Chemistry and Physics. 82nd ed.
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-
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25
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34247108511
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Abraham M.H., Grellier P.L., Prior D.V., Duce P.P., Morris J.J., and Taylor P.J. J. Chem. Soc., Perkin Trans. 2 (1989) 699
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Abraham, M.H.1
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26
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37049073393
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Abraham M.H., Grellier P.L., Prior D.V., Morris J.J., and Taylor P.J. J. Chem. Soc., Perkin Trans. 2 (1990) 521
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27
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15744375697
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Gaussian, Wallingford, CT
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Frisch M.J., Trucks G.W., Schlegel H.B., Scuseria G.E., Robb M.A., Cheeseman J.R., Montgomery Jr. J.A., Vreven T., Kudin K.N., Burant J.C., Millam J.M., Iyengar S.S., Tomasi J., Barone V., Mennucci B., Cossi M., Scalmani G., Rega N., Petersson G.A., Nakatsuji H., Hada M., Ehara M., Toyota K., Fukuda R., Hasegawa J., Ishida M., Nakajima T., Honda Y., Kitao O., Nakai H., Klene M., Li X., Knox J.E., Hratchian H.P., Cross J.B., Bakken V., Adamo C., Jaramillo J., Gomperts R., Stratmann R.E., Yazyev O., Austin A.J., Cammi R., Pomelli C., Ochterski J.W., Ayala P.Y., Morokuma K., Voth G.A., Salvador P., Dannenberg J.J., Zakrzewski V.G., Dapprich S., Daniels A.D., Strain M.C., Farkas O., Malick D.K., Rabuck A.D., Raghavachari K., Foresman J.B., Ortiz J.V., Cui Q., Baboul A.G., Clifford S., Cioslowski J., Stefanov B.B., Liu G., Liashenko A., Piskorz P., Komaromi I., Martin R.L., Fox D.J., Keith T., Al-Laham M.A., Peng C.Y., Nanayakkara A., Challacombe M., Gill P.M.W., Johnson B., Chen W., Wong M.W., Gonzalez C., and Pople J.A. Gaussian 03, Revision B.03 (2004), Gaussian, Wallingford, CT
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Gaussian 03, Revision B.03
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Frisch, M.J.1
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Li, X.32
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Hratchian, H.P.34
Cross, J.B.35
Bakken, V.36
Adamo, C.37
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Gomperts, R.39
Stratmann, R.E.40
Yazyev, O.41
Austin, A.J.42
Cammi, R.43
Pomelli, C.44
Ochterski, J.W.45
Ayala, P.Y.46
Morokuma, K.47
Voth, G.A.48
Salvador, P.49
Dannenberg, J.J.50
Zakrzewski, V.G.51
Dapprich, S.52
Daniels, A.D.53
Strain, M.C.54
Farkas, O.55
Malick, D.K.56
Rabuck, A.D.57
Raghavachari, K.58
Foresman, J.B.59
Ortiz, J.V.60
Cui, Q.61
Baboul, A.G.62
Clifford, S.63
Cioslowski, J.64
Stefanov, B.B.65
Liu, G.66
Liashenko, A.67
Piskorz, P.68
Komaromi, I.69
Martin, R.L.70
Fox, D.J.71
Keith, T.72
Al-Laham, M.A.73
Peng, C.Y.74
Nanayakkara, A.75
Challacombe, M.76
Gill, P.M.W.77
Johnson, B.78
Chen, W.79
Wong, M.W.80
Gonzalez, C.81
Pople, J.A.82
more..
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28
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37049075389
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Soloshonok V.A., Kukhar' V.P., Galushko S.V., Svistunova N.Y., Avilov D.V., Kuz'mina N.A., Raevski N.I., Struchkov Y.T., Pysarevsky A.P., and Belokon' Y.N. J. Chem. Soc., Perkin Trans. 1 (1993) 3143
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Raevski, N.I.7
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Pysarevsky, A.P.9
Belokon', Y.N.10
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29
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0029163546
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-
Soloshonok V.A., Avilov D.V., Kukhar' V.P., Tararov V.I., Savel'eva T.F., Churkina T.D., Ikonnikov N.S., Kochetkov K.A., Orlova S.A., Pysarevsky A.P., Struchkov Y.T., Raevski N.I., and Belokon' Y.N. Tetrahedron: Asymmetry 6 (1995) 1741
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Struchkov, Y.T.11
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Belokon', Y.N.13
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30
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Belokon' Y.N., Tararov V.I., Maleev V.I., Savel'eva T.F., and Ryzhov M.G. Tetrahedron: Asymmetry 9 (1998) 4249
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Belokon', Y.N.1
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32
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0021818109
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Scolastico C., Conca E., Prati L., Guanti G., Banfi L., Berti A., Farina P., and Valcavi U. Synthesis (1985) 850
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Synthesis
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Valcavi, U.8
-
33
-
-
38349040112
-
-
note
-
3-Thr-OBn. Because of the presence of inseparable impurity, three sets of doublets were observed from this mixture. Calculation of the de value using the most and the second largest peaks afforded 96.0% de, which apparently guaranteed the minimum level of diastereoselectivity.
-
-
-
-
34
-
-
38349065620
-
-
note
-
19F NMR, and a similar calculation as in Ref. 17 afforded 91.7% ee as the minimum level of enantioselectivity.
-
-
-
-
37
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0035968915
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Chakraborty T.K., Ghosh A., Nagaraj R., Sankar A.R., and Kunwar A.C. Tetrahedron 57 (2001) 9169
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