-
1
-
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0033549743
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-COR anion has been reported; see:
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-COR anion has been reported; see:. Hanzawa Y., Tabuchi N., Saito K., Noguchi S., and Taguchi T. Angew. Chem., Int. Ed. 38 (1999) 2395-2397
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(1999)
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Hanzawa, Y.1
Tabuchi, N.2
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Taguchi, T.5
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2
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0041378065
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Gröger H. Chem. Rev. 103 (2003) 2795-2827
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(2003)
Chem. Rev.
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Gröger, H.1
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4
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0038106171
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Bloch R. Chem. Rev. 98 (1998) 1407-1438
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Chem. Rev.
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Bloch, R.1
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7
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0000959887
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Utimoto K., Wakabayashi Y., Shishiyama Y., Inoue M., and Nozaki H. Tetrahedron Lett. 22 (1981) 4279-4280
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Tetrahedron Lett.
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Utimoto, K.1
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Inoue, M.4
Nozaki, H.5
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10
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0033547953
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-
2O-R type of structure:
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2O-R type of structure:. Nemoto H., Ibaragi T., Bando M., Kido M., and Shibuya M. Tetrahedron Lett. 40 (1999) 1319-1322
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(1999)
Tetrahedron Lett.
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Nemoto, H.1
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Kido, M.4
Shibuya, M.5
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19
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0000115729
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Yamamoto Y., Kubota Y., Honda Y., Fukui H., Asao N., and Nemoto H. J. Am. Chem. Soc. 116 (1994) 3161-3162
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Yamamoto, Y.1
Kubota, Y.2
Honda, Y.3
Fukui, H.4
Asao, N.5
Nemoto, H.6
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20
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0034629433
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Nemoto H., Ma R., Ibaragi T., Suzuki I., and Shibuya M. Tetrahedron 56 (2000) 1463-1468
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(2000)
Tetrahedron
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Nemoto, H.1
Ma, R.2
Ibaragi, T.3
Suzuki, I.4
Shibuya, M.5
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21
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0001342246
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Nemoto H., Ma R., Moriguchi H., Suzuki I., and Shibuya M. J. Organomet. Chem. 611 (2000) 445-448
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(2000)
J. Organomet. Chem.
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Nemoto, H.1
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Suzuki, I.4
Shibuya, M.5
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23
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0035843410
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Nemoto H., Ma R., Li X., Suzuki I., and Shibuya M. Tetrahedron Lett. 42 (2001) 2145-2147
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(2001)
Tetrahedron Lett.
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Nemoto, H.1
Ma, R.2
Li, X.3
Suzuki, I.4
Shibuya, M.5
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24
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0037213661
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Nemoto H., Li X., Ma R., Suzuki I., and Shibuya M. Tetrahedron Lett. 44 (2002) 73-75
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(2002)
Tetrahedron Lett.
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Nemoto, H.1
Li, X.2
Ma, R.3
Suzuki, I.4
Shibuya, M.5
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27
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33746915155
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Nemoto H., Ma R., Kawamura T., Kamiya M., and Shibuya M. J. Org. Chem. 71 (2006) 6038-6043
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(2006)
J. Org. Chem.
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Nemoto, H.1
Ma, R.2
Kawamura, T.3
Kamiya, M.4
Shibuya, M.5
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28
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33847616089
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Nemoto, H.; Takagaki, T.; Kubota, Y.; Yamamoto, Y. 1993, Unpublished result.
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29
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0028007403
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Bicyclic acetal moiety in 20 was prepared in an independent project:
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Bicyclic acetal moiety in 20 was prepared in an independent project:. Nemoto H. Tetrahedron Lett. 35 (1994) 7785-7788
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(1994)
Tetrahedron Lett.
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Nemoto, H.1
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30
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0842305159
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Nemoto H., Tsutsumi H., Yuzawa S., Peng X., Zhong W., Xie J., Miyoshi N., Suzuki I., and Shibuya M. Tetrahedron Lett. 45 (2004) 1667-1670
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Nemoto, H.1
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Yuzawa, S.3
Peng, X.4
Zhong, W.5
Xie, J.6
Miyoshi, N.7
Suzuki, I.8
Shibuya, M.9
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37
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0000574262
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Preparation of optically active 4-toluenesulfinimide:
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Preparation of optically active 4-toluenesulfinimide:. Davis F.A., Reddy R.T., Szewczyk J.M., Reddy G.V., Portonovo P.S., Zhang H., Fanelli D., Reddy R.T., Zhou P., and Carroll P.J. J. Org. Chem. 62 (1997) 2555-2563
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(1997)
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Davis, F.A.1
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Szewczyk, J.M.3
Reddy, G.V.4
Portonovo, P.S.5
Zhang, H.6
Fanelli, D.7
Reddy, R.T.8
Zhou, P.9
Carroll, P.J.10
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38
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0030694323
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Preparation of optically active tert-butanesulfinimide and deprotection of tert-butanesulfinyl group:
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Preparation of optically active tert-butanesulfinimide and deprotection of tert-butanesulfinyl group:. Liu G., Cogan D.A., and Ellman J.A. J. Am. Chem. Soc. 119 (1997) 9913-9914
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(1997)
J. Am. Chem. Soc.
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Liu, G.1
Cogan, D.A.2
Ellman, J.A.3
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39
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33847674002
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note
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18 as the major isomer by using TMSOTf, the relative stereochemistry of the sulfur and benzylic carbon of 24a is the same as that of 26a.
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41
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33847665117
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note
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1H NMR chart of crude 34 after step a, none of the diastereomer was observed. Therefore, racemization could occur during the following basic condition (step c).{A figure is presented}
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