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16
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58849100812
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-
note
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3, 100 MHz) δ (ppm): 159.95, 147.45, 133.32, 129.08, 128.80, 128.73, 86.64, 49.65, 44.33, 27.92. HRMS ESI(+): 326.0926 (calcd), 326.0961 (found).
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-
-
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17
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58849114082
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-
note
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3, 100 MHz) δ (ppm): 159.66, 147.46, 137.0, 128.62, 128.59, 127.81, 86.66, 54.55, 49.11, 27.93, 17.12.
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18
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0001392622
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and references cited therein
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Blaskovich M.A., Evindar G., Rose N.G.W., Wilkinson S., Luo Y., and Lajoie G.A. J. Org. Chem. 63 (1998) 3631-3646 and references cited therein
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21
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35048891074
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22
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23
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84987505887
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Seebach D., Juaristi E., Miller D.D., Schickli C., and Weber T. Helv. Chim. Acta 70 (1987) 237-261
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Seebach, D.1
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25
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58849103894
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note
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2-Ar)
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28
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42749088827
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Sagui F., Conti P., Roda G., Contestabile R., and Riva S. Tetrahedron 64 (2008) 5079-5084
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Sagui, F.1
Conti, P.2
Roda, G.3
Contestabile, R.4
Riva, S.5
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29
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34447285545
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Steinreiber J., Fesko K., Mayer C., Reisinger C., Schurmann M., and Griengl H. Tetrahedron 63 (2007) 8088-8093
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Steinreiber, J.1
Fesko, K.2
Mayer, C.3
Reisinger, C.4
Schurmann, M.5
Griengl, H.6
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30
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58849137857
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note
-
HPLC and NMR measurements showed a mixture of both syn diastereoisomers in equimolar quantities starting from this chiral sulfahydantoin 4 and propanal, isobutanal or benzaldehyde.
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31
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58849126885
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note
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3, 100 MHz) δ (ppm): 168.63, 133.96, 128.76, 128.54, 128.40, 73.47, 62.57, 44.91, 31.66, 18.63, 17.57.
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-
-
-
32
-
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58849162680
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note
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6, 100 MHz) δ (ppm): 170.94, 74.22, 64.25, 30.75, 19.14, 18.77.
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-
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34
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42549099415
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Walls A.B., Sickmann H.M., Brown A., Bouman S.D., Ransom B., Schousboe A., and Waagepetersen H.S. J. Neurochem. 105 (2008) 1462-1470
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Brown, A.3
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Ransom, B.5
Schousboe, A.6
Waagepetersen, H.S.7
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35
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41549097772
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and references cited therein
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Joo, J.-E.1
Pham, V.-T.2
Tian, Y.-S.3
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Oh, C.-Y.5
Lee, K.-Y.6
Ham, W.-H.7
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