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10
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85034344587
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WO 016583
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J.-M. Gaudin, WO 016583, 2009.
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Gaudin, J.-M.1
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D. Ye J. Wang X. Zhang Y. Zhou X. Ding E. Feng H. Sun G. Liu H. Jiang H. Liu Green Chem. 2009 11 1201-1208.
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Feng, E.6
Sun, H.7
Liu, G.8
Jiang, H.9
Liu, H.10
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26
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85034310686
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-
For instance, the reaction of phenylisocyanate with pyrryl potassium afforded selectively 1-phenylaminocarbonyl pyrrole, while the analogous reaction with pyrryl magnesium bromide gave a mixture of 1- and 2-phenylaminocarbonyl pirrole.10a
-
For instance, the reaction of phenylisocyanate with pyrryl potassium afforded selectively 1-phenylaminocarbonyl pyrrole, while the analogous reaction with pyrryl magnesium bromide gave a mixture of 1- and 2-phenylaminocarbonyl pirrole.10a.
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29
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74549167367
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Via ethylisocyanate
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Via ethylisocyanate: N. Goyal Synlett 2010 335-336.
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Goyal, N.1
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Ballivet-Tkatchenko, D.1
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58149336789
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X. Fu Z. Zhang C. Li L. Wang H. Ji Y. Yang T. Zou G. Gao Catal. Commun. 2009 10 665-668.
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T. Baba M. Fujiwara A. Oosaku A. Kobayashi R. G. Deleon Y. Ono Appl. Catal., A 2002 227 1-6.
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Baba, T.1
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67
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85034369400
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-
2O, alcohols, acetone, was prevented by the poor substrate solubility and/or the chemical behavior of the reactants in these media
-
2O, alcohols, acetone, was prevented by the poor substrate solubility and/or the chemical behavior of the reactants in these media.
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70
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85034320146
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-
+), 224 (M − OPh), 210, 132, 91, 77, 65, 39
-
+), 224 (M − OPh), 210, 132, 91, 77, 65, 39.
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-
-
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71
-
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85034331685
-
-
2Et (8.7)27 in the same solvent (DMSO), it can be reasonably inferred that DBU is a stronger base than the L-leucine methyl ester
-
2Et (8.7)27 in the same solvent (DMSO), it can be reasonably inferred that DBU is a stronger base than the L-leucine methyl ester.
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72
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33749144042
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-
R. Schwesinger H. Schlemper C. Hasenfratz J. Willaredt T. Dambacher T. Breuer C. Ottaway M. Fletschinger J. Boele H. Fritz D. Putzas H. W. Rotter F. G. Bordwell A. V. Satish G.-Z. Ji E. M. Peters H. G. Von Schnering L. Walz Liebigs Ann. 1996 1055-1081.
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(1996)
Liebigs Ann.
, pp. 1055-1081
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Schwesinger, R.1
Schlemper, H.2
Hasenfratz, C.3
Willaredt, J.4
Dambacher, T.5
Breuer, T.6
Ottaway, C.7
Fletschinger, M.8
Boele, J.9
Fritz, H.10
Putzas, D.11
Rotter, H.W.12
Bordwell, F.G.13
Satish, A.V.14
Ji, G.-Z.15
Peters, E.M.16
Von Schnering, H.G.17
Walz, L.18
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74
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85034347257
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-
Polarimetric measurements on isolated urea 10 have shown that the ureidization process was accompanied by extended racemization of the chiral center of the amino ester moiety
-
Polarimetric measurements on isolated urea 10 have shown that the ureidization process was accompanied by extended racemization of the chiral center of the amino ester moiety.
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-
-
-
76
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85034385925
-
-
5N), 137, 111, 94, 80, 67, 42
-
5N), 137, 111, 94, 80, 67, 42.
-
-
-
-
77
-
-
85034316481
-
-
+), 281, 256, 213, 184, 170, 156, 146, 128, 104, 94, 77, 68, 51, 39
-
+), 281, 256, 213, 184, 170, 156, 146, 128, 104, 94, 77, 68, 51, 39.
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