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1
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0017998510
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DMAP 1: Höfle, G.; Steglich, W.; Vorbrüggen, H. Angew. Chem., Int. Ed. Engl. 1978, 17, 569.
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DMAP 1: Höfle, G.; Steglich, W.; Vorbrüggen, H. Angew. Chem., Int. Ed. Engl. 1978, 17, 569.
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2
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0000305597
-
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NMI 2: Connors, K. A.; Pandit, N. K. Anal. Chem. 1978, 50, 1542.
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NMI 2: Connors, K. A.; Pandit, N. K. Anal. Chem. 1978, 50, 1542.
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3
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80051729483
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3 3: Vedejs, E.; Diver, S. T. J. Am. Chem. Soc. 1993, 115, 3358.
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3 3: Vedejs, E.; Diver, S. T. J. Am. Chem. Soc. 1993, 115, 3358.
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4
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0000926963
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Imidazolylidene carbenes 4: Grasa, G. A.; Kissling, R. M.; Nolan, S. P. Org. Lett. 2002, 4, 3583.
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5
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0000913836
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6
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0032868187
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TMEDA 5: Sano, T.; Ohashi, K.; Oriyama, T. Synthesis 1999, 1141.
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TMEDA 5: Sano, T.; Ohashi, K.; Oriyama, T. Synthesis 1999, 1141.
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7
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33846405667
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DBN 6 and THTP 7
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8
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50249134990
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For a recent review, see
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For a recent review, see: Denmark, S. E.; Beutner, G. L. Angew. Chem., Int. Ed. 2008, 47, 1560.
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9
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38349156051
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(a) Wurz, R. P
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Chiral NMI derivatives: Chiral DMAP derivatives
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Chiral DMAP derivatives: (a) Wurz, R. P. Chem. Rev. 2007, 107, 5570. Chiral NMI derivatives:
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10
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64349121606
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Miller, S. J. Acc. Chem. Res. 2004, 37, 601. Ishihara, K.; Kosugi, Y.; Akakura, M. J. Am. Chem. Soc. 2004, 126, 12212. Chiral phosphines:
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(b) Miller, S. J. Acc. Chem. Res. 2004, 37, 601. Ishihara, K.; Kosugi, Y.; Akakura, M. J. Am. Chem. Soc. 2004, 126, 12212. Chiral phosphines:
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11
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0242500932
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Chiral N-heterocyclic carbenes
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(c) Vedejs, E.; Daugulis, O. J. Am. Chem. Soc. 2003, 125, 4166. Chiral N-heterocyclic carbenes:
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Vedejs, E.1
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Enders, D.; Niemeier, O.; Henseler, A. Chem. Rev. 2007, 107, 5606. Marion, N.; Díez-González, S.; Nolan, S. P. Angew. Chem., Int. Ed. 2007, 46, 2988. Chiral vic-diamines:
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(d) Enders, D.; Niemeier, O.; Henseler, A. Chem. Rev. 2007, 107, 5606. Marion, N.; Díez-González, S.; Nolan, S. P. Angew. Chem., Int. Ed. 2007, 46, 2988. Chiral vic-diamines:
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13
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0032554989
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Chiral bicyclic amidines
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(e) Oriyama, T.; Imai, K.; Sano, T.; Hosoya, T. Tetrahedron Lett. 1998, 39, 3529. Chiral bicyclic amidines:
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Oriyama, T.1
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14
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4644304800
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Chiral bicyclic isothioureas
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(f) Birman, V. B.; Uffman, E. W.; Jiang, H.; Li, X.; Kilbane, C. J. J. Am. Chem. Soc. 2004, 126, 12226. Chiral bicyclic isothioureas:
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17
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64349122381
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Previously, catalytic kinetic resolution of amines has only been achieved using substituted 5-acyloxyoxazoles as stoichiometric acyl donors
-
Previously, catalytic kinetic resolution of amines has only been achieved using substituted 5-acyloxyoxazoles as stoichiometric acyl donors:
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18
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0035825126
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(a) Arai, S.; Bellemin-Laponnaz, S.; Fu, G. C. Angew Chem Int. Ed. 2001, 40, 234.
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Sabot, C.; Kumar, K. A.; Meunier, S.; Mioskowski, C. Tetrahedron Lett. 2007, 48, 3863. 2-Pyridinolate anion: (a) Nakamizo, N. Bull. Chem. Soc. Jpn. 1971, 2006. Cyanide anion:
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24
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64349092156
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Hoegberg, T.; Stroem, P.; Ebner, M.; Raemsby, S. J. Org. Chem. 1987, 52, 2033. Kabouche, Z.; Bruneau, C.; Dixneuf, P. H. Tetrahedron Lett. 1991, 32, 5359. HOBt anion:
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(b) Hoegberg, T.; Stroem, P.; Ebner, M.; Raemsby, S. J. Org. Chem. 1987, 52, 2033. Kabouche, Z.; Bruneau, C.; Dixneuf, P. H. Tetrahedron Lett. 1991, 32, 5359. HOBt anion:
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26
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0036161375
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84869270381
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a (19) = 8.7 were obtained through SciFinder.
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a (19) = 8.7 were obtained through SciFinder.
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30
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64349106403
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(a) Koecher, J.; Richter, F.; Laas, H.-J.; Wintermantel, M. PCT Int. Appl., WO 2002092658 A1, 2002.
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Kometani, H.1
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84869270382
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+), in DMSO at 5 mol % catalyst loading under conditions similar to those in Figure 5. Despite its lower activity, DBU triazolide, which is easily prepared in situ and soluble in common organic solvents, was used for the remainder of this study.
-
+), in DMSO at 5 mol % catalyst loading under conditions similar to those in Figure 5. Despite its lower activity, DBU triazolide, which is easily prepared in situ and soluble in common organic solvents, was used for the remainder of this study.
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33
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0001127818
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