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11
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19944427998
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-
Sitagliptin: D. Kim, L. Wang, M. Beconi, G.J. Eiermann, M.H. Fisher, H. He, G.J. Hickey, J.E. Kowalchick, B.E. Leiting, K. Lyons, F. Marsilio, M.E. McCann, R.A. Patel, A. Petrov, G. Scapin, S.B. Patel, R.S. Roy, J.K. Wu, M.J. Wyvratt, B.B. Zhang, L. Zhu, N.A. Thornberry, and A.E. Weber J. Med. Chem. 48 2005 141
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12
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0037777695
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13
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22744449063
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-
Saxagliptin: D.J. Augeri, J.A. Robl, D.A. Betebenner, D.R. Magnin, A. Khanna, J.G. Robertson, L.M. Simpkins, P.C. Taunk, Q. Huang, S.-P. Han, B. Abboa-Offei, A. Wang, M. Cap, L. Xin, L. Tao, E. Tozzo, G.E. Welzel, B.A. Biller, M.S. Kirby, R.A. Parker, and L.G. Hamann J. Med. Chem. 48 2005 5025
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14
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34248999413
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Alogliptin: J. Feng, Z. Zhang, M.W. Wallace, J.A. Stafford, S.W. Kaldor, D.B. Kassel, M. Navre, L. Shi, R.J. Skene, T. Asakawa, K. Takeuchi, R. Xu, D.R. Webb, and S.L. Gwaltney II J. Med. Chem. 50 2007 2297
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15
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75649128008
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57649225147
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19
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77955367308
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20
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1942532946
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J. Clayden, Elsevier Amsterdam
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Atropisomerism J. Clayden, Tetrahedron Symposia-In-Print Vol. 60 2004 Elsevier Amsterdam 4335 4558
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21
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77957871155
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Compound 17 was obtained in 94% purity
-
Compound 17 was obtained in 94% purity.
-
-
-
-
22
-
-
77957867677
-
-
+ 413.0
-
+ 413.0.
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23
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0033780088
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Gorrell, M.D.6
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24
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10644284275
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Y.-S. Chen, C.-H. Chien, C.M. Goparaju, J.T.-A. Hsu, P.-H. Liang, and X. Chen Protein Expr. Purif. 35 2004 142
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Chen, Y.-S.1
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Chen, X.6
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12444313913
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Chang, S.-P.7
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Chen, X.9
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26
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25844459084
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G.R. Lankas, B. Leiting, R.S. Roy, G.J. Eiermann, M.G. Beconi, T. Biftu, C.-C. Chan, S. Edmundson, W.P. Feeney, H. He, D.E. Ippolito, D. Kim, K.A. Lyons, H.O. Ok, R.A. Patel, A.N. Petrov, K.A. Pryor, X. Qian, L. Reigle, A. Woods, J.K. Wu, D. Zaller, X. Zhang, L. Zhu, A.E. Weber, and N.A. Thronberry Diabetes 54 2005 2988
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He, H.10
Ippolito, D.E.11
Kim, D.12
Lyons, K.A.13
Ok, H.O.14
Patel, R.A.15
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Qian, X.18
Reigle, L.19
Woods, A.20
Wu, J.K.21
Zaller, D.22
Zhang, X.23
Zhu, L.24
Weber, A.E.25
Thronberry, N.A.26
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28
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77955387970
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W. Meng, R.P. Brigance, H.J. Chao, A. Fura, T. Harrity, J. Marcinkeviciene, S.P. O'Connor, J.K. Tamura, D. Xie, Y. Zhang, H.E. Klei, K. Kish, C.A. Weigelt, H. Turdi, A. Wang, R. Zahler, M.S. Kirby, and L.G. Hamann J. Med. Chem. 53 2010 5620
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O'Connor, S.P.7
Tamura, J.K.8
Xie, D.9
Zhang, Y.10
Klei, H.E.11
Kish, K.12
Weigelt, C.A.13
Turdi, H.14
Wang, A.15
Zahler, R.16
Kirby, M.S.17
Hamann, L.G.18
-
29
-
-
77957866645
-
-
note
-
R = 11.2 min), 100% ee.
-
-
-
-
30
-
-
77957862206
-
-
note
-
R = 13.1 min), 100% ee.
-
-
-
-
32
-
-
0002999412
-
-
a' stereochemical designation refers to the axis of asymmetry imparted to the molecule by virtue of the restricted rotation around the biaryl bond; see also: M. Oki Top. Stereochem. 14 1984 1
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(1984)
Top. Stereochem.
, vol.14
, pp. 1
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-
Oki, M.1
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