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Cambridge Crystallographic Data Centre: Cambridge, UK, November update
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Cambridge Structural Database, Version 5.24; Cambridge Crystallographic Data Centre: Cambridge, UK, November 2002 update.
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34
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0003591868
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Bruker AXS, Inc.: Madison, Wisconsin
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SMART, Version 5.05; Bruker AXS, Inc.: Madison, Wisconsin, 1998.
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35
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0004022783
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Bruker AXS, Inc.: Madison, Wisconsin
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SAINT, Version 6.2, Bruker AXS, Inc.: Madison, Wisconsin, 2001.
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SAINT, Version 6.2
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37
-
-
0344756921
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-
note
-
The crystal structure of the EtOH-water solvate will be disclosed in a separate report.
-
-
-
-
40
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-
0003422019
-
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Wavefunction, Inc.: Irvine, CA
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Spartan, Version 5.0; Wavefunction, Inc.: Irvine, CA, 1992.
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Spartan, Version 5.0
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41
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37049105897
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Rapid interconversion of diazepine ring conformers has also been observed in the structurally related dibenzodiazepine, clozapine and is attributed to the low activation energy for inversion. Petcher, T. J.; Weber, H.-P. J. Chem. Soc., Perkin Trans. 2 1976, 1415-1420.
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Petcher, T.J.1
Weber, H.-P.2
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42
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0344324773
-
-
note
-
2 hemisolvate), for which X-ray structures have been determined, each feature the olanzapine dimer.
-
-
-
-
43
-
-
0345187264
-
-
note
-
Refcodes for retrieved structures: CIJMIR, HIFRET, NDNCLH01, NDNHCL01, NDNHCL10, and YUYMUA.
-
-
-
-
44
-
-
0345619354
-
-
note
-
The energetically equivalent mirror image of conformer A was also obtained.
-
-
-
-
45
-
-
0026600109
-
-
Analysis of hydrogen-bonding patterns in small peptides has previously revealed that water most frequently donates two hydrogen bonds and accepts one. The criteria for hydrogen bonding outlined by Görbitz and Etter were used to establish the hydrogen-bonding topology in the olanzapine dihydrates. Görbitz, C. H.; Etter, M. C. Int. J. Peptide Protein Res. 1992, 39, 93-110.
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Görbitz, C.H.1
Etter, M.C.2
-
46
-
-
0344756920
-
-
note
-
Because the water hydrogens were not located in the crystal structure determinations, nonbonded contacts to the waters of crystallization were identified by carefully examining heavy atom distances, with consideration given to hydrogen-bond angles.
-
-
-
-
49
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0028168289
-
-
15N resonance will shift to higher or lower frequencies, respectively. Naito, A.; Tuzi, S.; Saito, H. Eur. J. Biochem. 1994, 224, 729-734.
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Naito, A.1
Tuzi, S.2
Saito, H.3
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0029070763
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Hoiberg, C.4
Poochikian, G.5
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53
-
-
0344324772
-
-
note
-
3, respectively, were calculated.
-
-
-
-
55
-
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0000201963
-
-
Lommerse, J. P. M.; Motherwell, W. D. S.; Amon, H. L.; Dunitz, J. D.; Gavezzotti, A.; Hofmann, D. W. M.; Leusen, F. J. J.; Mooij, W. T. M.; Price, S. L.; Schweizer, B.; Schmidt, M. U.; van Eijck, B. P.; Verwer, P.; Williams, D. E. Acta Cryst. 2000, B56, 697-714.
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Lommerse, J.P.M.1
Motherwell, W.D.S.2
Amon, H.L.3
Dunitz, J.D.4
Gavezzotti, A.5
Hofmann, D.W.M.6
Leusen, F.J.J.7
Mooij, W.T.M.8
Price, S.L.9
Schweizer, B.10
Schmidt, M.U.11
Van Eijck, B.P.12
Verwer, P.13
Williams, D.E.14
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56
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0344756919
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note
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There are numerous examples of highly studied pharmaceutical compounds (aspirin (ACSALA01), ibuprofen (IBPRAC), and fluoxetine HCl (FUDCOW) - the active ingredient in Prozac, to name a few) that, to date, are monomorphic.
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