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116
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116
1. Enantiopure drugs
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Stereochemistry
2. Isomerism
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Stereochemistry
3. Racemic mixtures
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Stereochemistry
4. Stereochemistry stubs
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Stereochemistry
5. Stereochemists
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Stereochemistry
6. Absolute configuration
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Stereochemistry
7. Akamptisomer
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Stereochemistry
8. Allylic strain
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Stereochemistry
9. Anomer
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Stereochemistry
10. Antarafacial and suprafacial
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Stereochemistry
11. Asymmetric carbon
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Stereochemistry
12. Asymmetric induction
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Stereochemistry
13. Atropisomer
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Stereochemistry
14. Axial chirality
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Stereochemistry
15. Baldwin's rules
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Stereochemistry
16. Bredt's rule
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Stereochemistry
17. C2-Symmetric ligands
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Stereochemistry
18. Cahn–Ingold–Prelog priority rules
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Stereochemistry
19. Chiral Lewis acid
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Stereochemistry
20. Chiral analysis
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Stereochemistry
21. Chiral auxiliary
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Stereochemistry
22. Chiral column chromatography
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Stereochemistry
23. Chiral derivatizing agent
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Stereochemistry
24. Chiral drugs
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Stereochemistry
25. Chiral inversion
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Stereochemistry
26. Chiral resolution
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Stereochemistry
27. Chiral switch
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Stereochemistry
28. Chiral thin-layer chromatography
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Stereochemistry
29. Chirality
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Stereochemistry
30. Chirality-induced spin selectivity
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Stereochemistry
31. Chirality (chemistry)
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Stereochemistry
32. Chirality timeline
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Stereochemistry
33. Cis–trans isomerism
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Stereochemistry
34. Conformational isomerism
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Stereochemistry
35. Cross-linked enzyme aggregate
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Stereochemistry
36. Cryptochirality
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Stereochemistry
37. Cryptoregiochemistry
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Stereochemistry
38. Cyclohexane conformation
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Stereochemistry
39. Desymmetrization
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Stereochemistry
40. Diastereomer
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Stereochemistry
41. Diastereomeric recrystallization
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Stereochemistry
42. Dynamic kinetic resolution in asymmetric synthesis
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Stereochemistry
43. Dynamic stereochemistry
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Stereochemistry
44. Eclipsed conformation
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Stereochemistry
45. Enantiomer
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Stereochemistry
46. Enantiomer self-disproportionation
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Stereochemistry
47. Enantiomeric excess
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Stereochemistry
48. Enantiopure drug
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Stereochemistry
49. Enantioselective synthesis
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Stereochemistry
50. Endo-exo isomerism
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Stereochemistry
51. Epimer
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Stereochemistry
52. Eudysmic ratio
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Stereochemistry
53. E–Z notation
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Stereochemistry
54. Fischer projection
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Stereochemistry
55. Fuzzy complex
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Stereochemistry
56. Fürst-Plattner Rule
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Stereochemistry
57. Gauche effect
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Stereochemistry
58. Haworth projection
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Stereochemistry
59. Hexol
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Stereochemistry
60. Homochirality
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Stereochemistry
61. Homometric structures
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Stereochemistry
62. Immobilized enzyme
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Stereochemistry
63. Inherent chirality
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Stereochemistry
64. Kinetic resolution
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Stereochemistry
65. Klyne–Prelog system
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Stereochemistry
66. Kryptoracemic compounds
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Stereochemistry
67. Le Bel–Van 't Hoff rule
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Stereochemistry
68. Ligand cone angle
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Stereochemistry
69. Meso compound
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Stereochemistry
70. Molecular configuration
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Stereochemistry
71. Mosher's acid
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Stereochemistry
72. Mutarotation
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Stereochemistry
73. Natta projection
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Stereochemistry
74. Newman projection
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Stereochemistry
75. Noyori asymmetric hydrogenation
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Stereochemistry
76. Optical rotation
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Stereochemistry
77. Optical rotatory dispersion
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Stereochemistry
78. P-Chiral phosphine
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Stereochemistry
79. Pentane interference
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Stereochemistry
80. Pfeiffer effect
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Stereochemistry
81. Pirkle's alcohol
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Stereochemistry
82. Planar chirality
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Stereochemistry
83. Prelog strain
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Stereochemistry
84. Prochirality
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Stereochemistry
85. Proline isomerization in epigenetics
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Stereochemistry
86. Protein primary structure
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Stereochemistry
87. Protein quaternary structure
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Stereochemistry
88. Protein secondary structure
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Stereochemistry
89. Pseudorotation
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Stereochemistry
90. Pyramidal inversion
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Stereochemistry
91. Racemic acid
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Stereochemistry
92. Racemic mixture
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Stereochemistry
93. Racemization
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Stereochemistry
94. Regioselectivity
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Stereochemistry
95. Serine octamer cluster
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Stereochemistry
96. Soai reaction
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Stereochemistry
97. Specific rotation
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Stereochemistry
98. Spontaneous absolute asymmetric synthesis
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Stereochemistry
99. Staggered conformation
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Stereochemistry
100. Stereocenter
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Stereochemistry
101. Stereoelectronic effect
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Stereochemistry
102. Stereoisomerism
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Stereochemistry
103. Stereoselectivity
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Stereochemistry
104. Stereospecificity
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Stereochemistry
105. Steric effects
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Stereochemistry
106. Sterimol parameter
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Stereochemistry
107. Strain (chemistry)
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Stereochemistry
108. Supramolecular chirality
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Stereochemistry
109. Syn and anti addition
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Stereochemistry
110. Tacticity
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Stereochemistry
111. Thorpe–Ingold effect
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Stereochemistry
112. Topicity
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Stereochemistry
113. Topoisomer
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Stereochemistry
114. Torquoselectivity
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Stereochemistry
115. Van der Waals strain
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Stereochemistry
116. Viedma ripening
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Stereochemistry
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