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1 1,3-Dipolar cycloaddition (t · h · l) Mid 2009-03-02 (t C 2011-12-23 (t 903
2 2+2 Photocycloaddition (t · h · l) Mid 2010-12-23 (t C 2010-12-23 (t 526
3 2,3-Wittig rearrangement (t · h · l) Mid 2010-12-23 (t C 2010-12-23 (t 526
4 2-Norbornyl cation (t · h · l) Mid 2009-03-07 (t C 2009-03-07 (t 526
5 4+3 cycloaddition (t · h · l) Mid 2010-12-23 (t C 2010-12-23 (t 526
6 ACS Chemical Biology (t · h · l) Mid 2009-01-13 (t C 2009-01-13 (t 706
7 Ab initio quantum chemistry methods (t · h · l) Mid 2013-07-24 (t C 2013-07-24 (t 996
8 Absorption spectroscopy (t · h · l) Mid 2010-02-21 (t C 2010-02-21 (t 1202
9 Acid-base extraction (t · h · l) Mid 2009-06-23 (t C 2009-02-28 (t 883
10 Activated carbon (t · h · l) Mid 2010-12-19 (t C 2010-12-19 (t 1290
11 Activity coefficient (t · h · l) Mid 2009-01-09 (t C 2009-06-25 (t 914
12 Acyloin (t · h · l) Mid 2009-05-13 (t C 2009-05-13 (t 887
13 Ada Hitchins (t · h · l) Mid 2014-04-15 (t C 2014-04-15 (t 526
14 Ada Yonath (t · h · l) Mid 2013-04-13 (t C 2012-11-02 (t 1200
15 Adhesive (t · h · l) Mid 2009-04-13 (t C 2009-04-13 (t 1347
16 Aerosol (t · h · l) Mid 2013-04-13 (t C 2012-09-15 (t 1299
17 Air-free technique (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 827
18 Alchemy and chemistry in medieval Islam (t · h · l) Mid 2012-02-15 (t C 2012-02-15 (t 964
19 Aldol condensation (t · h · l) Mid 2009-02-28 (t C 2009-02-28 (t 1028
20 Alexandra Navrotsky (t · h · l) Mid 2010-02-12 (t C 2010-02-12 (t 597
21 Alkaline battery (t · h · l) Mid 2009-10-16 (t C 2011-02-10 (t 1157
22 Alkoxide (t · h · l) Mid 2009-04-13 (t C 2009-04-13 (t 1128
23 Alkylimino-de-oxo-bisubstitution (t · h · l) Mid 2009-01-09 (t C 2009-01-09 (t 718
24 Alkyne metathesis (t · h · l) Mid 2009-02-28 (t C 2009-02-28 (t 660
25 Alkyne trimerisation (t · h · l) Mid 2009-02-28 (t C 2009-02-28 (t 702
26 Allotropes of carbon (t · h · l) Mid 2009-01-09 (t C 2011-02-26 (t 1002
27 Allotropes of oxygen (t · h · l) Mid 2009-04-12 (t C 2010-10-19 (t 826
28 Allylic rearrangement (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 792
29 Alpha decay (t · h · l) Mid 2009-04-12 (t C 2009-02-21 (t 1291
30 Amedeo Avogadro (t · h · l) Mid 2013-06-15 (t C 2013-06-15 (t 1286
31 American Chemical Society (t · h · l) Mid 2009-01-11 (t C 2010-01-18 (t 1211
32 Andreas Sigismund Marggraf (t · h · l) Mid 2009-06-14 (t C 2010-01-23 (t 957
33 Angewandte Chemie (t · h · l) Mid 2009-01-09 (t C 2009-09-09 (t 1077
34 Angle strain (t · h · l) Mid 2009-03-02 (t C 2011-06-19 (t 803
35 Aqua regia (t · h · l) Mid 2009-03-26 (t C 2009-02-28 (t 1267
36 Aromatic ring current (t · h · l) Mid 2009-03-02 (t C 2009-03-02 (t 728
37 Arrow poison (t · h · l) Mid 2009-03-03 (t C 2009-03-03 (t 924
38 Arsenic toxicity (t · h · l) Mid 2009-04-28 (t C 2009-02-28 (t 648
39 Aryl halide (t · h · l) Mid 2013-12-27 (t C 2013-12-27 (t 526
40 Aryne (t · h · l) Mid 2009-05-11 (t C 2009-05-11 (t 920
41 Association of Applied Geochemists (t · h · l) Mid 2010-09-14 (t C 2010-09-14 (t 610
42 Asymmetric nucleophilic epoxidation (t · h · l) Mid 2011-01-04 (t C 2011-01-04 (t 526
43 Atmospheric carbon cycle (t · h · l) Mid 2013-09-23 (t C 2013-09-23 (t 526
44 Atropisomer (t · h · l) Mid 2009-01-28 (t C 2009-01-28 (t 834
45 Azide-alkyne Huisgen cycloaddition (t · h · l) Mid 2009-02-28 (t C 2009-02-28 (t 526
46 Azimuthal quantum number (t · h · l) Mid 2011-02-25 (t C 2011-02-25 (t 1097
47 Barton–McCombie deoxygenation (t · h · l) Mid 2009-06-22 (t C 2009-06-22 (t 845
48 Basis set (chemistry) (t · h · l) Mid 2011-01-07 (t C 2014-01-17 (t 969
49 Battery (electricity) (t · h · l) Mid 2013-04-13 (t C 2013-04-13 (t 1429
50 Bauxite (t · h · l) Mid 2009-10-21 (t C 2009-10-21 (t 1349
51 Baylis–Hillman reaction (t · h · l) Mid 2009-06-21 (t C 2009-06-21 (t 962
52 Bent bond (t · h · l) Mid 2009-01-11 (t C 2009-01-11 (t 961
53 Benzilic acid rearrangement (t · h · l) Mid 2009-03-02 (t C 2009-02-28 (t 761
54 Benzyl (t · h · l) Mid 2009-03-02 (t C 2009-01-09 (t 1097
55 Beta-Hydride elimination (t · h · l) Mid 2009-05-28 (t C 2009-05-28 (t 831
56 Binodal (t · h · l) Mid 2012-08-23 (t C 2012-08-23 (t 874
57 Biomonitoring (t · h · l) Mid 2011-01-07 (t C 2011-01-07 (t 954
58 Bisulfite (t · h · l) Mid 2009-03-02 (t C 2009-01-09 (t 918
59 Bite angle (t · h · l) Mid 2009-03-02 (t C 2009-03-02 (t 673
60 Boiling-point elevation (t · h · l) Mid 2011-02-25 (t C 2011-02-25 (t 1051
61 Boranes (t · h · l) Mid 2009-03-02 (t C 2009-03-02 (t 526
62 Borderline hydrides (t · h · l) Mid 2011-01-07 (t C 2011-01-07 (t 541
63 Borohydride (t · h · l) Mid 2012-05-18 (t C 2013-09-24 (t 694
64 Boudouard reaction (t · h · l) Mid 2009-03-01 (t C 2013-09-14 (t 898
65 Brass (t · h · l) Mid 2011-03-04 (t C 2011-03-04 (t 1448
66 Briggs–Rauscher reaction (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 876
67 Bronze (t · h · l) Mid 2011-03-04 (t C 2011-03-04 (t 1499
68 Buchwald–Hartwig amination (t · h · l) Mid 2009-06-22 (t C 2009-06-22 (t 897
69 Bunsen burner (t · h · l) Mid 2010-12-22 (t C 2010-12-22 (t 1227
70 Calorimeter (t · h · l) Mid 2011-09-20 (t C 2011-09-20 (t 1251
71 Carbanion (t · h · l) Mid 2009-05-11 (t C 2009-05-11 (t 1115
72 Carbide (t · h · l) Mid 2009-04-14 (t C 2009-04-14 (t 1204
73 Carbocation (t · h · l) Mid 2009-05-11 (t C 2009-05-11 (t 1148
74 Carbohydrate synthesis (t · h · l) Mid 2011-02-16 (t C 2011-02-16 (t 681
75 Carbometalation (t · h · l) Mid 2009-03-02 (t C 2009-03-02 (t 724
76 Carbon black (t · h · l) Mid 2009-06-21 (t C 2009-06-21 (t 1149
77 Carbon nanocone (t · h · l) Mid 2011-02-16 (t C 2011-02-16 (t 643
78 Carbon sequestration (t · h · l) Mid 2009-04-13 (t C 2009-04-13 (t 1114
79 Carbonyl oxidation with hypervalent iodine reagents (t · h · l) Mid 2011-10-08 (t C 2011-10-08 (t 526
80 Carbonyl reduction (t · h · l) Mid 2010-12-20 (t C 2010-12-20 (t 684
81 Carbonylation (t · h · l) Mid 2009-03-12 (t C 2009-03-12 (t 986
82 Carbon–fluorine bond (t · h · l) Mid 2009-03-12 (t C 2009-03-12 (t 875
83 Carbon–hydrogen bond activation (t · h · l) Mid 2009-04-15 (t C 2009-04-15 (t 526
84 Carcerand (t · h · l) Mid 2009-06-07 (t C 2009-06-07 (t 660
85 Carnot heat engine (t · h · l) Mid 2009-01-09 (t C 2009-01-09 (t 1074
86 Cascade reaction (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 866
87 Castner–Kellner process (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 526
88 Catalytic reforming (t · h · l) Mid 2009-06-06 (t C 2009-06-06 (t 1064
89 Cationic polymerization (t · h · l) Mid 2011-04-11 (t C 2011-04-11 (t 745
90 Charge-transfer complex (t · h · l) Mid 2009-12-06 (t C 2009-12-06 (t 914
91 Cheletropic reaction (t · h · l) Mid 2011-02-18 (t C 2011-02-18 (t 822
92 Chemical oxygen demand (t · h · l) Mid 2013-04-16 (t C 2013-04-16 (t 1136
93 Chemical potential (t · h · l) Mid 2010-08-13 (t C 2010-08-13 (t 1203
94 Chemical warfare (t · h · l) Mid 2009-03-04 (t C 2009-03-22 (t 1404
95 Chemical weapon (t · h · l) Mid 2010-09-19 (t C 2013-08-27 (t 526
96 Chiral Lewis acid (t · h · l) Mid 2011-04-28 (t C 2011-04-28 (t 651
97 Chiral ligand (t · h · l) Mid 2009-05-14 (t C 2009-05-14 (t 756
98 Chiral resolution (t · h · l) Mid 2009-03-07 (t C 2009-03-07 (t 901
99 Chlorine production (t · h · l) Mid 2009-04-12 (t C 2009-01-13 (t 624
100 Cholesterol total synthesis (t · h · l) Mid 2011-10-07 (t C 2011-10-07 (t 526
101 Chromate and dichromate (t · h · l) Mid 2009-11-03 (t C 2009-11-03 (t 1142
102 Chrome plating (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 1109
103 Citrate (t · h · l) Mid 2009-03-20 (t C 2009-03-20 (t 1153
104 Classical element (t · h · l) Mid 2009-04-16 (t C 2009-01-09 (t 1325
105 Cluster chemistry (t · h · l) Mid 2010-12-19 (t C 2010-12-19 (t 1045
106 Coal tar (t · h · l) Mid 2014-01-27 (t C 2014-01-27 (t 1149
107 Colloidal gold (t · h · l) Mid 2009-03-23 (t C 2009-01-13 (t 990
108 Colored gold (t · h · l) Mid 2011-01-13 (t C 2011-01-13 (t 1239
109 Combustion analysis (t · h · l) Mid 2009-06-03 (t C 2009-06-03 (t 663
110 Conjugated system (t · h · l) Mid 2009-01-09 (t C 2009-01-09 (t 1158
111 Cool flame (t · h · l) Mid 2011-05-04 (t C 2011-05-04 (t 621
112 Coordination polymer (t · h · l) Mid 2011-01-06 (t C 2011-01-06 (t 526
113 Cope rearrangement (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 915
114 Corey–Itsuno reduction (t · h · l) Mid 2011-04-02 (t C 2011-04-02 (t 526
115 Coulometry (t · h · l) Mid 2009-01-10 (t C 2009-01-10 (t 946
116 Cryptand (t · h · l) Mid 2014-03-26 (t C 2014-03-26 (t 950
117 Crystal growth (t · h · l) Mid 2014-06-02 (t C 2014-06-02 (t 823
118 Cubic crystal system (t · h · l) Mid 2012-01-08 (t C 2014-03-27 (t 1243
119 Cumene process (t · h · l) Mid 2009-03-14 (t C 2009-03-14 (t 948
120 Cuprate (t · h · l) Mid 2013-10-13 (t C 2013-10-13 (t 878
121 Curcuminoid (t · h · l) Mid 2011-02-16 (t C 2011-02-16 (t 649
122 Curtin–Hammett principle (t · h · l) Mid 2009-01-09 (t C 2009-01-09 (t 700
123 Cyanoacrylate (t · h · l) Mid 2009-03-12 (t C 2009-03-12 (t 1162
124 Cyclic voltammetry (t · h · l) Mid 2009-01-09 (t C 2009-01-09 (t 1003
125 Cyclohexane conformation (t · h · l) Mid 2009-05-14 (t C 2009-05-14 (t 1110
126 Cyclophane (t · h · l) Mid 2011-02-16 (t C 2011-02-16 (t 962
127 Cyclopropanation (t · h · l) Mid 2013-04-01 (t C 2013-04-01 (t 526
128 Cyclopropane (t · h · l) Mid 2011-08-28 (t C 2011-08-28 (t 1212
129 Cytochrome c oxidase (t · h · l) Mid 2010-09-17 (t C 2010-09-17 (t 1136
130 Dean-Stark apparatus (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 924
131 Debye–Hückel theory (t · h · l) Mid 2012-01-07 (t C 2010-12-17 (t 526
132 Decarboxylation (t · h · l) Mid 2009-03-04 (t C 2009-03-04 (t 1148
133 Deformulation (t · h · l) Mid 2012-01-09 (t C 2012-01-09 (t 526
134 Desiccant (t · h · l) Mid 2013-08-15 (t C 2013-08-15 (t 1131
135 Detailed balance (t · h · l) Mid 2012-06-23 (t C 2012-06-23 (t 847
136 Detection limit (t · h · l) Mid 2009-04-13 (t C 2009-04-13 (t 945
137 Determination of equilibrium constants (t · h · l) Mid 2014-02-14 (t C 2014-02-14 (t 718
138 Diazonium compound (t · h · l) Mid 2009-05-13 (t C 2009-05-13 (t 1115
139 Dihydrogen complex (t · h · l) Mid 2009-06-23 (t C 2009-01-11 (t 759
140 Disulfide (t · h · l) Mid 2009-01-09 (t C 2009-01-09 (t 1046
141 Drug design (t · h · l) Mid 2009-04-21 (t C 2009-04-21 (t 1018
142 DuPont Central Research (t · h · l) Mid 2012-04-15 (t C 2012-04-15 (t 765
143 Dynamic mechanical analysis (t · h · l) Mid 2011-05-06 (t C 2011-05-06 (t 944
144 Edward Schunck (t · h · l) Mid 2009-06-13 (t C 2009-06-13 (t 640
145 Edward Weston (chemist) (t · h · l) Mid 2011-12-19 (t C 2011-12-19 (t 818
146 Eilhard Mitscherlich (t · h · l) Mid 2009-06-14 (t C 2009-06-14 (t 973
147 Elbs reaction (t · h · l) Mid 2009-03-14 (t C 2009-03-14 (t 781
148 Electrolysis of water (t · h · l) Mid 2009-06-04 (t C 2009-06-04 (t 1102
149 Electrolyte (t · h · l) Mid 2010-09-17 (t C 2009-01-13 (t 1391
150 Electron paramagnetic resonance (t · h · l) Mid 2010-12-22 (t C 2010-12-22 (t 1210
151 Electrophilic amination (t · h · l) Mid 2011-04-10 (t C 2011-04-10 (t 526
152 Electrophilic halogenation (t · h · l) Mid 2009-04-12 (t C 2009-04-12 (t 857
153 Electrosynthesis (t · h · l) Mid 2009-03-07 (t C 2009-03-07 (t 811
154 Ene reaction (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 859
155 Energy profile (chemistry) (t · h · l) Mid 2011-11-19 (t C 2013-11-14 (t 603
156 Enyne metathesis (t · h · l) Mid 2009-03-07 (t C 2009-03-07 (t 718
157 Fatty alcohol (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 1009
158 Fehling's solution (t · h · l) Mid 2009-03-04 (t C 2009-03-04 (t 1085
159 Ferrate(VI) (t · h · l) Mid 2013-11-16 (t C 2013-11-16 (t 526
160 Ferrocyanide (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 818
161 Force field (chemistry) (t · h · l) Mid 2013-07-06 (t C 2013-07-06 (t 981
162 Fowler process (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 610
163 Fractional distillation (t · h · l) Mid 2009-06-04 (t C 2009-06-04 (t 1211
164 Free-radical addition (t · h · l) Mid 2009-05-11 (t C 2009-05-11 (t 526
165 Free-radical halogenation (t · h · l) Mid 2011-09-18 (t C 2011-09-18 (t 526
166 Freezing-point depression (t · h · l) Mid 2010-02-15 (t C 2009-11-03 (t 1101
167 Fries rearrangement (t · h · l) Mid 2009-03-14 (t C 2009-03-14 (t 837
168 Frost flower (sea ice) (t · h · l) Mid 2010-04-06 (t C 2010-04-06 (t 606
169 Galactomannan (t · h · l) Mid 2009-01-08 (t C 2009-01-08 (t 986
170 Gallium halides (t · h · l) Mid 2009-03-03 (t C 2009-03-03 (t 591
171 Galvanic cell (t · h · l) Mid 2009-01-13 (t C 2009-01-13 (t 1222
172 Galvanic corrosion (t · h · l) Mid 2011-01-19 (t C 2011-01-19 (t 1052
173 Gamma spectroscopy (t · h · l) Mid 2009-01-08 (t C 2010-11-12 (t 930
174 Gel (t · h · l) Mid 2010-12-18 (t C 2010-12-18 (t 1292
175 Georgius Agricola (t · h · l) Mid 2009-06-25 (t C 2009-06-25 (t 1200
176 Glassy carbon (t · h · l) Mid 2009-06-23 (t C 2009-01-09 (t 911
177 Glycosidic bond (t · h · l) Mid 2009-05-13 (t C 2009-05-13 (t 1167
178 Gustavus Detlef Hinrichs (t · h · l) Mid 2009-11-03 (t C 2009-11-10 (t 560
179 Hajos–Parrish–Eder–Sauer–Wiechert reaction (t · h · l) Mid 2009-11-03 (t C 2009-11-03 (t 803
180 Hall–Héroult process (t · h · l) Mid 2009-06-04 (t C 2009-06-04 (t 1077
181 Halogenated ether (t · h · l) Mid 2009-03-03 (t C 2009-03-03 (t 852
182 Halomethane (t · h · l) Mid 2013-10-31 (t C 2013-10-31 (t 985
183 Hemiacetal (t · h · l) Mid 2009-04-11 (t C 2009-04-11 (t 1062
184 Henderson–Hasselbalch equation (t · h · l) Mid 2009-01-09 (t C 2014-02-08 (t 1124
185 Henry Louis Le Chatelier (t · h · l) Mid 2014-01-27 (t C 2014-01-27 (t 1114
186 Hermann Emil Fischer (t · h · l) Mid 2009-06-13 (t C 2009-06-13 (t 1248
187 Heterocyclic amine (t · h · l) Mid 2013-10-24 (t C 2013-10-24 (t 898
188 Hexafluoride (t · h · l) Mid 2009-01-08 (t C 2009-01-08 (t 691
189 Hexavalent chromium (t · h · l) Mid 2013-07-25 (t C 2013-07-25 (t 981
190 History of mineralogy (t · h · l) Mid 2012-03-12 (t C 2012-03-12 (t 595
191 Homoaromaticity (t · h · l) Mid 2011-10-11 (t C 2011-10-11 (t 694
192 Host–guest chemistry (t · h · l) Mid 2013-06-15 (t C 2013-06-15 (t 526
193 Hydride (t · h · l) Mid 2009-12-23 (t C 2013-10-24 (t 1236
194 Hydrocyanation of unsaturated carbonyl compounds (t · h · l) Mid 2011-06-13 (t C 2011-06-13 (t 526
195 Hydroformylation (t · h · l) Mid 2009-03-23 (t C 2009-03-23 (t 1050
196 Hydrophobe (t · h · l) Mid 2009-01-09 (t C 2009-01-09 (t 1249
197 Hypervalent molecule (t · h · l) Mid 2013-10-04 (t C 2013-10-04 (t 976
198 IUPAC nomenclature of inorganic chemistry 2005 (t · h · l) Mid 2009-07-14 (t C 2009-07-14 (t 696
199 IUPAC numerical multiplier (t · h · l) Mid 2014-02-19 (t C 2014-01-27 (t 709
200 Ice (t · h · l) Mid 2013-06-06 (t C 2013-06-06 (t 1474
201 Imine (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 1186
202 Indium chalcogenides (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 666
203 Insertion reaction (t · h · l) Mid 2014-03-28 (t C 2014-03-28 (t 655
204 Intermolecular metal-catalyzed carbenoid cyclopropanations (t · h · l) Mid 2013-01-07 (t C 2013-01-07 (t 526
205 Intramolecular Heck reaction (t · h · l) Mid 2011-10-07 (t C 2011-10-07 (t 526
206 Inverse electron-demand Diels–Alder reaction (t · h · l) Mid 2013-05-03 (t C 2013-05-03 (t 526
207 Iodine clock reaction (t · h · l) Mid 2009-03-02 (t C 2009-03-02 (t 823
208 Iodolactonization (t · h · l) Mid 2013-04-15 (t C 2013-04-15 (t 526
209 Ion-exchange resin (t · h · l) Mid 2010-05-13 (t C 2010-05-13 (t 1107
210 Ion exchange (t · h · l) Mid 2009-06-03 (t C 2009-06-03 (t 1168
211 Ionic compound (t · h · l) Mid 2009-04-11 (t C 2009-04-11 (t 1077
212 Ionic radius (t · h · l) Mid 2009-04-11 (t C 2009-04-11 (t 1124
213 Isoflavones (t · h · l) Mid 2009-04-25 (t C 2009-04-25 (t 1084
214 Isomeric shift (t · h · l) Mid 2009-04-12 (t C 2009-04-08 (t 677
215 Isotope dilution (t · h · l) Mid 2014-02-07 (t C 2014-02-07 (t 526
216 Isotopic labeling (t · h · l) Mid 2011-01-07 (t C 2011-01-07 (t 1009
217 Jerome Karle (t · h · l) Mid 2014-01-17 (t C 2010-08-09 (t 1132
218 John A. Quinn (t · h · l) Mid 2012-11-17 (t C 2012-11-17 (t 526
219 John C. Sheehan (t · h · l) Mid 2013-01-26 (t C 2013-01-26 (t 661
220 Jones oxidation (t · h · l) Mid 2011-04-23 (t C 2011-04-23 (t 967
221 Julia olefination (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 812
222 Julius Lothar Meyer (t · h · l) Mid 2009-06-14 (t C 2009-06-14 (t 1092
223 Karlsruhe Congress (t · h · l) Mid 2009-01-09 (t C 2010-08-20 (t 807
224 Keggin structure (t · h · l) Mid 2013-07-18 (t C 2013-07-18 (t 711
225 Keto–enol tautomerism (t · h · l) Mid 2013-05-25 (t C 2013-05-25 (t 526
226 Kiliani–Fischer synthesis (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 526
227 Kinetic resolution (t · h · l) Mid 2009-01-28 (t C 2009-01-28 (t 763
228 Knoevenagel condensation (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 1012
229 Kulinkovich reaction (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 761
230 Laboratory glassware (t · h · l) Mid 2009-04-13 (t C 2009-04-13 (t 1137
231 Laboratory information management system (t · h · l) Mid 2013-10-18 (t C 2013-10-18 (t 1010
232 Lactone (t · h · l) Mid 2009-04-13 (t C 2009-04-13 (t 1175
233 Langmuir adsorption model (t · h · l) Mid 2009-04-11 (t C 2009-04-11 (t 625
234 Lanthanide contraction (t · h · l) Mid 2009-03-03 (t C 2009-03-03 (t 932
235 Lanthanide trifluoromethanesulfonates (t · h · l) Mid 2009-05-14 (t C 2009-05-14 (t 612
236 Lead chamber process (t · h · l) Mid 2009-02-18 (t C 2009-02-18 (t 918
237 Lead–acid battery (t · h · l) Mid 2010-03-17 (t C 2010-03-17 (t 1274
238 Liquid–liquid extraction (t · h · l) Mid 2009-04-13 (t C 2009-04-13 (t 526
239 Lonsdaleite (t · h · l) Mid 2009-04-13 (t C 2012-12-30 (t 1060
240 Macrocycle (t · h · l) Mid 2009-04-13 (t C 2009-04-13 (t 993
241 Mannich reaction (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 1004
242 Marcus theory (t · h · l) Mid 2011-11-14 (t C 2011-11-14 (t 835
243 Match (t · h · l) Mid 2009-01-13 (t C 2009-01-13 (t 1368
244 Max Bodenstein (t · h · l) Mid 2009-06-13 (t C 2009-06-13 (t 857
245 McMurry reaction (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 854
246 Mechanistic organic photochemistry (t · h · l) Mid 2011-04-24 (t C 2011-04-24 (t 526
247 Meisenheimer complex (t · h · l) Mid 2009-03-01 (t C 2009-03-01 (t 703
248 Mesoporous silica (t · h · l) Mid 2009-01-11 (t C 2013-12-02 (t 676
249 Metal-catalysed hydroboration (t · h · l) Mid 2014-03-12 (t C 2014-03-12 (t 526
250 Metal acetylacetonates (t · h · l) Mid 2011-03-03 (t C 2011-03-03 (t 526
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