User contributions for Tna08

4 March 2011

• 14:1514:15, 4 March 2011 diff hist +477 Mod.timarbab →Stereochemistry and Reactivity of an Intermediate in the Synthesis of Taxol
• 02:4902:49, 4 March 2011 diff hist +384 Mod.timarbab →Stereochemistry and Reactivity of an Intermediate in the Synthesis of Taxol
• 02:4602:46, 4 March 2011 diff hist +695 Mod.timarbab →Stereochemistry and Reactivity of an Intermediate in the Synthesis of Taxol
• 02:4502:45, 4 March 2011 diff hist +11 N File:10 mol.mol Jmol for 10
• 02:4502:45, 4 March 2011 diff hist +10 N File:9 mol.mol Jmol for 9
• 02:4402:44, 4 March 2011 diff hist +1 Mod.timarbab →Stereochemistry and Reactivity of an Intermediate in the Synthesis of Taxol
• 02:4402:44, 4 March 2011 diff hist +38 N File:Picture 9 atropisomers 9 and 102.jpg Fig. 9: The two atropisomers 9 and 10. current
• 02:4102:41, 4 March 2011 diff hist +1 Mod.timarbab →Stereochemistry and Reactivity of an Intermediate in the Synthesis of Taxol
• 02:4102:41, 4 March 2011 diff hist +109 N File:Picture 10 9 and 10 energy table2.jpg Fig. 10: The Total Energy achieved for the two atropisomers, 9 and 10, when using two different force fields. current
• 02:3902:39, 4 March 2011 diff hist +465 Mod.timarbab →Stereochemistry and Reactivity of an Intermediate in the Synthesis of Taxol
• 02:3902:39, 4 March 2011 diff hist +109 N File:Picture 10 9 and 10 energy table.jpg Fig. 10: The Total Energy achieved for the two atropisomers, 9 and 10, when using two different force fields. current
• 02:2202:22, 4 March 2011 diff hist +14 Mod.timarbab →Modelling Using Semi-Emperical Molecular Orbital Theory
• 02:1102:11, 4 March 2011 diff hist 0 Mod.timarbab →References
• 02:1002:10, 4 March 2011 diff hist +347 Mod.timarbab →Modelling Using Molecular Mechanics
• 02:1002:10, 4 March 2011 diff hist +38 N File:Picture 9 atropisomers 9 and 10.jpg Fig. 9: The two atropisomers 9 and 10. current
• 02:0302:03, 4 March 2011 diff hist +28 Mod.timarbab →Modelling Using Molecular Mechanics
• 01:4801:48, 4 March 2011 diff hist +1,199 Mod.timarbab →Nucleophilic addition of NHPhenyl group to a pyridinium ring
• 01:4601:46, 4 March 2011 diff hist +9 N File:8 mol.mol Jmol of 8 current
• 01:4601:46, 4 March 2011 diff hist +9 N File:7 mol.mol Jmol of 7 current
• 01:4501:45, 4 March 2011 diff hist +9 N File:6 mol.mol Jmol of 6 current
• 01:4401:44, 4 March 2011 diff hist +10 N File:5 final versionmol.mol Jmol for 5 current
• 01:3701:37, 4 March 2011 diff hist +657 Mod.timarbab →Nucleophilic addition of NHPhenyl group to a pyridinium ring
• 01:3101:31, 4 March 2011 diff hist +52 N File:Picture 7 Mechanism of 7version2.jpg Fig. 7: Mechanism for the reaction of 7 to become 8. current
• 01:2401:24, 4 March 2011 diff hist +167 Mod.timarbab →Stereochemistry of Nucleophilic Additions to a Pyridinium Ring
• 01:2301:23, 4 March 2011 diff hist −25 Mod.timarbab →Reaction of prolinol with MgMeI
• 01:2201:22, 4 March 2011 diff hist +65 Mod.timarbab →Reaction of prolinol with MgMeI
• 01:2101:21, 4 March 2011 diff hist +52 N File:Picture 7 Mechanism of 7.jpg Fig. 7: Mechanism for the reaction of 7 to become 8. current
• 01:2001:20, 4 March 2011 diff hist +54 N File:Picture 6 Mechanism of 5.jpg Fig. 6: The mechanism of prolinol reacting with MgMeI. current
• 01:1501:15, 4 March 2011 diff hist +561 Mod.timarbab →Stereochemistry of Nucleophilic Additions to a Pyridinium Ring

3 March 2011

• 23:3123:31, 3 March 2011 diff hist +7 Mod.timarbab →The Hydrogenation of Cyclopentadiene
• 23:3023:30, 3 March 2011 diff hist +125 N File:Picture 5 molecules 3 and 4.jpg Fig. 5: The 2-D and 3-D representations of the molecules 3 and 4. As with the tables, 3 is on the left and 4 is on the right. current
• 23:2923:29, 3 March 2011 diff hist +144 N File:Picture 4 tables for 3 and 4.jpg Fig. 4: The tables showing the information produced by the energy minimisation. On the left is the product 3 and on the right is the product 4. current
• 23:2823:28, 3 March 2011 diff hist +11 Mod.timarbab →Dimerisation of cyclopentadiene
• 23:2723:27, 3 March 2011 diff hist +146 N File:Picture 3 molecules 1 and 2timarbab.jpg Fig. 3: The 2-D and 3-D representations, created by ChemBio 3D Ultra 12, after the MM2 optimisation. Exo (1) form is on the left and the endo (2). current
• 22:3722:37, 3 March 2011 diff hist +323 Mod.timarbab →Dimerisation of cyclopentadiene
• 22:3122:31, 3 March 2011 diff hist +2,788 Mod.timarbab →The Hydrogenation of Cyclopentadiene
• 22:2822:28, 3 March 2011 diff hist +1,391 Mod.timarbab →The Hydrogenation of Cyclopentadiene
• 22:2322:23, 3 March 2011 diff hist +290 Mod.timarbab →The Hydrogenation of Cyclopentadiene
• 22:2122:21, 3 March 2011 diff hist +112 N File:Picture 2 tables for 1 2.jpg Fig. 2: The tables showing the results from the MM2 energy minimisation. 1 is on the left and 2 is on the right. current
• 21:5621:56, 3 March 2011 diff hist −28 Mod.timarbab →The Hydrogenation of Cyclopentadiene
• 21:5621:56, 3 March 2011 diff hist +38 N File:Picture 1timarbab.jpg Fig. 1: The mechanism and two products current
• 21:3721:37, 3 March 2011 diff hist +604 Mod.timarbab No edit summary
• 21:3321:33, 3 March 2011 diff hist 0 N File:Timmyboy2.mol No edit summary current
• 21:3221:32, 3 March 2011 diff hist +2 Mod.timarbab No edit summary
• 21:3221:32, 3 March 2011 diff hist −1 Mod.timarbab →The Hydrogenation of Cyclopentadiene
• 21:3221:32, 3 March 2011 diff hist +38 Mod.timarbab No edit summary
• 21:2921:29, 3 March 2011 diff hist 0 N File:Picture1timmyboy.png No edit summary current

28 February 2011

• 17:1417:14, 28 February 2011 diff hist +323 Mod.timarbab No edit summary
• 16:2616:26, 28 February 2011 diff hist +2 Mod.timarbab No edit summary
• 16:2616:26, 28 February 2011 diff hist +742 N Mod.timarbab New page: === Level 3 ==='''The Hydrogenation of Cyclopentadiene''' Cyclopentadiene can dimerise, in a cycloaddition reaction, to form two different stereoisomers. These are the endo and exo forms...