User contributions for Tna08

4 March 2011

• 19:0419:04, 4 March 2011 diff hist +14 Mod.timarbab →Regioselective Addition of Dichlorocarbene
• 19:0419:04, 4 March 2011 diff hist +28 Mod.timarbab →Stereochemistry and Reactivity of an Intermediate in the Synthesis of Taxol
• 19:0219:02, 4 March 2011 diff hist −21 Mod.timarbab →Nucleophilic addition of NHPhenyl group to a pyridinium ring
• 18:5918:59, 4 March 2011 diff hist +10 Mod.timarbab →Nucleophilic addition of NHPhenyl group to a pyridinium ring
• 18:5618:56, 4 March 2011 diff hist +16 Mod.timarbab →Nucleophilic addition of NHPhenyl group to a pyridinium ring
• 18:5318:53, 4 March 2011 diff hist +485 Mod.timarbab →Regioselective Addition of Dichlorocarbene
• 16:5916:59, 4 March 2011 diff hist +154 Mod.timarbab →Regioselective Addition of Dichlorocarbene
• 16:4916:49, 4 March 2011 diff hist +524 Mod.timarbab →Regioselective Addition of Dichlorocarbene
• 16:4316:43, 4 March 2011 diff hist +116 Mod.timarbab →Regioselective Addition of Dichlorocarbene
• 16:3916:39, 4 March 2011 diff hist +84 Mod.timarbab →Modelling Using Semi-Emperical Molecular Orbital Theory
• 16:3916:39, 4 March 2011 diff hist +179 N File:Picture 15 MOs of 12 from PM6.jpg Fig. 15: The molecular orbitals obtained using PM6. The top row is, from left to right, HOMO-2, HOMO-1 and HOMO. The bottom row is, from left to right, LUMO, LUMO+1 and LUMO+2. current
• 16:3816:38, 4 March 2011 diff hist +94 N File:Picture 14 reaction of 12 and CCl2.jpg Fig. 14: The reaction of molecule 12 and dichlorocarbene to form either the di or mono adduct. current
• 16:3716:37, 4 March 2011 diff hist +359 Mod.timarbab →Modelling Using Semi-Emperical Molecular Orbital Theory
• 16:3616:36, 4 March 2011 diff hist +31 N File:12 mol.mol Fig. 13: A Jmol of molecule 12. current
• 16:3016:30, 4 March 2011 diff hist +912 Mod.timarbab →Modelling Using Semi-Emperical Molecular Orbital Theory
• 15:0015:00, 4 March 2011 diff hist +141 Mod.timarbab →Stereochemistry and Reactivity of an Intermediate in the Synthesis of Taxol
• 14:5814:58, 4 March 2011 diff hist +429 Mod.timarbab →Stereochemistry and Reactivity of an Intermediate in the Synthesis of Taxol
• 14:5614:56, 4 March 2011 diff hist +43 N File:10 alkane mol.mol Fig. 12: The alkane related to molecule 10. current
• 14:5314:53, 4 March 2011 diff hist +696 Mod.timarbab →Stereochemistry and Reactivity of an Intermediate in the Synthesis of Taxol
• 14:3314:33, 4 March 2011 diff hist +5 Mod.timarbab →Stereochemistry and Reactivity of an Intermediate in the Synthesis of Taxol
• 14:3214:32, 4 March 2011 diff hist +109 N File:Picture 10 9 and 10 energy table final.jpg Fig. 10: The Total Energy achieved for the two atropisomers, 9 and 10, when using two different force fields. current
• 14:2914:29, 4 March 2011 diff hist +3 Mod.timarbab →Stereochemistry and Reactivity of an Intermediate in the Synthesis of Taxol
• 14:2614:26, 4 March 2011 diff hist +322 Mod.timarbab →Stereochemistry and Reactivity of an Intermediate in the Synthesis of Taxol
• 14:1614:16, 4 March 2011 diff hist +19 Mod.timarbab →Stereochemistry and Reactivity of an Intermediate in the Synthesis of Taxol
• 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