Talk:Mod:LIUXYLANA1

Cpd dimers: Excellent.

Taxol: It is not good enough to simply state that the alkene is hyperstable, where is your evidence? Good to see you investigating different conformations of the six membered ring, however.

Carbene: You’ve done the calculations, but where is the analysis? Okay, you’ve identified which of the two alkenes are more electron rich, but why has this happened?

Glycosidation: Good energies, but where is the analysis? Your jmol links are broken.

Taxol NMR: Where is the comparison to the literature values?

Mini-project: Some jmols of your structures would have been nice. What ring current? There is no aromatic ring. A better comparison here is needed between your results and the literature. Comparing your results in a table, or better yet a bar chart, would have been good. What’s the conclusion? Was modelling the NMR data useful? Could we use it to tell the isomers apart?

Overall: Your report started off so well, what happened?