Gareth Rowlands

chemistry organic organicchemistry organic synthesis asymmetric synthesis organic chemistry retrosynthesis total synthesis education synthesis disconnections chirality substrate control enantioselective catalysis alkenes totalsynthesis enantioselectivity shape chiral organocatalysis asymmetric catalysis chemistryoflivingsystems enantiomers stereochemistry chiral reagents chiral auxiliaries epothilone functionalgroupinterconversions aldol carbonyl reduction oxidation spectroscopy bonding orbitals radical chemistry radical educacion catalysis higher education pharmaceutical sweeteners drugs natural products dienes alkynes hydrogenbonding intermolecularforces resonancehybrids resonancestructures chairconformation boatconformation chemistrylivingofsystems nuclearmagneticspectroscopy infraredspectroscopy massspectrometry carboxylicacids protectinggroups carboxylicacidderivatives hydridereducingreagents c-cbondformation functionalgroupinterconversion conjugateadditions michaeladditions fattyacids callipeltosidec triglycerides enolates 14-additions wittig enolate mechanisms organic_chemistry functional_groups susbtitution alcohols baeyer-villiger fats oils ir diastereoiosmers nmr cyclohexane strain conformations reagents reactions dipoles solubility polarity resonance length strength bond names functional groups fg introduction electrons handedness molecules shapes science