The following pages link to J. Org. Chem.
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Alkyne (links | edit)
- Chromatography (links | edit)
- Ferrocene (links | edit)
- Cyclopentadiene (links | edit)
- Acetoacetic acid (links | edit)
- Ethylene glycol (links | edit)
- Swern oxidation (links | edit)
- Sharpless asymmetric dihydroxylation (links | edit)
- Pyrrole (links | edit)
- Porphyrin (links | edit)
- Isomerization (links | edit)
- Maillard reaction (links | edit)
- Precipitation (chemistry) (links | edit)
- Oxime (links | edit)
- Chromic acid (links | edit)
- Epoxide (links | edit)
- Thiophene (links | edit)
- Ylide (links | edit)
- Diol (links | edit)
- Organolithium reagent (links | edit)
- Protecting group (links | edit)
- Nitration (links | edit)
- Hexanitrobenzene (links | edit)
- Sodium azide (links | edit)
- Heck reaction (links | edit)
- Suzuki reaction (links | edit)
- Electrocyclic reaction (links | edit)
- Sonogashira coupling (links | edit)
- Formamide (links | edit)
- Dendrimer (links | edit)
- Enantioselective synthesis (links | edit)
- Carbo-mer (links | edit)
- Cyclohexane conformation (links | edit)
- Nitrene (links | edit)
- Thiazole (links | edit)
- Dodecahedrane (links | edit)
- Simmons–Smith reaction (links | edit)
- Raney nickel (links | edit)
- Gabriel synthesis (links | edit)
- 1,2-rearrangement (links | edit)
- Organopalladium chemistry (links | edit)
- Sandmeyer reaction (links | edit)
- Enantiomeric excess (links | edit)
- AD-mix (links | edit)
- N-Bromosuccinimide (links | edit)
- Dess–Martin periodinane (links | edit)
- Trimethylsilyl group (links | edit)
- Bernthsen acridine synthesis (links | edit)
- Camps quinoline synthesis (links | edit)
- Pictet–Spengler reaction (links | edit)