The following pages link to Chem. Rev.
External toolsShowing 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Wohl–Ziegler bromination (links | edit)
- Barton–McCombie deoxygenation (links | edit)
- Hyperconjugation (links | edit)
- Nitrosonium (links | edit)
- Rev (links | edit)
- Atom transfer radical polymerization (links | edit)
- Arndt–Eistert reaction (links | edit)
- Triazole (links | edit)
- Wagner–Meerwein rearrangement (links | edit)
- Polyhedral skeletal electron pair theory (links | edit)
- Betti reaction (links | edit)
- Bredt's rule (links | edit)
- Friedländer synthesis (links | edit)
- Niementowski quinoline synthesis (links | edit)
- Stollé synthesis (links | edit)
- Danishefsky Taxol total synthesis (links | edit)
- Persistent carbene (links | edit)
- Petasis reaction (links | edit)
- Paul-Antoine Giguère (links | edit)
- Horner–Wadsworth–Emmons reaction (links | edit)
- Blaise ketone synthesis (links | edit)
- Hunsdiecker reaction (links | edit)
- Lossen rearrangement (links | edit)
- Bergman cyclization (links | edit)
- Doebner–Miller reaction (links | edit)
- Aromatic ring current (links | edit)
- Finkelstein reaction (links | edit)
- Antimony pentachloride (links | edit)
- Polythiazyl (links | edit)
- Galantamine total synthesis (links | edit)
- Hammett equation (links | edit)
- Bond valence method (links | edit)
- Hapticity (links | edit)
- Heat of formation group additivity (links | edit)
- Trioxidane (links | edit)
- Chiral derivatizing agent (links | edit)
- Iodine compounds (links | edit)
- Conrad–Limpach synthesis (links | edit)
- Grimm's hydride displacement law (links | edit)
- Oppenauer oxidation (links | edit)
- Elbs persulfate oxidation (links | edit)
- Fenestrane (links | edit)
- Franz Hein (links | edit)
- Combes quinoline synthesis (links | edit)
- Urech hydantoin synthesis (links | edit)
- Tropone (links | edit)
- Tropolone (links | edit)
- Meyer–Schuster rearrangement (links | edit)
- Allylic strain (links | edit)
- Ligand cone angle (links | edit)