The following pages link to The Journal of Organic Chemistry
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- American Chemical Society (links | edit)
- Friedel–Crafts reaction (links | edit)
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- Azulene (links | edit)
- List of organic reactions (links | edit)
- Journal of the American Chemical Society (links | edit)
- Fischer oxazole synthesis (links | edit)
- Azide-alkyne Huisgen cycloaddition (links | edit)
- Hiyama coupling (links | edit)
- Corey–Itsuno reduction (links | edit)
- Knorr pyrrole synthesis (links | edit)
- Reformatsky reaction (links | edit)
- J. Org. Chem. (redirect page) (links | edit)
- 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)
- Organoboron chemistry (links | edit)
- 9-Borabicyclo(3.3.1)nonane (links | edit)
- Claisen rearrangement (links | edit)
- Pentane interference (links | edit)
- Gold(III) chloride (links | edit)
- Bouveault aldehyde synthesis (links | edit)
- Bodroux–Chichibabin aldehyde synthesis (links | edit)
- Blaise reaction (links | edit)
- Fritsch–Buttenberg–Wiechell rearrangement (links | edit)
- Carbodiimide (links | edit)
- Cheletropic reaction (links | edit)
- Phosphoric acids and phosphates (links | edit)
- Japp–Klingemann reaction (links | edit)
- Tetrazole (links | edit)
- Leimgruber–Batcho indole synthesis (links | edit)
- Bouveault–Blanc reduction (links | edit)
- Carbon tetrafluoride (links | edit)
- Cyanuric chloride (links | edit)
- Menshutkin reaction (links | edit)
- Meldrum's acid (links | edit)
- CBS catalyst (links | edit)
- (E)-Stilbene (links | edit)
- Overman rearrangement (links | edit)
- Ruthenium(III) chloride (links | edit)
- Biginelli reaction (links | edit)
- Chiral auxiliary (links | edit)
- Trans-2-Phenyl-1-cyclohexanol (links | edit)
- Bingel reaction (links | edit)
- Arndt–Eistert reaction (links | edit)
- Triazole (links | edit)
- 1,2,3-Triazole (links | edit)
- Betti reaction (links | edit)
- Silver(II) fluoride (links | edit)
- Bredt's rule (links | edit)
- Longifolene (links | edit)
- Jacobsen epoxidation (links | edit)
- Dowd–Beckwith ring-expansion reaction (links | edit)
- Favorskii rearrangement (links | edit)
- Camphorsulfonic acid (links | edit)
- Peterson olefination (links | edit)
- Discodermolide (links | edit)
- Grieco elimination (links | edit)
- Pyramidal alkene (links | edit)
- Di-tert-butyl dicarbonate (links | edit)
- Seyferth–Gilbert homologation (links | edit)
- Wharton reaction (links | edit)
- Acyloin (links | edit)
- Horner–Wadsworth–Emmons reaction (links | edit)
- 2-Pyridone (links | edit)
- Phosphite ester (links | edit)
- Paclitaxel total synthesis (links | edit)
- List of Georgia Institute of Technology faculty (links | edit)
- Bartoli indole synthesis (links | edit)
- Pentamethylcyclopentadiene (links | edit)
- Tebbe's reagent (links | edit)
- Benzilic acid rearrangement (links | edit)
- Baldwin's rules (links | edit)
- Reactivity–selectivity principle (links | edit)
- Palladium dicyanide (links | edit)
- 1,2-Bis(diphenylphosphino)ethane (links | edit)
- Allan–Robinson reaction (links | edit)
- Ivanov reaction (links | edit)
- Directed ortho metalation (links | edit)
- Xenon difluoride (links | edit)
- Norrish reaction (links | edit)
- Tert-Butyloxycarbonyl protecting group (links | edit)
- Galantamine total synthesis (links | edit)
- Julia olefination (links | edit)
- Hammett equation (links | edit)
- Copper(II) bromide (links | edit)
- Heat of formation group additivity (links | edit)
- Schwartz's reagent (links | edit)
- Scholl reaction (links | edit)
- Corey–Winter olefin synthesis (links | edit)
- Aziridines (links | edit)
- Chiral derivatizing agent (links | edit)
- Propellane (links | edit)
- Oppenauer oxidation (links | edit)
- Boyland–Sims oxidation (links | edit)
- Thorpe–Ingold effect (links | edit)
- Sharpless oxyamination (links | edit)
- Radialene (links | edit)
- Buchwald–Hartwig amination (links | edit)
- Fluxional molecule (links | edit)
- Hammick reaction (links | edit)
- Angeli–Rimini reaction (links | edit)
- Gomberg–Bachmann reaction (links | edit)
- Dimethyl carbonate (links | edit)
- Eschenmoser fragmentation (links | edit)
- Isotoluene (links | edit)
- Lanthanide trifluoromethanesulfonates (links | edit)
- Tropone (links | edit)
- Diphenylketene (links | edit)
- Annulation (links | edit)
- Meyer–Schuster rearrangement (links | edit)
- Allylic strain (links | edit)
- Reduction of nitro compounds (links | edit)
- Zincke aldehyde (links | edit)
- Non-mevalonate pathway (links | edit)
- Nickel oxide hydroxide (links | edit)
- Carbometalation (links | edit)
- Westphalen–Lettré rearrangement (links | edit)
- Oseltamivir total synthesis (links | edit)
- Skattebøl rearrangement (links | edit)
- Foiled carbene (links | edit)
- 2-Methyl-2-nitrosopropane (links | edit)
- Hydrosilanes (links | edit)
- Meerwein arylation (links | edit)
- Castro–Stephens coupling (links | edit)
- Collins reagent (links | edit)
- Baudisch reaction (links | edit)
- 2-Aminothiazole (links | edit)
- Cylindrospermopsin (links | edit)
- L-selectride (links | edit)
- Homologation reaction (links | edit)
- Bite angle (links | edit)
- Lemieux–Johnson oxidation (links | edit)
- Sodium methylsulfinylmethylide (links | edit)
- Woodward's rules (links | edit)
- Methanesulfonyl chloride (links | edit)
- Koch reaction (links | edit)
- Baker–Nathan effect (links | edit)
- Biphenylene (links | edit)
- Knorr quinoline synthesis (links | edit)
- Diketene (links | edit)
- 2-Acetyl-1-pyrroline (links | edit)
- 6-Acetyl-2,3,4,5-tetrahydropyridine (links | edit)
- Cis-Cyclooctene (links | edit)
- Hofmann–Löffler reaction (links | edit)
- Pirkle's alcohol (links | edit)
- Tetraphenylcyclopentadienone (links | edit)
- Fleming–Tamao oxidation (links | edit)
- Valence isomer (links | edit)
- Zinc–copper couple (links | edit)
- Sodium tetraphenylborate (links | edit)
- Silver trifluoromethanesulfonate (links | edit)
- Trifluoroacetic anhydride (links | edit)
- N-Chlorosuccinimide (links | edit)
- Diisopinocampheylborane (links | edit)
- Alpine borane (links | edit)
- Kelliphite (links | edit)
- Hyponitrite (links | edit)
- Hypervalent organoiodine compounds (links | edit)
- Liebeskind–Srogl coupling (links | edit)
- Ferrier carbocyclization (links | edit)
- 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide (links | edit)
- Zinc triflate (links | edit)
- Dess–Martin oxidation (links | edit)
- Tetraphenylporphyrin (links | edit)
- Triisopropylamine (links | edit)
- Indole (links | edit)
- Strychnine total synthesis (links | edit)
- Eaton's reagent (links | edit)
- Carbene C−H insertion (links | edit)
- Borane dimethylsulfide (links | edit)
- Swain–Lupton equation (links | edit)
- Markó–Lam deoxygenation (links | edit)
- Vinod K. Singh (links | edit)
- Alcohol oxidation (links | edit)
- Α-Ketol rearrangement (links | edit)
- Enone–alkene cycloadditions (links | edit)
- Dimethylmagnesium (links | edit)
- Oxidation with chromium(VI) complexes (links | edit)
- Synthesis of nucleosides (links | edit)
- Taxodone (links | edit)
- Diphenylzinc (links | edit)
- (1,1'-Bis(diphenylphosphino)ferrocene)palladium(II) dichloride (links | edit)
- Pinnick oxidation (links | edit)
- Insertion reaction (links | edit)
- Saegusa–Ito oxidation (links | edit)
- Edward M. Burgess (links | edit)
- PEPPSI (links | edit)
- Cholesterol total synthesis (links | edit)
- Hexamethylbenzene (links | edit)
- Radical disproportionation (links | edit)
- Electrophilic aromatic substitution (links | edit)
- Buchner ring expansion (links | edit)
- Acyl azide (links | edit)
- Van Leusen reaction (links | edit)
- 1-Tetralone (links | edit)
- 2-Methyl-6-nitrobenzoic anhydride (links | edit)
- Asymmetric addition of alkynylzinc compounds to aldehydes (links | edit)
- Shiina macrolactonization (links | edit)
- Oxy-Cope rearrangement (links | edit)
- Shiina esterification (links | edit)
- Tetramethylurea (links | edit)
- N-Hydroxyphthalimide (links | edit)
- 4-Formylphenylboronic acid (links | edit)
- P4-t-Bu (links | edit)
- Trifluoroperacetic acid (links | edit)
- Tamejiro Hiyama (links | edit)
- Propynyllithium (links | edit)
- Ynone (links | edit)
- Fluoroacetone (links | edit)
- Trifluoroacetone (links | edit)
- Pentachlorobenzenethiol (links | edit)
- (Diacetoxyiodo)benzene (links | edit)
- Diethylphosphite (links | edit)
- 1,2,4,5-Tetrabromobenzene (links | edit)
- 2-Carboxybenzaldehyde (links | edit)
- Cyclooctene (links | edit)
- 3-Dimethylaminoacrolein (links | edit)
- 2-Methyleneglutaronitrile (links | edit)
- Itaconic anhydride (links | edit)
- Tetrakis(dimethylamino)ethylene (links | edit)
- Bobbitt reaction (links | edit)
- Peroxymonophosphoric acid (links | edit)
- Organic azide (links | edit)
- 1,4-Pentadiyne (links | edit)
- Glycerol-1,2-carbonate (links | edit)
- 2-Cumaranone (links | edit)
- Talk:J. Org. Chem. (links | edit)
- Talk:Yohimbine/Archive 1 (links | edit)
- User:Rifleman 82/Heck reaction (links | edit)
- User:Beetstra/ReactionBox (links | edit)
- User:Chem540f09grp10/Sandbox (links | edit)
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- User:Bernanke's Crossbow/Schutzgruppe (links | edit)
- Misplaced Pages:Version 1.0 Editorial Team/Chemistry articles by quality log (links | edit)
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- Reissert reaction (links | edit)
- The Journal of Physical Chemistry A (links | edit)
- The Journal of Physical Chemistry B (links | edit)
- Chemical Reviews (links | edit)
- Journal of Medicinal Chemistry (links | edit)
- ACS Combinatorial Science (links | edit)
- Organic Letters (links | edit)
- Accounts of Chemical Research (links | edit)
- Johnson–Corey–Chaykovsky reaction (links | edit)
- Weinreb ketone synthesis (links | edit)
- Umpolung (links | edit)
- Analytical Chemistry (journal) (links | edit)
- Transfer hydrogenation (links | edit)
- Langmuir (journal) (links | edit)
- Inorganic Chemistry (journal) (links | edit)
- Nazarov cyclization reaction (links | edit)
- Journal of Chemical Information and Modeling (links | edit)
- Paal–Knorr synthesis (links | edit)
- Ammonium tetrathiomolybdate (links | edit)
- Balz–Schiemann reaction (links | edit)
- Wurtz–Fittig reaction (links | edit)
- JOC (links | edit)
- Journal of Chemical Education (links | edit)
- Industrial & Engineering Chemistry Research (links | edit)
- Organometallics (links | edit)
- Deuterated DMSO (links | edit)
- Sulfolene (links | edit)
- Environmental Science & Technology (links | edit)
- ACS Chemical Biology (links | edit)
- The Journal of Physical Chemistry C (links | edit)
- Asymmetric hydrogenation (links | edit)
- Horsfiline (links | edit)
- Biochemistry (journal) (links | edit)
- ACS Applied Materials & Interfaces (links | edit)
- Chemistry of Materials (links | edit)
- ACS Nano (links | edit)