chempirical
Reaction database

Reactions

3,374 reactions: 10 worked examples with a reagent table you can scale, 503 named reactions and 2,861 checked procedures from Organic Syntheses.

1,153–1,176 of 3,374

  1. Conversion of nitriles into tertiary amines: N,N-dimethylhomoveratrylamine Org. Synth. Vol. 76, p. 133 · Rousselet et al.
  2. Conversion of nitro to carbonyl by ozonolysis of nitronates: 2,5-heptanedioneOxidation Org. Synth. Coll. Vol. 6, p. 648; Vol. 56, p. 36 · McMurry and Melton
  3. Conversion of primary alcohols to urethanes via the inner salt of methyl (carboxysulfamoyl)triethylammonium hydroxide: methyl n-hexylcarbamate Org. Synth. Coll. Vol. 6, p. 788; Vol. 56, p. 40 · Burgess et al.
  4. Copper catalyzed arylation of β-dicarbonyl compounds: 2-(1-acetyl-2-oxopropyl)benzoic acid Org. Synth. Coll. Vol. 6, p. 36; Vol. 58, p. 52 · Bruggink et al.
  5. Copper chromite catalyst Org. Synth. Coll. Vol. 2, p. 142; Vol. 19, p. 31 · Lazier and Arnold
  6. Copper-catalyzed conjugate addition of a zinc homoenolate: ethyl 3-[3-(trimethylsilyloxy)cyclohex-2-enyl]propionateAddition Org. Synth. Coll. Vol. 8, p. 277; Vol. 66, p. 43 · Nakamura and Kuwajima
  7. Copper-catalyzed conjugate addition of functionalized organozinc reagents to α,β-unsaturated ketones: ethyl 5-(3-oxocyclohexyl)pentanoateAddition Org. Synth. Vol. 76, p. 252 · Lipshutz et al.
  8. Copper-catalyzed electrophilic amination of diorganozinc reagents: 4-phenylmorpholine Org. Synth. Vol. 83, p. 31 · Berman and Johnson
  9. Copper-catalyzed three-component reaction of 1-alkynes, sulfonyl azides, and water: N-(4-acetamidophenylsulfonyl)-2-phenylacetamide Org. Synth. Vol. 85, p. 131 · Cho et al.
  10. Copper(I) iodide dimethyl sulfide catalyzed addition of a vinylzirconium reagent (preparation of 4-phenyl-5(E)-decen-2-one)Addition Org. Synth. Vol. 84, p. 192 · El-Batta and Bergdahl
  11. Copper(I)-catalyzed photocycloaddition: 3,3-dimethyl-cis-bicyclo[3.2.0]heptan-2-oneCycloaddition Org. Synth. Coll. Vol. 7, p. 177; Vol. 62, p. 125 · Salomon and Ghosh
  12. Copper(I)-catalyzed preparation of (E)-3-iodoprop-2-enoic acid Org. Synth. Vol. 80, p. 129 · Dixon et al.
  13. Coumalic acid Org. Synth. Coll. Vol. 4, p. 201; Vol. 31, p. 23 · Wiley and Smith
  14. Coumarilic acid Org. Synth. Coll. Vol. 3, p. 209; Vol. 24, p. 33 · Fuson et al.
  15. Coumarone Org. Synth. Coll. Vol. 5, p. 251; Vol. 46, p. 28 · Burgstahler and Worden
  16. Coupling of o-tolidine and chicago acidCross-coupling Org. Synth. Coll. Vol. 2, p. 145; Vol. 16, p. 12 · Hartwell and Fieser
  17. Creatinine Org. Synth. Coll. Vol. 1, p. 172; Vol. 4, p. 15 · Edgar and Hinegardner
  18. Creosol Org. Synth. Coll. Vol. 4, p. 203; Vol. 33, p. 17 · Schwarz and Hering
  19. p-Cresol Org. Synth. Coll. Vol. 1, p. 175; Vol. 3, p. 37 · Hartman
  20. Cross-Coupling of Alkenyl/Aryl Carboxylates with Grignard Reagents via Fe-Catalyzed C-O Bond ActivationOrganometallic addition Org. Synth. Vol. 91, p. 83 · Li et al.
  21. γ-Crotonolactone Org. Synth. Coll. Vol. 5, p. 255; Vol. 45, p. 22 · Price and Judge
  22. Crotyl diazoacetate Org. Synth. Coll. Vol. 5, p. 258; Vol. 49, p. 22 · Blankley et al.
  23. 18-Crown-6 Org. Synth. Coll. Vol. 6, p. 301; Vol. 57, p. 30 · Gokel et al.
  24. Cu-catalyzed azide-alkyne cycloaddition: preparation of tris((1-benzyl-1H-1,2,3-triazolyl)methyl)amineCycloaddition Org. Synth. Vol. 88, p. 238 · Hein et al.