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.

1,969–1,992 of 3,374

  1. Hippuric acid Org. Synth. Coll. Vol. 2, p. 328; Vol. 12, p. 40 · Ingersoll and Babcock
  2. l-Histidine monohydrochloride Org. Synth. Coll. Vol. 2, p. 330; Vol. 18, p. 43 · Foster and Shemin
  3. Hofmann rearrangement under mildly acidic conditions using [I,I-bis(trifluoroacetoxy)]iodobenzene: cyclobutylamine hydrochloride from cyclobutanecarboxamideRearrangement Org. Synth. Coll. Vol. 8, p. 132; Vol. 66, p. 132 · Almond et al.
  4. Homoconjugate addition of nucleophiles to cyclopropane-1,1-dicarboxylate derivatives: 2-oxo-1-phenyl-3-pyrrolidinecarboxylic acidAddition Org. Synth. Coll. Vol. 7, p. 411; Vol. 60, p. 66 · Singh and Danishefsky
  5. Homogeneous catalytic hydrogenation: dihydrocarvoneReduction Org. Synth. Coll. Vol. 6, p. 459; Vol. 53, p. 63 · Ireland and Bey
  6. Homophthalic acid Org. Synth. Coll. Vol. 5, p. 612; Vol. 44, p. 62 · Smith and Kan
  7. Homophthalic acid and anhydride Org. Synth. Coll. Vol. 3, p. 449; Vol. 29, p. 49 · Grummitt et al.
  8. Homoveratric acid Org. Synth. Coll. Vol. 2, p. 333; Vol. 15, p. 31 · Snyder et al.
  9. Hydrazine sulfate Org. Synth. Coll. Vol. 1, p. 309; Vol. 2, p. 37 · Adams and Brown
  10. α-Hydrindone Org. Synth. Coll. Vol. 2, p. 336; Vol. 18, p. 47 · Pacaud and Allen
  11. Hydrocinnamic acid Org. Synth. Coll. Vol. 1, p. 311; Vol. 9, p. 42 · Ingersoll
  12. Hydrogen bromide (anhydrous) Org. Synth. Coll. Vol. 2, p. 338; Vol. 15, p. 35 · Ruhoff et al.
  13. Hydrogen cyanide (anhydrous) Org. Synth. Coll. Vol. 1, p. 314; Vol. 7, p. 50 · Ziegler
  14. Hydrogenation of aromatic nuclei: 1-decalolReduction Org. Synth. Coll. Vol. 6, p. 371; Vol. 51, p. 103 · Meyers et al.
  15. Hydrogenolysis of carbon-halogen bonds with chromium(II)-en perchlorate: naphthalene from 1-bromonaphthalene Org. Synth. Coll. Vol. 6, p. 821; Vol. 52, p. 62 · Wade and Castro
  16. Hydromagnesiation reaction of propargylic alcohols: (E)-3-pentyl-2-nonene-1,4-diol from 2-octyn-1-ol Org. Synth. Coll. Vol. 8, p. 507; Vol. 69, p. 106 · Sato and Kobayashi
  17. Hydroquinone diacetate Org. Synth. Coll. Vol. 3, p. 452; Vol. 28, p. 68 · Prichard
  18. β-Hydroxy esters from ethyl acetate and aldehydes or ketones: ethyl 1-hydroxycyclohexylacetate Org. Synth. Coll. Vol. 6, p. 598; Vol. 53, p. 66 · Rathke
  19. α-Hydroxy ketones from the oxidation of enol silyl ethers with m-chloroperbenzoic acid: 6-hydroxy- 3,5,5-trimethyl-2-cyclohexen-1-oneOxidation Org. Synth. Coll. Vol. 7, p. 282; Vol. 64, p. 118 · Rubottom et al.
  20. 4-Hydroxy-1-butanesulfonic acid sultone Org. Synth. Coll. Vol. 4, p. 529; Vol. 37, p. 55 · Snoddy
  21. 3-Hydroxy-1-cyclohexene-1-carboxaldehyde Org. Synth. Coll. Vol. 8, p. 309; Vol. 67, p. 205 · Rigby et al.
  22. 2-Hydroxy-1-naphthaldehyde Org. Synth. Coll. Vol. 3, p. 463; Vol. 22, p. 63 · Russell and Lockhart
  23. (R)-(+)-2-Hydroxy-1,2,2-triphenylethyl acetate Org. Synth. Coll. Vol. 9, p. 507; Vol. 72, p. 32 · Braun et al.
  24. (R)-(+)-2-Hydroxy-1,2,2-triphenylethyl acetate Org. Synth. Vol. 77, p. 45 · Macor et al.