chempirical
Reaction database

Organic Syntheses procedures

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

1,441–1,464 of 2,861

  1. 2,3,4,5,6,6-Hexamethyl-2,4-cyclohexadien-1-one Org. Synth. Coll. Vol. 5, p. 598; Vol. 48, p. 87 · Hart et al.
  2. Hexamethylbenzene Org. Synth. Coll. Vol. 4, p. 520; Vol. 35, p. 73 · Cullinane et al.
  3. Hexamethylene chlorohydrin Org. Synth. Coll. Vol. 3, p. 446; Vol. 28, p. 65 · Campbell and Sommers
  4. Hexamethylene diisocyanate Org. Synth. Coll. Vol. 4, p. 521; Vol. 31, p. 62 · Farlow
  5. Hexamethylene glycol Org. Synth. Coll. Vol. 2, p. 325; Vol. 19, p. 48 · Lazier et al.
  6. Hexamethylphosphorous triamide Org. Synth. Coll. Vol. 5, p. 602; Vol. 46, p. 42 · Mark
  7. Hexaphenylbenzene Org. Synth. Coll. Vol. 5, p. 604; Vol. 46, p. 44 · Fieser
  8. 1,3,5-Hexatriene Org. Synth. Coll. Vol. 5, p. 608; Vol. 41, p. 49 · Hwa and Sims
  9. (E)-4-Hexen-1-ol Org. Synth. Coll. Vol. 6, p. 675; Vol. 55, p. 62 · Paul et al.
  10. n-Hexyl alcohol Org. Synth. Coll. Vol. 1, p. 306; Vol. 6, p. 54 · Dreger
  11. n-Hexyl fluoride Org. Synth. Coll. Vol. 4, p. 525; Vol. 36, p. 40 · Vogel et al.
  12. High-yielding, large-scale synthesis of N-protected-β-aminonitriles: tert-butyl (1R)-2-cyano-1-phenylethylcarbamate Org. Synth. Vol. 85, p. 219 · Mosa et al.
  13. Highly efficient addition of activated methylene compounds to alkenes catalyzed by gold and silverAddition Org. Synth. Vol. 84, p. 222 · Li and Yao
  14. Highly reactive calcium for the preparation of organocalcium reagents: 1-adamantyl calcium halides and their addition to ketones: 1-(1-adamantyl)cyclohexanolAddition Org. Synth. Coll. Vol. 9, p. 9; Vol. 72, p. 147 · Rieke et al.
  15. Highly reactive magnesium for the preparation of Grignard reagents: 1-norbornanecarboxylic acidOrganometallic addition Org. Synth. Coll. Vol. 6, p. 845; Vol. 59, p. 85 · Rieke et al.
  16. Hippuric acid Org. Synth. Coll. Vol. 2, p. 328; Vol. 12, p. 40 · Ingersoll and Babcock
  17. l-Histidine monohydrochloride Org. Synth. Coll. Vol. 2, p. 330; Vol. 18, p. 43 · Foster and Shemin
  18. 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.
  19. 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
  20. Homogeneous catalytic hydrogenation: dihydrocarvoneReduction Org. Synth. Coll. Vol. 6, p. 459; Vol. 53, p. 63 · Ireland and Bey
  21. Homophthalic acid Org. Synth. Coll. Vol. 5, p. 612; Vol. 44, p. 62 · Smith and Kan
  22. Homophthalic acid and anhydride Org. Synth. Coll. Vol. 3, p. 449; Vol. 29, p. 49 · Grummitt et al.
  23. Homoveratric acid Org. Synth. Coll. Vol. 2, p. 333; Vol. 15, p. 31 · Snyder et al.
  24. Hydrazine sulfate Org. Synth. Coll. Vol. 1, p. 309; Vol. 2, p. 37 · Adams and Brown