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.

1,273–1,296 of 3,374

  1. Desyl chloride Org. Synth. Coll. Vol. 2, p. 159; Vol. 12, p. 20 · Ward
  2. Detrifluoroacetylative diazo group transfer: (E)-1-diazo-4-phenyl-3-buten-2-one Org. Synth. Coll. Vol. 9, p. 197; Vol. 73, p. 134 · Danheiser et al.
  3. Di-(p-chlorophenyl)acetic acid Org. Synth. Coll. Vol. 3, p. 270; Vol. 26, p. 21 · Grummitt et al.
  4. 1,2-Di-1-(1-cyano)cyclohexylhydrazine Org. Synth. Coll. Vol. 4, p. 274; Vol. 32, p. 50 · Overberger et al.
  5. β-Di-n-butylaminoethylamine Org. Synth. Coll. Vol. 3, p. 254; Vol. 23, p. 23 · Amundsen et al.
  6. γ-Di-n-butylaminopropylamine Org. Synth. Coll. Vol. 3, p. 256; Vol. 24, p. 44 · Amundsen and Sanderson
  7. Di-n-butylcarbinol Org. Synth. Coll. Vol. 2, p. 179; Vol. 15, p. 11 · Coleman and Craig
  8. Di-n-butyldivinyltin Org. Synth. Coll. Vol. 4, p. 258; Vol. 39, p. 10 · Seyferth
  9. 1,4-Di-O-alkyl threitols from tartaric acid: 1,4-di-O-benzyl-L-threitol Org. Synth. Coll. Vol. 8, p. 155; Vol. 68, p. 92 · Mash et al.
  10. Di-o-nitrophenyl disulfide Org. Synth. Coll. Vol. 1, p. 220; Vol. 8, p. 64 · Bogert and Stull
  11. 1,1-Di-p-tolylethane Org. Synth. Coll. Vol. 1, p. 229; Vol. 4, p. 23 · Reichert and Nieuwland
  12. Di-p-tolylmercury Org. Synth. Coll. Vol. 1, p. 231; Vol. 3, p. 65 · Whitmore et al.
  13. Di-t-butyl nitroxide Org. Synth. Coll. Vol. 5, p. 355; Vol. 48, p. 62 · Hoffmann et al.
  14. Di-tert-butyl dicarbonate Org. Synth. Coll. Vol. 6, p. 418; Vol. 57, p. 45 · Pope et al.
  15. Di-tert-butyl malonate Org. Synth. Coll. Vol. 4, p. 261; Vol. 34, p. 26 · McCloskey et al.
  16. Di-tert-butyl methylenemalonate Org. Synth. Coll. Vol. 7, p. 142; Vol. 64, p. 63 · Ballesteros and Roberts
  17. 2,6-Di-tert-butyl-4-methylpyridine Org. Synth. Coll. Vol. 7, p. 144; Vol. 60, p. 34 · Anderson and Stang
  18. Di-β-carbethoxyethylmethylamine Org. Synth. Coll. Vol. 3, p. 258; Vol. 20, p. 35 · Mozingo and McCracken
  19. Diacetonamine hydrogen oxalate Org. Synth. Coll. Vol. 1, p. 196; Vol. 6, p. 28 · Haeseler
  20. Diacetone alcohol Org. Synth. Coll. Vol. 1, p. 199; Vol. 1, p. 45 · Conant and Tuttle
  21. 3,12-Diacetoxy-bisnor-cholanyldiphenylethylene Org. Synth. Coll. Vol. 3, p. 237; Vol. 24, p. 41 · Riegel et al.
  22. Diacetyl-d-tartaric anhydride Org. Synth. Coll. Vol. 4, p. 242; Vol. 35, p. 49 · Shriner and Furrow
  23. Dialkoxyacetylenes: di-tert-butoxyethyne, a valuable synthetic intermediate Org. Synth. Coll. Vol. 8, p. 161; Vol. 65, p. 68 · Bou et al.
  24. Dialkyl mesoxalates by ozonolysis of dialkyl benzalmalonates: dimethyl mesoxalateOxidation Org. Synth. Coll. Vol. 9, p. 314; Vol. 71, p. 214 · Tietze and Bratz