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.

1,081–1,104 of 2,861

  1. β,β-Diphenylpropiophenone Org. Synth. Coll. Vol. 2, p. 236; Vol. 17, p. 51 · Shildneck
  2. 2,4-Diphenylpyrrole Org. Synth. Coll. Vol. 3, p. 358; Vol. 27, p. 33 · Allen and Wilson
  3. Diphenylselenium dichloride and triphenylselenonium chloride Org. Synth. Coll. Vol. 2, p. 240; Vol. 18, p. 30 · Leicester
  4. 2,3-Diphenylsuccinonitrile Org. Synth. Coll. Vol. 4, p. 392; Vol. 32, p. 63 · Davis and Ward
  5. 2,3-Diphenylvinylene sulfone Org. Synth. Coll. Vol. 6, p. 555; Vol. 50, p. 65 · Carpino and III
  6. Direct chlorination of alcohols: synthesis of ethyl 3-chloro-3-phenylpropanoate Org. Synth. Vol. 83, p. 38 · Yasuda et al.
  7. Direct Conversion of Benzylic and Allylic Alcohols to Diethyl Phosphonates Org. Synth. Vol. 90, p. 145 · Richardson and Wiemer
  8. Direct degradation of the biopolymer poly[(R)-3-hydroxybutyric acid] to (R)-3-hydroxybutanoic acid and its methyl ester Org. Synth. Coll. Vol. 9, p. 483; Vol. 71, p. 39 · Seebach et al.
  9. Direct fluorination of the carbonyl group of benzophenones using deoxo-fluor®: preparation of bis(4-fluorophenyl)difluoromethane Org. Synth. Vol. 87, p. 245 · Chang et al.
  10. Direct iodination of polyalkylbenzenes: iododurene Org. Synth. Coll. Vol. 6, p. 700; Vol. 51, p. 94 · Suzuki
  11. Direct nucleophilic acylation by the low-temperature, in situ generation of acyllithium reagents; α-hydroxy ketones from ketones: 3-hydroxy-2,2,3-trimethyloctan-4-one from pinacoloneRearrangement Org. Synth. Coll. Vol. 8, p. 343; Vol. 69, p. 114 · Hui and Seyferth
  12. Direct synthesis of 2,5-dihalosiloles Org. Synth. Vol. 85, p. 53 · Morra and Pagenkopf
  13. Direct Synthesis of Azaheterocycles from N-Aryl/Vinyl Amides. Synthesis of 4-(Methylthio)-2-phenylquinazoline and 4-(4-Methoxyphenyl)-2-phenylquinoline Org. Synth. Vol. 89, p. 549 · Ahmad et al.
  14. Directed aldol condensations: threo-4-hydroxy-3-phenyl-2-heptanoneCondensation Org. Synth. Coll. Vol. 6, p. 692; Vol. 54, p. 49 · Auerbach et al.
  15. Directed aldol condensations: β-phenylcinnamaldehydeCondensation Org. Synth. Coll. Vol. 6, p. 901; Vol. 50, p. 66 · Wittig and Hesse
  16. Directed homogeneous hydrogenation: methyl anti-3-hydroxy-2-methylpentanoateReduction Org. Synth. Coll. Vol. 8, p. 420; Vol. 68, p. 64 · Brown et al.
  17. Directed lithiation of aromatic compounds: (2-dimethylamino-5-methylphenyl)diphenylcarbinol Org. Synth. Coll. Vol. 6, p. 478; Vol. 53, p. 56 · Hay and Harris
  18. erythro-Directed reduction of a β-keto amide: erythro-1-(3-hydroxy-2-methyl-3-phenylpropanoyl)piperidineReduction Org. Synth. Coll. Vol. 8, p. 326; Vol. 69, p. 44 · Fujita and Hiyama
  19. Discussion Addendum for: Org. Synth. Vol. 89, p. 307 · Obora* and Ishii*
  20. Discussion Addendum for:Oxidation Org. Synth. Vol. 89, p. 311 · Leonellia et al.
  21. Discussion Addendum for: Org. Synth. Vol. 89, p. 323 · Dondoni* and Marra
  22. Discussion Addendum for: Org. Synth. Vol. 89, p. 334 · Meijere* and Kozhushkov
  23. Discussion Addendum for:Oxidation Org. Synth. Vol. 89, p. 350 · Ramirez et al.
  24. Discussion Addendum for: Org. Synth. Vol. 89, p. 374 · Sato et al.