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.

1,705–1,728 of 3,374

  1. Enantioselective oxidation of a sulfide: (S)-(−)-methyl p-tolyl sulfoxideOxidation Org. Synth. Coll. Vol. 8, p. 464; Vol. 68, p. 49 · Zhao et al.
  2. Enantioselective oxidation of an alkyl aryl sulfide: synthesis of (S)-(-)-methyl P-bromophenyl sulfoxideOxidation Org. Synth. Vol. 86, p. 121 · Drago et al.
  3. Enantioselective Preparation of (S)-5-Oxo-5,6-dihydro-2H-pyran-2-yl Benzoate Org. Synth. Vol. 91, p. 293 · Benkovics et al.
  4. Enantioselective preparation of dihydropyrimidones Org. Synth. Vol. 86, p. 236 · Goss et al.
  5. Enantioselective Rhodium-Catalyzed [2+2+2] Cycloaddition of Pentenyl Isocyanate and 4-Ethynylanisole: Preparation and Use of Taddol-pyrrolidine PhosphoramiditeCycloaddition Org. Synth. Vol. 91, p. 150 · Oberg et al.
  6. Enantioselective saponification with pig liver esterase (PLE): (1S,2S,3R)-3-hydroxy-2-nitrocyclohexyl acetate (1,3-Cyclohexanediol, 2-nitro-, 1-acetate, [1S-(1α, 2β, 3α]) Org. Synth. Coll. Vol. 8, p. 332; Vol. 69, p. 19 · Eberle et al.
  7. Enantioselective Synthesis of α- and β- Boc-protected 6-Hydroxy-pyranones: Carbohydrate Building Blocks Org. Synth. Vol. 91, p. 338 · Bajaj et al.
  8. Enantioselective three-component reaction for the preparation of ß-amino-a-hydroxy esters Org. Synth. Vol. 88, p. 418 · Zhou et al.
  9. Enantioselective, catalytic Diels-Alder reaction: (1S-endo)-3-(bicyclo[2.2.1]hept-5-en-2-ylcarbonyl)-2-oxazolidinone (2-Oxazolidinone, 3-bicyclo[2.2.1]hept-5-en-2-ylcarbonyl)-, (1S-endo)-) Org. Synth. Coll. Vol. 9, p. 67; Vol. 71, p. 30 · Pikul and Corey
  10. Endocyclic enamine synthesis: N-methyl-2-phenyl-Δ2-tetrahydropyridine Org. Synth. Coll. Vol. 6, p. 818; Vol. 54, p. 93 · Evans and Domeier
  11. Enol ethers by methylenation of esters: 1-phenoxy-1-phenylethene and 3,4-dihydro-2-methylene-2H-1-benzopyran Org. Synth. Coll. Vol. 8, p. 512; Vol. 69, p. 72 · Pine et al.
  12. Enone reduction-enolate alkylation sequence: 2-allyl-3-methylcyclohexanoneReduction Org. Synth. Coll. Vol. 6, p. 51; Vol. 56, p. 52 · Caine et al.
  13. Epichlorohydrin Org. Synth. Coll. Vol. 1, p. 233; Vol. 3, p. 47 · Clarke and Hartman
  14. Epichlorohydrin and epibromohydrin Org. Synth. Coll. Vol. 2, p. 256; Vol. 16, p. 30 · Braun
  15. Epoxidation of olefins by hydrogen peroxide-acetonitrile: cis-cyclooctene oxideOxidation Org. Synth. Coll. Vol. 7, p. 126; Vol. 60, p. 63 · Bach and Knight
  16. Erucic acidHydrolysis Org. Synth. Coll. Vol. 2, p. 258; Vol. 10, p. 44 · Noller and Talbot
  17. Esterification of carboxylic acids with dicyclohexylcarbodiimide/4-dimethylaminopyridine: tert-butyl ethyl fumarate Org. Synth. Coll. Vol. 7, p. 93; Vol. 63, p. 183 · Neises and Steglich
  18. Esterification of carboxylic acids with trialkyloxonium salts: ethyl and methyl 4-acetoxybenzoates Org. Synth. Coll. Vol. 6, p. 576; Vol. 56, p. 59 · Raber et al.
  19. Esterification of hindered alcohols: tert-butyl p-toluate Org. Synth. Coll. Vol. 6, p. 259; Vol. 51, p. 96 · Crowther et al.
  20. Ethanedithiol Org. Synth. Coll. Vol. 4, p. 401; Vol. 30, p. 35 · Speziale
  21. 1-Ethoxy-1-butyne Org. Synth. Coll. Vol. 6, p. 564; Vol. 57, p. 65 · Newman and Stalick
  22. 3-Ethoxy-2-cyclohexenone Org. Synth. Coll. Vol. 5, p. 539; Vol. 40, p. 41 · Gannon and House
  23. Ethoxyacetic acid and ethyl ethoxyacetate Org. Synth. Coll. Vol. 2, p. 260; Vol. 13, p. 42 · Fuson and Wojcik
  24. Ethoxyacetylene Org. Synth. Coll. Vol. 4, p. 404; Vol. 34, p. 46 · Jones et al.