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.

1,129–1,152 of 3,374

  1. Cholestenone Org. Synth. Coll. Vol. 3, p. 207; Vol. 21, p. 18 · Oppenauer
  2. Cholesterol, Δ5-cholesten-3-one, and Δ4-cholesten-3-one Org. Synth. Coll. Vol. 4, p. 195; Vol. 35, p. 43 · Fieser
  3. Cinnamonitrile Org. Synth. Coll. Vol. 6, p. 304; Vol. 50, p. 18 · Lohaus
  4. Cinnamyl bromide Org. Synth. Coll. Vol. 5, p. 249; Vol. 48, p. 51 · Schaefer et al.
  5. Citraconic anhydride and citraconic acid Org. Synth. Coll. Vol. 2, p. 140; Vol. 11, p. 28 · Shriner et al.
  6. Cleavage of methyl ethers with iodotrimethylsilane: cyclohexanol from cyclohexyl methyl ether Org. Synth. Coll. Vol. 6, p. 353; Vol. 59, p. 35 · Jung and Lyster
  7. Condensation of (−)-dimenthyl succinate dianion with 1,ω-dihalides: (+)-(1S,2S)-cyclopropane-1,2-dicarboxylic acidCondensation Org. Synth. Coll. Vol. 8, p. 141; Vol. 67, p. 76 · Furuta et al.
  8. Condensation of dimethyl 1,3-acetonedicarboxylate with 1,2-dicarbonyl compounds: cis-bicyclo[3.3.0]octane-3,7-dionesCondensation Org. Synth. Coll. Vol. 7, p. 50; Vol. 64, p. 27 · Bertz et al.
  9. Conjugate addition of a vinylzirconium reagent: 3-(1-octen-1-yl)cyclopentanoneAddition Org. Synth. Coll. Vol. 9, p. 640; Vol. 71, p. 83 · Sun et al.
  10. Conjugate addition–cyclization of a cyanocuprate: 2-carbomethoxy-3-vinylcyclopentanoneCyclization Org. Synth. Coll. Vol. 8, p. 112; Vol. 66, p. 52 · Nugent and Hobbs
  11. Conjugate allylation of α,β-unsaturated ketones with allylsilanes: 4-phenyl-6-hepten-2-one Org. Synth. Coll. Vol. 7, p. 443; Vol. 62, p. 86 · Sakurai et al.
  12. Conjugate reduction of α,β-unsaturated p-toluenesulfonylhydrazones to alkenes with catecholborane: 5β-cholest-3-eneReduction Org. Synth. Coll. Vol. 6, p. 293; Vol. 59, p. 42 · Kabalka et al.
  13. Controlled-potential electrolytic reduction: 1,1-bis(bromomethyl)cyclopropaneReduction Org. Synth. Coll. Vol. 6, p. 153; Vol. 52, p. 22 · Rifi
  14. Convenient preparation of 3-ethoxycarbonyl benzofurans from salicylaldehydes and ethyl diazoacetate Org. Synth. Vol. 86, p. 172 · Dudley et al.
  15. A convenient preparation of an orthogonally protected Cα,Cα-disubstituted amino acid analog of lysine: 1-tert-butyloxycarbonyl-4-((9-fluorenylmethyloxycarbonyl)amino)-piperidine-4-carboxylic acid Org. Synth. Vol. 81, p. 213 · Hammarström et al.
  16. Convenient Synthesis of α-Diazoacetates from α-Bromoacetates and N,N'-Ditosylhydrazine: Preparation of Benzyl Diazoacetate Org. Synth. Vol. 89, p. 501 · Ideue et al.
  17. Conversion of amines to phospho esters: decyl diethyl phosphate Org. Synth. Coll. Vol. 9, p. 194; Vol. 72, p. 246 · Nikolaides et al.
  18. Conversion of arylalkylketones into dichloroalkenes: (1-chloro-4-(2,2-dichloro-1-methylethenyl)-benzene) Org. Synth. Vol. 82, p. 93 · Nenajdenko et al.
  19. Conversion of epoxides to β-hydroxy isocyanides: trans-2-isocyanocyclohexanol Org. Synth. Coll. Vol. 7, p. 294; Vol. 64, p. 39 · Gassman and Guggenheim
  20. Conversion of esters to allylsilanes: trimethyl(2-methylene-4-phenyl-3-butenyl)silane Org. Synth. Coll. Vol. 8, p. 602; Vol. 69, p. 89 · Bunnelle and Narayanan
  21. Conversion of esters to amides with dimethylaluminum amides: N,N-dimethylcyclohexanecarboxamide Org. Synth. Coll. Vol. 6, p. 492; Vol. 59, p. 49 · Lipton et al.
  22. Conversion of ketones to cyanohydrins: benzophenone cyanohydrin Org. Synth. Coll. Vol. 7, p. 20; Vol. 60, p. 14 · Gassman and Talley
  23. Conversion of methyl ketones into terminal acetylenes: ethynylferrocene Org. Synth. Coll. Vol. 9, p. 411; Vol. 73, p. 262 · Polin and Schottenberger
  24. Conversion of methyl ketones into terminal alkynes: (E)-buten-3-ynyl-2,6,6-trimethyl-1-cyclohexene Org. Synth. Coll. Vol. 7, p. 63; Vol. 64, p. 44 · Negishi et al.