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.

625–648 of 3,374

  1. Allantoin Org. Synth. Coll. Vol. 2, p. 21; Vol. 13, p. 1 · Hartman et al.
  2. Allene Org. Synth. Coll. Vol. 5, p. 22; Vol. 42, p. 12 · Cripps and Kiefer
  3. α-Allenic esters from α-phosphoranylidene esters and acid chlorides: ethyl 2,3-pentadienoate Org. Synth. Coll. Vol. 7, p. 232; Vol. 62, p. 202 · Lang and Hansen
  4. Alloxan monohydrate Org. Synth. Coll. Vol. 3, p. 37; Vol. 23, p. 3 · Hartman and Sheppard
  5. Alloxan monohydrate Org. Synth. Coll. Vol. 4, p. 23; Vol. 32, p. 6 · Holmgren and Wenner
  6. Alloxantin dihydrate Org. Synth. Coll. Vol. 3, p. 42; Vol. 23, p. 6 · Nightingale
  7. Alloxantin dihydrate Org. Synth. Coll. Vol. 4, p. 25; Vol. 33, p. 3 · Tipson
  8. Allyl alcohol Org. Synth. Coll. Vol. 1, p. 42; Vol. 1, p. 15 · Kamm and Marvel
  9. Allyl Cyanate-To-Isocyanate Rearrangement: Preparation of tert-Butyl 3,7-dimethylocta-1,6-dien-3-ylcarbamateRearrangement Org. Synth. Vol. 90, p. 271 · Ichikawa et al.
  10. Allyl cyanide Org. Synth. Coll. Vol. 1, p. 46; Vol. 8, p. 4 · Supniewski and Salzberg
  11. Allyl lactate Org. Synth. Coll. Vol. 3, p. 46; Vol. 26, p. 4 · Rehberg
  12. Allylamine Org. Synth. Coll. Vol. 2, p. 24; Vol. 18, p. 5 · Leffler
  13. Allylboronation of imines: 1-phenylhex-5-en-3-amine Org. Synth. Vol. 83, p. 170 · Sugiura et al.
  14. Allylcarbamates by the aza-ene reaction: methyl N-(2-methyl-2-butenyl)carbamate Org. Synth. Coll. Vol. 8, p. 427; Vol. 65, p. 159 · Kresze et al.
  15. 2-Allylcyclohexanone Org. Synth. Coll. Vol. 3, p. 44; Vol. 28, p. 8 · Vanderwerf and Lemmerman
  16. 2-Allylcyclohexanone Org. Synth. Coll. Vol. 5, p. 25; Vol. 42, p. 14 · Howard and Lorette
  17. (S)-(-)-2-Allylcyclohexanone Org. Synth. Vol. 86, p. 47 · Braun et al.
  18. Allylic acetoxylation of cycloalkenes: 2-cyclohepten-1-yl acetate Org. Synth. Coll. Vol. 8, p. 137; Vol. 68, p. 109 · Heumann et al.
  19. Allylic alcohols by alkene transfer from zirconium to zinc: 1-[(tert-butyldiphenylsilyl)oxy]-dec-3-en-5-ol Org. Synth. Coll. Vol. 9, p. 143; Vol. 74, p. 205 · Wipf and Xu
  20. Allylic chlorides from allylic alcohols: geranyl chloride Org. Synth. Coll. Vol. 6, p. 638; Vol. 54, p. 68 · Stork et al.
  21. Allylic Oxidation Catalyzed by Dirhodium(II) Tetrakis[ε-caprolactamate] of tert-Butyldimethylsilyl-protected trans-DehydroandrosteroneOxidation Org. Synth. Vol. 89, p. 19 · Ratnikov* et al.
  22. Allylic oxidation with hydrogen peroxide–selenium dioxide: trans-pinocarveolOxidation Org. Synth. Coll. Vol. 6, p. 946; Vol. 56, p. 25 · Coxon et al.
  23. Allylically transposed amines from allylic alcohols: 3,7-dimethyl-1,6-octadien-3-amine Org. Synth. Coll. Vol. 6, p. 507; Vol. 58, p. 4 · Clizbe and Overman
  24. Allylindation in aqueous media: methyl 3-(hydroxymethyl)-4-methyl-2-methylenepentanoate Org. Synth. Vol. 77, p. 107 · Bennett and Paquette