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.

1,537–1,560 of 2,861

  1. Intermolecular retro-Cope Type Hydroxylamination of Alkynes with NH2OH: E-1-(1-Hydroxycyclohexyl)ethanone oximeRearrangement Org. Synth. Vol. 90, p. 87 · Loiseau and Beauchemin
  2. Intra- and intermolecular Kulinkovich cyclopropanation reactions of carboxylic esters with olefins: bicyclo[3.1.0]hexan-1-ol and trans-2-benzyl-1-methylcyclopropan-1-ol Org. Synth. Vol. 80, p. 111 · Kim et al.
  3. Intramolecular cyclization of cis,cis-1,5-cyclooctadiene using hypervalent iodine: bicyclo[3.3.0]octane-2,6-dioneCyclization Org. Synth. Coll. Vol. 8, p. 43; Vol. 68, p. 175 · Moriarty et al.
  4. Intramolecular oxidative coupling of a bisenolate: 4-methyltricyclo[2.2.2.03,5]octane-2,6-dioneCross-coupling Org. Synth. Coll. Vol. 8, p. 467; Vol. 69, p. 173 · Poupart et al.
  5. Inverse electron-demand Diels-Alder cycloaddition of a ketene dithioacetal. Copper hydride-promoted reduction of a conjugated enone. 9-Dithiolanobicyclo[3.2.2]non-6-en-2-one from troponeCycloaddition Org. Synth. Coll. Vol. 9, p. 396; Vol. 71, p. 181 · Dahnke and Paquette
  6. 2-Iodo-p-xylene Org. Synth. Coll. Vol. 6, p. 709; Vol. 55, p. 70 · Taylor et al.
  7. p-Iodoaniline Org. Synth. Coll. Vol. 2, p. 347; Vol. 11, p. 62 · Brewster
  8. 5-Iodoanthranilic acid Org. Synth. Coll. Vol. 2, p. 349; Vol. 19, p. 52 · Wallingford and Krueger
  9. Iodobenzene Org. Synth. Coll. Vol. 1, p. 323; Vol. 9, p. 46 · Dains and Brewster
  10. Iodobenzene Org. Synth. Coll. Vol. 2, p. 351; Vol. 19, p. 55 · Lucas and Kennedy
  11. Iodobenzene dichloride Org. Synth. Coll. Vol. 3, p. 482; Vol. 22, p. 69 · Lucas and Kennedy
  12. p-Iodobenzoic acid Org. Synth. Coll. Vol. 1, p. 325; Vol. 7, p. 58 · Whitmore and Woodward
  13. m-Iodobenzoic acid Org. Synth. Coll. Vol. 2, p. 353; Vol. 19, p. 57 · Wallingford and Krueger
  14. Iodocyclohexane Org. Synth. Coll. Vol. 4, p. 543; Vol. 31, p. 66 · Stone and Shechter
  15. Z-1-Iodohexene Org. Synth. Coll. Vol. 7, p. 290; Vol. 62, p. 1 · Alexakis et al.
  16. Iodolactamization: 8-exo-iodo-2-azabicyclo[3.3.0]octan-3-one Org. Synth. Coll. Vol. 9, p. 516; Vol. 70, p. 101 · Knapp and Gibson
  17. o-Iodophenol Org. Synth. Coll. Vol. 1, p. 326; Vol. 4, p. 37 · Whitmore and Hanson
  18. p-Iodophenol Org. Synth. Coll. Vol. 2, p. 355; Vol. 15, p. 39 · Dains and Eberly
  19. trans-Iodopropenylation of alkyl halides: (E)-1-iodo-4-phenyl-2-butene Org. Synth. Coll. Vol. 6, p. 704; Vol. 56, p. 77 · Hirai and Kishida
  20. Iodosobenzene Org. Synth. Coll. Vol. 3, p. 483; Vol. 22, p. 70 · Lucas et al.
  21. Iodosobenzene Org. Synth. Coll. Vol. 5, p. 658; Vol. 43, p. 60 · Saltzman and Sharefkin
  22. Iodosobenzene diacetate Org. Synth. Coll. Vol. 5, p. 660; Vol. 43, p. 62 · Sharefkin and Saltzman
  23. N-Iodosuccinimide Org. Synth. Coll. Vol. 5, p. 663; Vol. 42, p. 73 · Benson et al.
  24. 2-Iodothiophene Org. Synth. Coll. Vol. 2, p. 357; Vol. 12, p. 44 · Minnis