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.

577–600 of 3,374

  1. Acylamidoalkyl acetophenones from substituted phenethylamines: 2-(2-acetamidoethyl)-4,5-dimethoxyacetophenone Org. Synth. Coll. Vol. 6, p. 1; Vol. 56, p. 3 · Brossi et al.
  2. 1-N-Acylamino-1,3-dienes from 2,4-pentadienoic acids by the Curtius rearrangement: benzyl trans-1,3-butadiene-1-carbamateRearrangement Org. Synth. Coll. Vol. 6, p. 95; Vol. 59, p. 1 · Jessup et al.
  3. Acyloin condensation by thiazolium ion catalysis: butyroinCondensation Org. Synth. Coll. Vol. 7, p. 95; Vol. 62, p. 170 · Stetter and Kuhlmann
  4. Acyloin condensation in which chlorotrimethylsilane is used as a trapping agent: 1,2-bis(trimethylsilyloxy)cyclobutene and 2-hydroxycyclobutanoneCondensation Org. Synth. Coll. Vol. 6, p. 167; Vol. 57, p. 1 · Bloomfield and Nelke
  5. Adamantane Org. Synth. Coll. Vol. 5, p. 16; Vol. 42, p. 8 · Schleyer et al.
  6. 2-Adamantanecarbonitrile Org. Synth. Coll. Vol. 6, p. 41; Vol. 57, p. 8 · Oldenziel et al.
  7. 1-Adamantanecarboxylic acid Org. Synth. Coll. Vol. 5, p. 20; Vol. 44, p. 1 · Koch and Haaf
  8. Adamantanone Org. Synth. Coll. Vol. 6, p. 48; Vol. 53, p. 8 · Geluk and Keizer
  9. 1,2-Addition of a functionalized zinc-copper organometallic [RCu(CN)ZnI] to an α,β-unsaturated aldehyde: (E)-2-(4-hydroxy-6-phenyl-5-hexenyl)-1H-isoindole-1,3(2H)-dioneAddition Org. Synth. Coll. Vol. 9, p. 502; Vol. 70, p. 195 · Yeh et al.
  10. Addition of an ethylcopper complex to 1-octyne: (E)-5-ethyl-1,4-undecadieneAddition Org. Synth. Coll. Vol. 7, p. 236; Vol. 64, p. 1 · Iyer and Helquist
  11. Addition of dialkylamines to myrcene: N,N-diethylgeranylamineAddition Org. Synth. Coll. Vol. 8, p. 188; Vol. 67, p. 44 · Takabe et al.
  12. Addition of organolithium reagents to allyl alcohol: 2-methyl-1-hexanolAddition Org. Synth. Coll. Vol. 6, p. 786; Vol. 55, p. 1 · Crandall and Rojas
  13. Adipic acid Org. Synth. Coll. Vol. 1, p. 18; Vol. 5, p. 9 · Ellis
  14. Air Oxidation of Primary Alcohols Catalyzed by Copper(I)/TEMPO. Preparation of 2-Amino-5-bromobenzaldehydeOxidation Org. Synth. Vol. 90, p. 240 · Hoover and Stahl.
  15. β-Alanine Org. Synth. Coll. Vol. 2, p. 19; Vol. 16, p. 1 · Clarke and Behr
  16. β-Alanine Org. Synth. Coll. Vol. 3, p. 34; Vol. 27, p. 1 · Ford
  17. Aldehydes by oxidation of terminal olefins with chromyl chloride: 2,4,4-trimethylpentanalOxidation Org. Synth. Coll. Vol. 6, p. 1028; Vol. 51, p. 4 · Freeman et al.
  18. Aldehydes from 2-benzyl-4,4,6-trimethyl-5,6-dihydro-1,3(4H)-oxazine: 1-phenylcyclopentanecarboxaldehyde Org. Synth. Coll. Vol. 6, p. 905; Vol. 51, p. 24 · Politzer and Meyers
  19. Aldehydes from 4,4-dimethyl-2-oxazoline and Grignard reagents: o-anisaldehydeOrganometallic addition Org. Synth. Coll. Vol. 6, p. 64; Vol. 54, p. 42 · Brinkmeyer et al.
  20. Aldehydes from acid chlorides by modified Rosenmund reduction: 3,4,5-trimethoxybenzaldehydeReduction Org. Synth. Coll. Vol. 6, p. 1007; Vol. 51, p. 8 · Rachlin et al.
  21. Aldehydes from acid chlorides by reduction of ester-mesylates with sodium borohydride: cyclobutanecarboxaldehydeReduction Org. Synth. Coll. Vol. 6, p. 312; Vol. 51, p. 11 · Johnson and Rickborn
  22. Aldehydes from allylic alcohols and phenylpalladium acetate: 2-methyl-3-phenylpropionaldehyde Org. Synth. Coll. Vol. 6, p. 815; Vol. 51, p. 17 · Heck
  23. Aldehydes from aromatic nitriles: 4-formylbenzenesulfonamide Org. Synth. Coll. Vol. 6, p. 631; Vol. 51, p. 20 · Es and Staskun
  24. Aldehydes from olefins: cyclohexanecarboxaldehyde Org. Synth. Coll. Vol. 6, p. 338; Vol. 57, p. 11 · Pino and Botteghi