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.

1,609–1,632 of 2,861

  1. 4-Ketoundecanoic acid Org. Synth. Coll. Vol. 9, p. 530; Vol. 73, p. 215 · Tschantz et al.
  2. Kryptopyrrole Org. Synth. Coll. Vol. 3, p. 513; Vol. 21, p. 67 · Fischer
  3. Lactamide Org. Synth. Coll. Vol. 3, p. 516; Vol. 21, p. 71 · Kleinberg and Audrieth
  4. 18,20-Lactone of 3β-acetoxy-20β-hydroxy-5-pregnene-18-oic acid Org. Synth. Coll. Vol. 5, p. 692; Vol. 45, p. 57 · Heusler et al.
  5. Large scale, green synthesis of a generation-1 melamine (triazine) dendrimer Org. Synth. Vol. 86, p. 151 · Chouai et al.
  6. Laurone Org. Synth. Coll. Vol. 4, p. 560; Vol. 31, p. 68 · Sauer
  7. Lauryl alcohol Org. Synth. Coll. Vol. 2, p. 372; Vol. 10, p. 62 · Ford and Marvel
  8. Laurylmethylamine Org. Synth. Coll. Vol. 4, p. 564; Vol. 36, p. 48 · Wilson and Stenberg
  9. Lepidine Org. Synth. Coll. Vol. 3, p. 519; Vol. 26, p. 45 · Neumann et al.
  10. Levopimaric acid Org. Synth. Coll. Vol. 5, p. 699; Vol. 45, p. 64 · Lloyd and Hedrick
  11. Levulinic acid Org. Synth. Coll. Vol. 1, p. 335; Vol. 9, p. 50 · McKenzie
  12. Ligand-free copper(II) oxide nanoparticles catalyzed synthesis of substituted benzoxazoles Org. Synth. Vol. 88, p. 398 · Saha et al.
  13. Linoleic acid Org. Synth. Coll. Vol. 3, p. 526; Vol. 22, p. 75 · McCutcheon
  14. Linolenic acid Org. Synth. Coll. Vol. 3, p. 531; Vol. 22, p. 82 · McCutcheon
  15. Lipase-catalyzed kinetic resolution of alcohols via chloroacetate esters: (−)-(1R,2S)-trans-2-phenylcyclohexanol and (+)-(1S,2R)-trans-2-phenylcyclohexanol Org. Synth. Coll. Vol. 8, p. 516; Vol. 69, p. 1 · Schwartz et al.
  16. Lipase-catalyzed resolution of 4-trimethylsilyl-3-butyn-2-ol and conversion of the (R)-enantiomer to (R)-3-butyn-2-yl mesylate and (P)-1-tributylstannyl-1,2-butadiene Org. Synth. Vol. 82, p. 43 · Marshall and Chobanian
  17. Lithiated primary alkyl carbamates for the homologation of boronic esters Org. Synth. Vol. 88, p. 247 · Webster et al.
  18. Lithium amides as homochiral ammonia equivalents for conjugate additions to α,β-unsaturated esters: asymmetric synthesis of (S)-β-leucineAddition Org. Synth. Vol. 87, p. 143 · Davies et al.
  19. Low pressure carbonylation of epoxides to β-lactones Org. Synth. Vol. 86, p. 287 · Kramer et al.
  20. Low-epimerization Peptide Bond Formation with Oxyma Pure: Preparation of Z-L-Phg-Val-OMe Org. Synth. Vol. 90, p. 306 · Subirós-Funosas and Albericio.*
  21. Macrocyclic diimines: 1,10-diazacycloöctadecane Org. Synth. Coll. Vol. 6, p. 382; Vol. 54, p. 88 · Park and Simmons
  22. Macrocyclic polyamines: 1,4,7,10,13,16-hexaäzacycloöctadecane Org. Synth. Coll. Vol. 6, p. 652; Vol. 58, p. 86 · Atkins et al.
  23. Macrocyclic polyethers: dibenzo-18-crown-6 polyether and dicyclohexyl-18-crown-6 polyether Org. Synth. Coll. Vol. 6, p. 395; Vol. 52, p. 66 · Pedersen
  24. Macrolides from cyclization of ω-bromocarboxylic acids: 11-hydroxyundecanoic lactoneCyclization Org. Synth. Coll. Vol. 6, p. 698; Vol. 58, p. 98 · Galli and Mandolini