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.

2,065–2,088 of 2,861

  1. 4-Pentyn-1-ol Org. Synth. Coll. Vol. 4, p. 755; Vol. 33, p. 68 · Jones et al.
  2. Peptide syntheses using N-ethyl-5-phenylisoxazolium-3'-sulfonate: carbobenzoxy-L-asparaginyl-L-leucine methyl ester and N-carbobenzoxy-3-hydroxy-L-prolylglycylglycine ethyl ester Org. Synth. Coll. Vol. 6, p. 263; Vol. 56, p. 88 · Woodward and Olofson
  3. Peptide synthesis using 1-(4-chlorophenyl)-3-(4'-methyl-1'-piperazinyl)-2-propyn-1-one as reagent: benzyloxycarbonyl-L-alanyl-L-cysteine methyl ester and benzyloxycarbonyl-L-aspartyl-(tert-butyl ester)-L-phenylalanyl-L-valine methyl ester Org. Synth. Coll. Vol. 7, p. 30; Vol. 63, p. 175 · Fahrni et al.
  4. Perbenzoic acid Org. Synth. Coll. Vol. 1, p. 431; Vol. 8, p. 30 · Braun
  5. Perchlorofulvalene Org. Synth. Coll. Vol. 5, p. 901; Vol. 46, p. 93 · Mark
  6. Perhydro-9b-boraphenalene and perhydro-9b-phenalenol Org. Synth. Coll. Vol. 7, p. 427; Vol. 61, p. 103 · Negishi and Brown
  7. Peroxybenzoic acid Org. Synth. Coll. Vol. 5, p. 904; Vol. 44, p. 81 · Silbert et al.
  8. Phase-transfer alkylation of nitriles: 2-phenylbutyronitrile Org. Synth. Coll. Vol. 6, p. 897; Vol. 55, p. 91 · Makosza and Jonczyk
  9. Phase-transfer Hofmann carbylamine reaction: tert-butyl isocyanideRearrangement Org. Synth. Coll. Vol. 6, p. 232; Vol. 55, p. 96 · Gokel et al.
  10. Phenacyl bromide Org. Synth. Coll. Vol. 2, p. 480; Vol. 19, p. 24 · Cowper and Davidson
  11. Phenacylamine hydrochloride Org. Synth. Coll. Vol. 5, p. 909; Vol. 41, p. 82 · Baumgarten and Petersen
  12. Phenanthrene-9-aldehyde Org. Synth. Coll. Vol. 3, p. 701; Vol. 28, p. 83 · Dornfeld and Coleman
  13. Phenanthrenequinone Org. Synth. Coll. Vol. 4, p. 757; Vol. 34, p. 76 · Wendland and LaLonde
  14. Phenols: 6-methoxy-2-naphthol Org. Synth. Coll. Vol. 5, p. 918; Vol. 49, p. 90 · Kidwell et al.
  15. Phenoxthin Org. Synth. Coll. Vol. 2, p. 485; Vol. 18, p. 64 · Suter and Maxwell
  16. γ-Phenoxypropyl bromide Org. Synth. Coll. Vol. 1, p. 435; Vol. 9, p. 72 · Marvel and Tanenbaum
  17. Phenyl azide Org. Synth. Coll. Vol. 3, p. 710; Vol. 22, p. 96 · Lindsay and Allen
  18. Phenyl cinnamate Org. Synth. Coll. Vol. 3, p. 714; Vol. 20, p. 77 · Womack and McWhirter
  19. Phenyl isothiocyanate Org. Synth. Coll. Vol. 1, p. 447; Vol. 6, p. 72 · Dains et al.
  20. Phenyl t-butyl ether Org. Synth. Coll. Vol. 5, p. 924; Vol. 45, p. 89 · Frisell and Lawesson
  21. Phenyl t-butyl ether Org. Synth. Coll. Vol. 5, p. 926; Vol. 41, p. 91 · Sahyun and Cram
  22. Phenyl thienyl ketone Org. Synth. Coll. Vol. 2, p. 520; Vol. 12, p. 62 · Minnis
  23. Phenyl vinyl sulfide Org. Synth. Coll. Vol. 9, p. 662; Vol. 74, p. 124 · Reno and Pariza
  24. Phenyl vinyl sulfone and sulfoxide Org. Synth. Coll. Vol. 7, p. 453; Vol. 64, p. 157 · Paquette and Carr