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.

1,849–1,872 of 2,861

  1. Naphthalene-1,5-disulfonyl chloride Org. Synth. Coll. Vol. 4, p. 693; Vol. 32, p. 88 · Caesar
  2. 2,3-Naphthalenedicarboxylic acid Org. Synth. Coll. Vol. 5, p. 810; Vol. 43, p. 80 · Friedman
  3. 2,6-Naphthalenedicarboxylic acid Org. Synth. Coll. Vol. 5, p. 813; Vol. 40, p. 71 · Raecke and Schirp
  4. 1,5-Naphthalenedithiol Org. Synth. Coll. Vol. 4, p. 695; Vol. 33, p. 47 · Caesar
  5. 1,2-Naphthalic anhydride Org. Synth. Coll. Vol. 2, p. 423; Vol. 18, p. 59 · Hershberg and Fieser
  6. α-Naphthoic acid Org. Synth. Coll. Vol. 2, p. 425; Vol. 11, p. 80 · Gilman et al.
  7. β-Naphthoic acid Org. Synth. Coll. Vol. 2, p. 428; Vol. 17, p. 65 · Newman and Holmes
  8. β-Naphthol phenylaminomethane Org. Synth. Coll. Vol. 1, p. 381; Vol. 9, p. 60 · Betti
  9. α-Naphthonitrile Org. Synth. Coll. Vol. 3, p. 631; Vol. 21, p. 89 · Newman
  10. 1,4-Naphthoquinone Org. Synth. Coll. Vol. 1, p. 383; Vol. 5, p. 79 · Fieser
  11. 1,2-Naphthoquinone Org. Synth. Coll. Vol. 2, p. 430; Vol. 17, p. 68 · Fieser
  12. 1,4-Naphthoquinone Org. Synth. Coll. Vol. 4, p. 698; Vol. 33, p. 50 · Braude and Fawcett
  13. 1,2-Naphthoquinone-4-sulfonate, ammonium and potassium Org. Synth. Coll. Vol. 3, p. 633; Vol. 21, p. 91 · Martin and Fieser
  14. Naphthoresorcinol Org. Synth. Coll. Vol. 3, p. 637; Vol. 25, p. 73 · Meyer and Bloch
  15. α-Naphthyl isothiocyanate Org. Synth. Coll. Vol. 4, p. 700; Vol. 36, p. 56 · Cymerman-Craig et al.
  16. (S)-(−)-α-(1-Naphthyl)ethylamine Org. Synth. Coll. Vol. 6, p. 826; Vol. 55, p. 80 · Mohacsi and Leimgruber
  17. β-Naphthylmercuric chloride Org. Synth. Coll. Vol. 2, p. 432; Vol. 12, p. 54 · Nesmajanow
  18. N-β-Naphthylpiperidine Org. Synth. Coll. Vol. 5, p. 816; Vol. 40, p. 74 · Bunnett et al.
  19. (S)-(+)-Neomenthyldiphenylphosphine in nickel-catalyzed asymmetric reductive coupling of alkynes and aldehydes: enantioselective synthesis of allylic alcohols and α-hydroxy ketonesCross-coupling Org. Synth. Vol. 84, p. 111 · Dyke et al.
  20. Neopentyl alcohol Org. Synth. Coll. Vol. 5, p. 818; Vol. 40, p. 76 · Hoffman
  21. Neophyl chloride Org. Synth. Coll. Vol. 4, p. 702; Vol. 32, p. 90 · Smith and Sellas
  22. A new practical one-pot conversion of phenols to anilines: 6-amino-3,4-dihydro-1(2H)-naphthalenone Org. Synth. Vol. 84, p. 325 · Mizuno and Yamano
  23. A new reagent for tert-butoxycarbonylation: 2-tert-butoxycarbonyloxyimino-2-phenylacetonitrile Org. Synth. Coll. Vol. 6, p. 199; Vol. 59, p. 95 · Itoh et al.
  24. New, convenient route for trifluoromethylation of steroidal molecules Org. Synth. Vol. 87, p. 126 · Fei et al.