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.

2,473–2,496 of 3,374

  1. 4-Nonylbenzoic acid Org. Synth. Vol. 81, p. 33 · Fürstner et al.
  2. nor-desoxycholic acid Org. Synth. Coll. Vol. 3, p. 234; Vol. 24, p. 38 · Riegel et al.
  3. 2-Norbornanone Org. Synth. Coll. Vol. 5, p. 852; Vol. 42, p. 79 · Kleinfelter and Schleyer
  4. Norbornylene Org. Synth. Coll. Vol. 4, p. 738; Vol. 37, p. 65 · Meinwald and Hudak
  5. Norcarane Org. Synth. Coll. Vol. 5, p. 855; Vol. 41, p. 72 · Smith and Simmons
  6. Nortricyclanol Org. Synth. Coll. Vol. 5, p. 863; Vol. 45, p. 74 · Meinwald et al.
  7. Nortricyclanone Org. Synth. Coll. Vol. 5, p. 866; Vol. 45, p. 77 · Meinwald et al.
  8. Nucleophilic acylation with disodium tetracarbonylferrate: methyl 7-oxoheptanoate and methyl 7-oxoöctanoate Org. Synth. Coll. Vol. 6, p. 807; Vol. 59, p. 102 · Finke and Sorrell
  9. Nucleophilic aromatic substitution of aryl fluorides by secondary nitriles: preparation of 2-(2-methoxyphenyl)-2-methylpropionitrileSubstitution Org. Synth. Vol. 79, p. 209 · Caron et al.
  10. Nucleophilic hydroxymethylation by the (isopropoxydimethylsilyl)methyl Grignard reagent: 1-(hydroxymethyl)cyclohexanol from cyclohexanoneOrganometallic addition Org. Synth. Coll. Vol. 8, p. 315; Vol. 69, p. 96 · Tamao et al.
  11. Nucleophilic α-sec-aminoalkylation: 2-(diphenylhydroxymethyl)pyrrolidine Org. Synth. Coll. Vol. 6, p. 542; Vol. 58, p. 113 · Enders et al.
  12. Δ9,10-Octalin Org. Synth. Coll. Vol. 6, p. 852; Vol. 50, p. 88 · Kaiser and Benkeser
  13. Δ1(9)-Octalone-2 Org. Synth. Coll. Vol. 5, p. 869; Vol. 45, p. 80 · Augustine and Caputo
  14. 2,2,7,7,12,12,17,17-Octamethyl-21,22,23,24-tetraoxaperhydroquaterene Org. Synth. Coll. Vol. 6, p. 856; Vol. 57, p. 74 · Chastrette et al.
  15. Octanal Org. Synth. Coll. Vol. 5, p. 872; Vol. 47, p. 96 · Franzen
  16. Oleoyl chloride Org. Synth. Coll. Vol. 4, p. 739; Vol. 37, p. 66 · Allen et al.
  17. Oleyl alcohol Org. Synth. Coll. Vol. 2, p. 468; Vol. 15, p. 51 · Reid et al.
  18. Oleyl alcohol Org. Synth. Coll. Vol. 3, p. 671; Vol. 29, p. 80 · Adkins and Gillespie
  19. One-carbon ring expansion of cycloalkanones to conjugated cycloalkenones: 2-cyclohepten-1-one Org. Synth. Coll. Vol. 6, p. 327; Vol. 59, p. 113 · Ito et al.
  20. One-flask synthesis of methyl arylvinyldiazoacetates and their application in enantioselective C-H functionalization: synthesis of (E)-methyl 2-diazo-4-phenylbut-3-enoate and (S,E)-methyl 2-((R)-4-methyl-1,2-dihydronaphthalen-2-yl)-4-phenylbut-3-enoate Org. Synth. Vol. 84, p. 334 · Manning and Davies
  21. One-pot conversion of lactam carbamates to cyclic enecarbamates: preparation of 1-tert-butoxycarbonyl-2,3-dihydropyrrole Org. Synth. Vol. 85, p. 64 · Yu* et al.
  22. One-pot diazotization and Heck reaction of methyl anthranilate: 2-(3-oxopropyl)benzoic acid methyl esterCross-coupling Org. Synth. Vol. 87, p. 226 · Zaragoza
  23. One-pot multicomponent preparation of tetrahydropyrazoloquinolinones and tetrahydropyrazoloquinazolinones Org. Synth. Vol. 86, p. 252 · Glasnov and Kappe
  24. One-pot Preparation of (S)-N-[(S)-1-Hydroxy-4-methyl-1,1-diphenylpentan-2-yl]pyrrolidine-2-carboxamide from L-Proline Org. Synth. Vol. 91, p. 137 · Harnying et al.