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.

2,377–2,400 of 3,374

  1. (S)-(−)-α-(1-Naphthyl)ethylamine Org. Synth. Coll. Vol. 6, p. 826; Vol. 55, p. 80 · Mohacsi and Leimgruber
  2. β-Naphthylmercuric chloride Org. Synth. Coll. Vol. 2, p. 432; Vol. 12, p. 54 · Nesmajanow
  3. N-β-Naphthylpiperidine Org. Synth. Coll. Vol. 5, p. 816; Vol. 40, p. 74 · Bunnett et al.
  4. (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.
  5. Neopentyl alcohol Org. Synth. Coll. Vol. 5, p. 818; Vol. 40, p. 76 · Hoffman
  6. Neophyl chloride Org. Synth. Coll. Vol. 4, p. 702; Vol. 32, p. 90 · Smith and Sellas
  7. 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
  8. 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.
  9. New, convenient route for trifluoromethylation of steroidal molecules Org. Synth. Vol. 87, p. 126 · Fei et al.
  10. Ni-catalyzed Reductive Cleavage of Methyl 3-Methoxy-2-Naphthoate Org. Synth. Vol. 91, p. 260 · Cornella et al.
  11. Nickel-catalyzed asymmetric Negishi cross-couplings of racemic secondary allylic chlorides with alkylzincs: (S,E)-ethyl 6-(1,3-dioxolan-2-yl)-4-methylhex-2-enoateCross-coupling Org. Synth. Vol. 87, p. 317 · Lou and Fu
  12. Nickel-catalyzed coupling of aryl O-carbamates with Grignard reagents: 2,7-dimethylnaphthaleneOrganometallic addition Org. Synth. Vol. 78, p. 42 · Dallairea et al.
  13. Nickel-Catalyzed Cross-Coupling of Aryl Halides with Alkyl Halides: Ethyl 4-(4-(4-methylphenylsulfonamido)-phenyl)butanoateCross-coupling Org. Synth. Vol. 90, p. 200 · A.Everson et al.
  14. Nickel-catalyzed enantioselective Negishi cross-couplings of racemic secondary α-bromo amides with alkylzinc reagents: (S)-N-benzyl-7-cyano-2-ethyl-N-phenylheptanamideCross-coupling Org. Synth. Vol. 87, p. 330 · Lou and Fu
  15. Nickel-catalyzed homoallylation of aldehydes with 1,3-dienes Org. Synth. Vol. 83, p. 88 · Tamarua and Kimurab
  16. Nickel-catalyzed silylolefination of allylic dithioacetals: (E,E)-trimethyl(4-phenyl-1,3-butadienyl)silaneOlefination Org. Synth. Coll. Vol. 9, p. 727; Vol. 70, p. 240 · Ni and Luh
  17. Nickel-catalyzed, geminal dimethylation of allylic dithioacetals: (E)-1-phenyl-3,3-dimethyl-1-butene Org. Synth. Coll. Vol. 9, p. 649; Vol. 74, p. 187 · Yuan and Luh
  18. Nicotinamide-1-oxide Org. Synth. Coll. Vol. 4, p. 704; Vol. 37, p. 63 · Taylor and Crovetti
  19. Nicotinic acid Org. Synth. Coll. Vol. 1, p. 385; Vol. 4, p. 49 · McElvain
  20. Nicotinic anhydride Org. Synth. Coll. Vol. 5, p. 822; Vol. 47, p. 89 · Rinderknecht and Gutenstein
  21. Nicotinonitrile Org. Synth. Coll. Vol. 4, p. 706; Vol. 33, p. 52 · Teague and Short
  22. Nitriles from ketones: cyclohexanecarbonitrile Org. Synth. Coll. Vol. 6, p. 334; Vol. 58, p. 101 · Wender et al.
  23. 4-Nitro-1-naphthylamine Org. Synth. Coll. Vol. 3, p. 664; Vol. 28, p. 80 · Price and Voong
  24. 3'-Nitro-1-phenylethanol by addition of methyltriisopropoxytitanium to m-nitrobenzaldehydeAddition Org. Synth. Coll. Vol. 8, p. 495; Vol. 67, p. 180 · Imwinkelried and Seebach