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.

2,089–2,112 of 2,861

  1. 1-Phenyl-1-penten-4-yn-3-ol Org. Synth. Coll. Vol. 4, p. 792; Vol. 39, p. 56 · Skattebøl et al.
  2. 3-Phenyl-1-propanol Org. Synth. Coll. Vol. 4, p. 798; Vol. 33, p. 76 · Shriner and Ruby
  3. 4-Phenyl-1,2,4-triazoline-3,5-dione Org. Synth. Coll. Vol. 6, p. 936; Vol. 51, p. 121 · Cookson et al.
  4. trans-1-Phenyl-1,3-butadiene Org. Synth. Coll. Vol. 4, p. 771; Vol. 30, p. 75 · Grummitt and Becker
  5. 1-Phenyl-1,4-pentadiyne and 1-phenyl-1,3-pentadiyne Org. Synth. Coll. Vol. 6, p. 925; Vol. 50, p. 97 · Taniguchi et al.
  6. 2-Phenyl-2-adamantanamine hydrochloride Org. Synth. Coll. Vol. 7, p. 433; Vol. 60, p. 104 · Kalir and Balderman
  7. 1-Phenyl-2-thiobiuret Org. Synth. Coll. Vol. 5, p. 966; Vol. 42, p. 87 · Kurzer and Tertiuk
  8. 2-Phenyl-2-vinylbutyronitrile Org. Synth. Coll. Vol. 6, p. 940; Vol. 55, p. 99 · Makosza et al.
  9. 1-Phenyl-2,3,4,5-tetramethylphosphole Org. Synth. Coll. Vol. 9, p. 653; Vol. 70, p. 272 · Fagan and Nugent
  10. 3-Phenyl-2H-azirine-2-carboxaldehyde Org. Synth. Coll. Vol. 6, p. 893; Vol. 57, p. 83 · Padwa et al.
  11. 1-Phenyl-3-amino-5-pyrazolone Org. Synth. Coll. Vol. 3, p. 708; Vol. 28, p. 87 · Porter and Weissberger
  12. 2-Phenyl-3-n-propylisoxazolidine-4,5-cis-dicarboxylic acid N-phenylimide Org. Synth. Coll. Vol. 5, p. 957; Vol. 46, p. 96 · Brüning et al.
  13. 1-Phenyl-4-phosphorinanone Org. Synth. Coll. Vol. 6, p. 932; Vol. 53, p. 98 · Snider et al.
  14. 2-Phenyl-5-oxazolone Org. Synth. Coll. Vol. 5, p. 946; Vol. 47, p. 101 · VandenBerg et al.
  15. 4-Phenyl-m-dioxane Org. Synth. Coll. Vol. 4, p. 786; Vol. 33, p. 72 · Shriner and Ruby
  16. α-Phenyl-α-carbethoxyglutaronitrile Org. Synth. Coll. Vol. 4, p. 776; Vol. 30, p. 80 · Horning and Finelli
  17. α-Phenyl-β-benzoylpropionitrile Org. Synth. Coll. Vol. 2, p. 498; Vol. 10, p. 80 · Allen and Kimball
  18. Phenyl(trichloromethyl)mercury Org. Synth. Coll. Vol. 5, p. 969; Vol. 46, p. 98 · Logan
  19. (Phenyl)[2-(trimethylsilyl)phenyl]iodonium triflate. An efficient and mild benzyne precursor Org. Synth. Vol. 78, p. 104 · Kitamuraa et al.
  20. Phenylacetamide Org. Synth. Coll. Vol. 4, p. 760; Vol. 32, p. 92 · Wenner
  21. Phenylacetic acid Org. Synth. Coll. Vol. 1, p. 436; Vol. 2, p. 63 · Adams and Thal
  22. α-Phenylacetoacetonitrile Org. Synth. Coll. Vol. 2, p. 487; Vol. 18, p. 66 · Julian et al.
  23. Phenylacetylene Org. Synth. Coll. Vol. 1, p. 438; Vol. 2, p. 67 · Hessler
  24. Phenylacetylene Org. Synth. Coll. Vol. 4, p. 763; Vol. 30, p. 72 · Campbell and Campbell