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.

3,241–3,264 of 3,374

  1. 1,3,5-Triacetylbenzene Org. Synth. Coll. Vol. 3, p. 829; Vol. 27, p. 91 · Frank and Varland
  2. 1,3,5-Triacetylbenzene Org. Synth. Vol. 87, p. 192 · Alaimo et al.
  3. 2,4,5-Triaminonitrobenzene Org. Synth. Coll. Vol. 5, p. 1067; Vol. 40, p. 96 · Boyer and Buriks
  4. 1,2,4-Triazole Org. Synth. Coll. Vol. 5, p. 1070; Vol. 40, p. 99 · Ainsworth
  5. Tribiphenylcarbinol Org. Synth. Coll. Vol. 3, p. 831; Vol. 23, p. 95 · Morton et al.
  6. sym.-Tribromobenzene Org. Synth. Coll. Vol. 2, p. 592; Vol. 13, p. 96 · Coleman and Talbot
  7. 2,4,6-Tribromobenzoic acid Org. Synth. Coll. Vol. 4, p. 947; Vol. 36, p. 94 · Robison and Robison
  8. 1,2,3-Tribromopropane Org. Synth. Coll. Vol. 1, p. 521; Vol. 5, p. 99 · Johnson and McEwen
  9. Tributyl(3-methyl-2-butenyl)tin Org. Synth. Coll. Vol. 9, p. 707; Vol. 71, p. 118 · Naruta et al.
  10. Tributylstannane (Bu3SnH)-catalyzed Barton-McCOMBIE deoxygenation of alcohols: 3-deoxy-1,2:5,6-bis-O-(1-methylethylidene)-α-D-ribo-hexofuranose Org. Synth. Vol. 78, p. 239 · Tormo and Fu
  11. Tricarballylic acid Org. Synth. Coll. Vol. 1, p. 523; Vol. 4, p. 77 · Clarke and Murray
  12. Tricarbethoxymethane Org. Synth. Coll. Vol. 2, p. 594; Vol. 17, p. 86 · Lund and Voigt
  13. Tricarbomethoxymethane Org. Synth. Coll. Vol. 2, p. 596; Vol. 13, p. 100 · Corson and Sayre
  14. Tricarbonyl[(2,3,4,5-η)-2,4-cyclohexadien-1-one]iron and tricarbonyl[(1,2,3,4,5-η)-2-methoxy-2,4-cyclohexadien-1-yl]iron(1+) hexafluorophosphate(1−) from anisole Org. Synth. Coll. Vol. 6, p. 996; Vol. 57, p. 107 · Birch and Chamberlain
  15. 1,1,3-Trichloro-n-nonane Org. Synth. Coll. Vol. 5, p. 1076; Vol. 45, p. 104 · Vofsi and Asscher
  16. α,α,α-Trichloroacetanilide Org. Synth. Coll. Vol. 5, p. 1074; Vol. 40, p. 103 · Sukornick
  17. Trichloroethyl alcohol Org. Synth. Coll. Vol. 2, p. 598; Vol. 15, p. 80 · Chalmers
  18. Trichloromethyl chloroformate as a phosgene equivalent: 3-isocyanatopropanoyl chloride Org. Synth. Coll. Vol. 6, p. 715; Vol. 59, p. 195 · Kurita and Iwakura
  19. Trichloromethylphosphonyl dichloride Org. Synth. Coll. Vol. 4, p. 950; Vol. 37, p. 82 · Kennard and Hamilton
  20. p-Tricyanovinyl-N,N-dimethylaniline Org. Synth. Coll. Vol. 4, p. 953; Vol. 39, p. 68 · McKusick and Melby
  21. Triethyl carbinol Org. Synth. Coll. Vol. 2, p. 602; Vol. 11, p. 98 · Moyer and Marvel
  22. Triethyl phosphite Org. Synth. Coll. Vol. 4, p. 955; Vol. 31, p. 111 · Ford-Moore and Perry
  23. Triethyloxonium fluoborate Org. Synth. Coll. Vol. 5, p. 1080; Vol. 46, p. 113 · Meerwein
  24. Trifloroacetyl triflate Org. Synth. Coll. Vol. 7, p. 506; Vol. 64, p. 217 · Taylor et al.