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.

2,785–2,808 of 2,861

  1. Trimethylsilyl azide Org. Synth. Coll. Vol. 6, p. 1030; Vol. 50, p. 107 · Birkofer and Wegner
  2. Trimethylsilyl cyanide: cyanosilation of p-benzoquinone Org. Synth. Coll. Vol. 7, p. 517; Vol. 60, p. 126 · Livinghouse
  3. 3-Trimethylsilyl-3-buten-2-one as Michael acceptor for conjugate addition-annelation: cis-4,4a,5,6,7,8-hexahydro-4a,5-dimethyl-2(3H)-naphthalenoneAddition Org. Synth. Coll. Vol. 6, p. 666; Vol. 58, p. 158 · Boeckman et al.
  4. 3-Trimethylsilyl-3-buten-2-one: a Michael acceptorAddition Org. Synth. Coll. Vol. 6, p. 1033; Vol. 58, p. 152 · Boeckman et al.
  5. (Z)-4-(Trimethylsilyl)-3-buten-1-ol Org. Synth. Coll. Vol. 8, p. 609; Vol. 68, p. 182 · Overman et al.
  6. Trimethylsilylacetylene Org. Synth. Coll. Vol. 8, p. 606; Vol. 65, p. 61 · Holmes and Sporikou
  7. Trimethylsilyldiazomethane Org. Synth. Coll. Vol. 8, p. 612; Vol. 68, p. 1 · Shioiri et al.
  8. 2-Trimethylsilylethanesulfonyl chloride (SES-Cl) Org. Synth. Vol. 75, p. 161 · Weinreb et al.
  9. 2-Trimethylsilyloxy-1,3-butadiene as a reactive diene: diethyl trans-4-trimethylsilyloxy-4-cyclohexene-1,2-dicarboxylate Org. Synth. Coll. Vol. 6, p. 445; Vol. 58, p. 163 · Jung and McCombs
  10. Trimyristin Org. Synth. Coll. Vol. 1, p. 538; Vol. 6, p. 100 · Beal
  11. 1,3,5-Trinitrobenzene Org. Synth. Coll. Vol. 1, p. 541; Vol. 2, p. 93 · Clarke and Hartman
  12. 2,4,6-Trinitrobenzoic acid Org. Synth. Coll. Vol. 1, p. 543; Vol. 2, p. 95 · Clarke and Hartman
  13. 2,4,7-Trinitrofluorenone Org. Synth. Coll. Vol. 3, p. 837; Vol. 28, p. 91 · Woolfolk and Orchin
  14. Triphenylaluminum Org. Synth. Coll. Vol. 5, p. 1116; Vol. 45, p. 107 · Neely et al.
  15. Triphenylamine Org. Synth. Coll. Vol. 1, p. 544; Vol. 8, p. 116 · Hager
  16. Triphenylcarbinol Org. Synth. Coll. Vol. 3, p. 839; Vol. 23, p. 98 · Bachmann and Hetzner
  17. Triphenylchloromethane Org. Synth. Coll. Vol. 3, p. 841; Vol. 23, p. 100 · Bachmann
  18. 1,2,3-Triphenylcyclopropenium bromide Org. Synth. Coll. Vol. 9, p. 730; Vol. 74, p. 72 · Xu and Breslow
  19. Triphenylene Org. Synth. Coll. Vol. 5, p. 1120; Vol. 40, p. 105 · Heaney and Millar
  20. Triphenylethylene Org. Synth. Coll. Vol. 2, p. 606; Vol. 17, p. 89 · Adkins and Zartman
  21. 2,3,5-Triphenylisoxazolidine Org. Synth. Coll. Vol. 5, p. 1124; Vol. 46, p. 127 · Brüning et al.
  22. Triphenylmethane Org. Synth. Coll. Vol. 1, p. 548; Vol. 4, p. 81 · Norris
  23. Triphenylmethylsodium Org. Synth. Coll. Vol. 2, p. 607; Vol. 19, p. 83 · Jr and Hauser
  24. 2,4,6-Triphenylnitrobenzene Org. Synth. Coll. Vol. 5, p. 1128; Vol. 49, p. 114 · Dimroth et al.