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.

2,425–2,448 of 2,861

  1. Silver-catalyzed rearrangement of propargylic sulfinates: synthesis of allenic sulfonesRearrangement Org. Synth. Vol. 88, p. 309 · Harmata et al.
  2. Silylation of 2-methyl-2-propen-1-ol dianion: 2-(hydroxymethyl)allyltrimethylsilane Org. Synth. Coll. Vol. 7, p. 266; Vol. 62, p. 58 · Trost et al.
  3. Silylation of ketones with ethyl trimethylsilacetate: (Z)-3-trimethylsiloxy-2-pentene Org. Synth. Coll. Vol. 7, p. 512; Vol. 61, p. 122 · Kuwajima et al.
  4. A simple and convenient method for the oxidation of organoboranes using sodium perborate: (+)-isopinocampheolOxidation Org. Synth. Coll. Vol. 9, p. 522; Vol. 73, p. 116 · Kabalka et al.
  5. A simple and convenient method for the preparation of (Z)-β-iodoacrolein and of (Z)- or (E)-γ-iodo allylic alcohols: (Z)- and (E)-1-iodohept-1-en-3-ol Org. Synth. Coll. Vol. 9, p. 510; Vol. 74, p. 194 · Marek et al.
  6. Simplified Preparation of Dimethyldioxirane (DMDO) Org. Synth. Vol. 90, p. 350 · Taber et al.
  7. Single-step synthesis of alkynyl imines from N-vinyl and N-aryl amides (synthesis of N-[1-phenyl-3-(trimethylsilyl)-2-propynylidene]-benzenamine) Org. Synth. Vol. 85, p. 88 · Movassaghi and Hill
  8. Sodium 2-bromoethanesulfonate Org. Synth. Coll. Vol. 2, p. 558; Vol. 10, p. 96 · Marvel and Sparberg
  9. Sodium amide Org. Synth. Coll. Vol. 3, p. 778; Vol. 20, p. 86 · Bergstrom
  10. Sodium Methoxide-Catalyzed Direct Amidation of Esters Org. Synth. Vol. 91, p. 201 · Agura et al.
  11. Sodium nitromalonaldehyde monohydrate Org. Synth. Coll. Vol. 4, p. 844; Vol. 32, p. 95 · Fanta
  12. Sodium p-arsono-N-phenylglycinamide Org. Synth. Coll. Vol. 1, p. 488; Vol. 8, p. 100 · Jacobs and Heidelberger
  13. Sodium p-hydroxyphenylarsonate Org. Synth. Coll. Vol. 1, p. 490; Vol. 4, p. 65 · Christiansen and Norton
  14. Sodium p-toluenesulfinate Org. Synth. Coll. Vol. 1, p. 492; Vol. 2, p. 89 · Whitmore and Hamilton
  15. Sodium β-styrenesulfonate and β-styrenesulfonyl chloride Org. Synth. Coll. Vol. 4, p. 846; Vol. 34, p. 85 · Rondestvedt and Bordwell
  16. Sorbic acid Org. Synth. Coll. Vol. 3, p. 783; Vol. 24, p. 92 · Allen and VanAllan
  17. Spiro[5.7]trideca-1,4-dien-3-one Org. Synth. Coll. Vol. 7, p. 473; Vol. 61, p. 129 · Kane and Jr
  18. Spiroannelation of enol silanes: 2-oxo-5-METHOXYSPlRO[5.4]decane Org. Synth. Coll. Vol. 9, p. 643; Vol. 72, p. 189 · Lee and Porter
  19. Spiroannelation via organobis(cuprates): 9,9-dimethylspiro[4.5]decan-7-one Org. Synth. Coll. Vol. 9, p. 350; Vol. 70, p. 204 · Wender et al.
  20. (2SR,3RS)-2,4-dimethyl-3-hydroxypentanoic acid Org. Synth. Coll. Vol. 7, p. 185; Vol. 63, p. 89 · Bal et al.
  21. (2SR,3SR)-2,4-dimethyl-3-hydroxypentanoic acid Org. Synth. Coll. Vol. 7, p. 190; Vol. 63, p. 99 · Montgomery et al.
  22. A stable chiral 1,4-dihydropyridine equivalent for the asymmetric synthesis of substituted piperidines: 2-cyano-6-phenyloxazolopiperidine (5H-Oxazolo[3,2-a]pyridine-5-carbonitrile, hexahydro-3-phenyl-, [3R-(3α,5β,8aβ]) Org. Synth. Coll. Vol. 9, p. 176; Vol. 70, p. 54 · Bonin et al.
  23. Stearolic acid Org. Synth. Coll. Vol. 3, p. 785; Vol. 27, p. 76 · Adkins et al.
  24. Stearolic acid Org. Synth. Coll. Vol. 4, p. 851; Vol. 37, p. 77 · Khan et al.