Olefination 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.
1–6 of 6
- Generation of ynolate and Z-selective olefination of acylsilanes: (Z)-2-methyl-3-trimethylsilyl-2-butenoic acidOlefination
- Nickel-catalyzed silylolefination of allylic dithioacetals: (E,E)-trimethyl(4-phenyl-1,3-butadienyl)silaneOlefination
- Preparation of Horner-Wadsworth-Emmons reagent: methyl 2-benzyloxycarbonylamino-2- (dimethoxy- phosphinyl)acetateOlefination
- Preparation of α,β-unsaturated aldehydes via the Wittig reaction: cyclohexylideneacetaldehydeOlefination
- SYNTHESIS OF (−)-(E,S)-3-(BENZYLOXY)-1-BUTENYL PHENYL SULFONE VIA A HORNER-WADSWORTH-EMMONS REACTION OF (−)-(S)-2-(BENZYLOXY)PROPANAL (Benzene, [[[1-methyl-3-(phenylsulfonyl)-2-propenyl]oxy]methyl]-, [S-(E)]-) from (Propanal, 2-(phenylmethoxy)-, (S)-))Olefination
- Wittig olefination of perfluoroalkyl carboxylic esters; synthesis of 1,1,1-trifluoro-2-ethoxy-5-phenylpent-2-ene and 1-perfluoroalkyl epoxy ethers: 1,1,1-trifluoro-2-ethoxy-2,3-epoxy-5-phenylpentaneOlefination


