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.
2,305–2,328 of 2,861
- Preparation of the COP catalysts: [(S)-COP-OAc]2, [(S)-COP-Cl]2, and (S)-COP-hfacac
- Preparation of thiol esters: S-tert-butyl cyclohexanecarbothioate and S-tert-butyl 3α,7α,12α-trihydroxy-5β-cholane-24-thioate
- Preparation of vinyl trifluoromethanesulfonates: 3-methyl-2-buten-2-yl triflate
- Preparation of α-acetoxy ethers by the reductive acetylation of esters: endo-1-bornyloxyethyl acetate
- Preparation of α-Fluorobis(phenylsulfonyl)methane (FBSM)
- Preparation of α,β-unsaturated aldehydes via the Wittig reaction: cyclohexylideneacetaldehydeOlefination
- Propargylation of alkyl halides: (E)-6,10-dimethyl-5,9-undecadien-1-yne and (E)-7,11-dimethyl-6,10-dodecadien-2-yn-1-ol
- [1.1.1]Propellane
- Propiolaldehyde
- Propionaldehyde
- o-Propiophenol and p-propiophenol
- n-Propyl sulfide
- 2-Propyl-1-azacycloheptane from cyclohexanone oxime
- n-Propylbenzene
- γ-n-Propylbutyrolactone and β-(tetrahydrofuryl)propionic acid
- l-Propylene glycol
- B-Protected haloboronic acids for iterative cross-couplingCross-coupling
- Protection of alcohols using 2-benzyloxy-1-methylpyridinium trifluoromethanesulfonate: methyl (R)-(-)-3-benzyloxy-2-methyl propanoateProtection
- Protection of diols with 4-(tert-butyldimethylsilyloxy)benzylidene acetal and its deprotection: ((4-((4R,5R)-4,5-diphenyl-1,3-dioxolan-2-yl)phenoxy)(tert- butyl)dimethylsilane)Protection
- Protocatechualdehyde
- Protocatechuic acid
- Pseudoionone
- Pseudopelletierine
- Pseudothiohydantoin
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