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.
2,785–2,808 of 3,374
- Preparation of cyano compounds using alkylaluminum intermediates: 1-cyano-6-methoxy-3,4-dihydronaphthalene
- Preparation of cyanoalkynes: 3-phenyl-2-propynenitrile
- Preparation of Cyclobutenone
- Preparation of cycloheptane-1,3-dione via reductive ring expansion of 1-trimethylsilyloxy-7,7-dichlorobicyclo[3.2.0]heptan-6-one
- Preparation of DABSO from Karl-Fischer reagent
- Preparation of Enantioenriched Homoallylic Primary Amines
- Preparation of enantiomerically enriched (1S)-1-phenylpropan-1-amine hydrochloride by a catalytic addition of diorganozinc reagents to iminesAddition
- Preparation of enantiomerically pure (R,R)-BozPHOS
- Preparation of enantiomerically pure α-N,N-dibenzylamino aldehydes: S-2-(N,N-dibenzylamino)-3-phenylpropanal
- Preparation of ethyl 1-benzyl-4-fluoropiperidine-4-carboxylate
- Preparation of H,4 PyrrolidineQuin-BAM (PBAM)
- Preparation of hexakis(4-bromophenyl)benzene (HBB)
- Preparation of Horner-Wadsworth-Emmons reagent: methyl 2-benzyloxycarbonylamino-2- (dimethoxy- phosphinyl)acetateOlefination
- Preparation of hydrazones: acetophenone hydrazone
- Preparation of isopropyl 2-diazoacetyl(phenyl)carbamate
- Preparation of low-halide methyllithium
- Preparation of N-aminoaziridines: trans-1-amino-2,3-diphenylaziridine, 1-amino-2-phenylaziridine, and 1-amino-2-phenylaziridinium acetate
- Preparation of N-aryl-5R-hydroxymethyl-2-oxazolidinones from N-aryl carbamates: N-phenyl-(5R)-hydroxymethyl- 2-oxazolidinone
- Preparation of n-butyl 4-chlorophenyl sulfide
- Preparation of n-Isopropylidene-n'-2-Nitrobenzenesulfonyl Hydrazine (IPNBSH) and Its Use in Palladium-catalyzed Synthesis of Monoalkyl Diazenes. Synthesis of 9-Allylanthracene
- Preparation of N-p-tolylsulfonyl-(E)-1-phenylethylideneimine
- Preparation of N1-Phenylacetamidine 4-Bromobenzoate Using 2,2,2-Trichloroethyl Acetimidate Hydrochloride
- Preparation of O-allyl-N-(9-anthracenylmethyl)cinchonidinium bromide as a phase transfer catalyst for the enantioselective alkylation of glycine benzophenone imine tert-butyl ester: (4S)-2-(benzhydrylidenamino)pentanedioic acid, 1-tert-butyl ester-5-methyl ester
- Preparation of O-esters from the corresponding thiol esters: tert-butyl cyclohexanecarboxylate
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