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.
505–528 of 3,374
- Woodward cis-hydroxylation The Woodward cis-hydroxylation (also known as the Woodward reaction) is the chemical reaction of alkenes with iodine and silver acetate in wet acetic acid to form cis-diols.(conversion of olefin into cis-diol)
- Wulff–Dötz reaction The Wulff–Dötz reaction (also known as the Dötz reaction or the benzannulation reaction of the Fischer carbene complexes) is the chemical reaction of an aromatic or vinylic alkoxy pentacarbonyl chromium carbene complex with an alkyne and carbon monoxide to give a Cr(CO)3-coordinated substituted phenol.
- Wurtz reaction In organic chemistry, the Wurtz reaction, named after Charles Adolphe Wurtz, is a coupling reaction in which two alkyl halides are treated with sodium metal to form a higher alkane.
- Wurtz–Fittig reaction The Wurtz–Fittig reaction is the chemical reaction of an aryl halide, alkyl halides, and sodium metal to give substituted aromatic compounds.
- Yamaguchi esterification The Yamaguchi esterification is the chemical reaction of an aliphatic carboxylic acid and 2,4,6-trichlorobenzoyl chloride (TCBC, Yamaguchi reagent) to form a mixed anhydride which, upon reaction with an alcohol in the presence of stoichiometric amount of DMAP, produces the desired ester.
- Zincke nitration The Zincke nitration is a nitration reaction in which a bromine is replaced by a nitro group on an electron-rich aryl compound such as a phenol or cresol.
- Zincke reaction The Zincke reaction is an organic reaction, named after Theodor Zincke, in which a pyridine is transformed into a pyridinium salt by reaction with 2,4-dinitro-chlorobenzene and a primary amine.
- Zincke–Suhl reaction The Zincke–Suhl reaction is a special case of a Friedel-Crafts alkylation and was first described by Theodor Zincke and Suhl in 1906.
- Zinin reaction Zinin reaction or Zinin reduction involves reduction of nitro aromatic compounds to the amines using sodium sulfide.
- Abietic acid
- ac-tetrahydro-β-naphthylamine
- Accelerated Suzuki coupling via a ligandless palladium catalyst: 4-methoxy-2'-methylbiphenylCross-coupling
- Acenaphthenequinone
- Acenaphthenol-7
- β-(3-Acenaphthoyl)propionic acid
- Acetal
- Acetamide
- Acetamidine hydrochloride
- 3-Acetamido-2-butanone
- 2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-glucopyranosyl chloride
- p-Acetaminobenzenesulfinic acid
- p-Acetaminobenzenesulfonyl chloride
- α-Acetaminocinnamic acid
- Acetic formic anhydride
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