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.
601–624 of 3,374
- 1-d-Aldehydes from organometallic reagents: 2-methylbutanal-1-d
- Aldehydes from primary alcohols by oxidation with chromium trioxide: heptanalOxidation
- Aldehydes from sym-trithiane: n-pentadecanal
- Aliphatic and aromatic β-keto esters from monoethyl malonate: ethyl 2-butyrylacetate
- Alkenes via Hofmann elimination: use of ion-exchange resin for preparation of quaternary ammonium hydroxides: diphenylmethyl vinyl etherRearrangement
- 2-Alkenyl carbinols from 2-halo ketones: 2-E-propenylcyclohexanol
- Alkoxycarbonylation of propargyl chloride: methyl 4-chloro-2-butynoate
- Alkyl and alkylene bromides (I. Hydrobromic acid method)
- Alkyl iodides: neopentyl iodide and iodocyclohexane
- 3-Alkyl-1-alkynes synthesis: 3-ethyl-1-hexyne
- β-Alkyl-α,β-unsaturated esters from enol phosphates of β-keto esters: methyl 2-methyl-1-cyclohexene-1-carboxylate
- 3-Alkylated and 3-acylated indoles from a common precursor: 3-benzylindole and 3-benzoylindole
- Alkylation of dimedone with a tricarbonyl(diene)iron complex: tricarbonyl[2-[(2,3,4,5-η)-4-methoxy-2,4-cyclohexadien-1-yl]-5,5-dimethyl-1,3-cyclohexanedione]iron
- Alkylation of isoquinolines via 2-benzoyl-1,2-dihydroisoquinaldonitriles: 1-benzylisoquinoline
- α-tert-Alkylation of ketones: 2-tert-pentylcyclopentanone
- Alkylation of the anion from Birch reduction of o-anisic acid: 2-heptyl-2-cyclohexenoneReduction
- Alkylations of aldehydes via reaction of the magnesioenamine salt of an aldehyde: 2,2-dimethyl-3-phenylpropionaldehyde
- Alkylations using hexacarbonyl(propargylium)dicobalt salts: 2-(1-methyl-2-propynyl)cyclohexanone
- Alkylidenation of ester carbonyl groups: (Z)-1-ethoxy-1-phenyl-1-hexene
- N-Alkylindoles from the alkylation of sodium indolide in hexamethylphosphoric triamide: 1-benzylindole
- (R)-Alkyloxiranes of high enantiomeric purity from (S)-2-chloroalkanoic acids via (S)-2-chloro-1-alkanols: (R)-methyloxirane
- Alkyne via solid-liquid phase-transfer catalyzed dehydrohalogenation: acetylene dicarboxaldehyde tetramethyl acetal and acetylene dicarboxaldehyde dimethyl acetalHalogenation
- Alkynes via phase transfer–catalyzed dehydrohalogenation: propiolaldehyde diethyl acetalHalogenation
- Alkynyl(phenyl)iodonium tosylates: preparation and stereospecific coupling with vinylcopper reagents. Formation of conjugated enynes. 1-Hexynyl(phenyl)iodonium tosylate and (E)-5-phenyldodec-5-en-7-yneCross-coupling
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