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.
1,297–1,320 of 3,374
- Diallylamine
- Diallylcyanamide
- Diamantane: pentacyclo[7.3.1.14,12.02,7.06,11]tetradecane
- 2,5-Diamino-3,4-dicyanothiophene
- 1,2-Diamino-4-nitrobenzene
- 2,4-Diamino-6-hydroxypyrimidine
- 4,4'-Diaminoazobenzene
- 4,4'-Diaminodiphenylsulfone
- Diaminomaleonitrile (hydrogen cyanide tetramer)
- 2,3-Diaminopyridine
- 2,4-Diaminotoluene
- Diaminouracil hydrochloride
- 1,2-Diaroylcyclopropanes: trans-1,2-dibenzoylcyclopropane
- Diastereoselective aldol condensation using a chiral oxazolidinone auxiliary: (2S*,3S*)-3-hydroxy-3-phenyl-2-methylpropanoic acidCondensation
- Diastereoselective formation of trans-1,2-disubstituted cyclohexanes from alkylidenemalonates by an intramolecular ene reaction: dimethyl (1'R,2'R,5'R)-2-(2'-isopropenyl-5'-methylcyclohex-1'-yl)-propane-1,3-dioate
- Diastereoselective homologation of D-(R)-glyceraldehyde acetonide using 2-(trimethylsilyl)thiazole: 2-O-benzyl-3,4-isopropylidene-D-erythrose
- Diastereoselective synthesis of protected vicinal amino alcohols: (S)-2-[(4S)-N-tert-butoxycarbonyl-2,2-dimethyl-1,3-oxazolidinyl]-2-tert-butyldimethylsiloxyethanal from a serine-derived aldehyde
- Diastereoselective α-alkylation of β-hydroxycarboxylic esters through alkoxide enolates: diethyl (2S, 3R)-(+)-3-allyl-2-hydroxysuccinate from diethyl (S)-(−)-malate
- Diasteroselective formation of α-methoxycarbonyl lactones through an intramolecular Diels–Alder reaction: (4RS,4aRS,6RS,8aRS)-, (4S,4aS,6S,8aS)- and (4R,4aR,6R,8aR)-4-methoxycarbonyl-1,1,6-trimethyl-1,4,4a,5,6,7,8,8a-octahydro-2,3-benzopyrone [rac-5, (+)-5, and (−)-5]
- 4,13-Diaza-18-crown-6
- Diazo ketone cyclization onto a benzene ring: 3,4-dihydro-1(2H)-azulenoneCyclization
- Diazo transfer by means of phase-transfer catalysis: di-tert-butyl diazomalonate
- Diazoacetophenone
- Diazoaminobenzene
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