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.
2,953–2,976 of 3,374
- Sorbic acid
- Spiro[5.7]trideca-1,4-dien-3-one
- Spiroannelation of enol silanes: 2-oxo-5-METHOXYSPlRO[5.4]decane
- Spiroannelation via organobis(cuprates): 9,9-dimethylspiro[4.5]decan-7-one
- (2SR,3RS)-2,4-dimethyl-3-hydroxypentanoic acid
- (2SR,3SR)-2,4-dimethyl-3-hydroxypentanoic acid
- A stable chiral 1,4-dihydropyridine equivalent for the asymmetric synthesis of substituted piperidines: 2-cyano-6-phenyloxazolopiperidine (5H-Oxazolo[3,2-a]pyridine-5-carbonitrile, hexahydro-3-phenyl-, [3R-(3α,5β,8aβ])
- Stearolic acid
- Stearolic acid
- Stearone
- Stereocontrolled iodolactonization of acyclic olefinic acids: the trans and cis isomers of 4,5-dihydro-5-iodomethyl-4-phenyl-2(3H)-furanone
- Stereocontrolled preparation of 3-acyltetrahydrofurans from acid-promoted rearrangements of allylic ketals: (2S,3S)-3-acetyl-8-carboethoxy-2,3-dimethyl-1-oxa-8-azaspiro[4.5]decaneRearrangement
- Stereoselective 1,4-functionalizations of conjugated dienes: cis- and trans-1-acetoxy-4-(dicarbomethoxymethyl)-2-cyclohexene
- Stereoselective aldol reaction of doubly deprotonated (R)-(+)-2-hydroxy-1,2,2-triphenylethyl acetate (HYTRA): (R)-3-hydroxy-4-methylpentanoic acidCondensation
- Stereoselective alkene synthesis via 1-chloro-1-[(dimethyl)phenylsilyl]alkanes and α-(dimethyl)phenylsilyl ketones: 6-methyl-6-dodecene
- Stereoselective hydroxylation with thallium(I) acetate and iodine: trans- and cis-1,2-cyclohexanediols
- Stereoselective isoprenoid chain extension with acetoacetate dianion: ((E, E, E)-geranylgeraniol from (E, E)-farnesol)
- Stereoselective nickel-catalyzed 1,4-hydroboration of 1,3-dienesAddition
- Stereoselective synthesis of (E)-2,3-dibromobut-2-enoic acid
- Stereoselective synthesis of 2,2-disubstituted 1-fluoro-alkenes: (E)-[[fluoro(2-phenylcyclohexylidene)-methyl]sulfonyl]benzene and (Z)-[2-(fluoromethylene)-cyclohexyl]benzene
- Stereoselective synthesis of 3-arylacrylates by copper-catalyzed syn hydroarylation
- Stereoselective synthesis of anti α-methyl-β-methoxy carboxylic compounds
- Stereoselective synthesis of trisubstituted olefins: ethyl 4-methyl-(E)-4,8-nonadienoate
- Stereospecific reduction of propargyl alcohols: (E)-3-trimethylsilyl-2-propen-1-olReduction
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