Organic Syntheses procedures
3,374 reactions: 10 worked examples with a reagent table you can scale, 503 named reactions and 2,861 checked procedures from Organic Syntheses.
2,737–2,760 of 2,861
- Tributylstannane (Bu3SnH)-catalyzed Barton-McCOMBIE deoxygenation of alcohols: 3-deoxy-1,2:5,6-bis-O-(1-methylethylidene)-α-D-ribo-hexofuranose
- Tricarballylic acid
- Tricarbethoxymethane
- Tricarbomethoxymethane
- Tricarbonyl[(2,3,4,5-η)-2,4-cyclohexadien-1-one]iron and tricarbonyl[(1,2,3,4,5-η)-2-methoxy-2,4-cyclohexadien-1-yl]iron(1+) hexafluorophosphate(1−) from anisole
- 1,1,3-Trichloro-n-nonane
- α,α,α-Trichloroacetanilide
- Trichloroethyl alcohol
- Trichloromethyl chloroformate as a phosgene equivalent: 3-isocyanatopropanoyl chloride
- Trichloromethylphosphonyl dichloride
- p-Tricyanovinyl-N,N-dimethylaniline
- Triethyl carbinol
- Triethyl phosphite
- Triethyloxonium fluoborate
- Trifloroacetyl triflate
- Trifluoroacetylation of amines and amino acids under neutral, mild conditions: N-trifluoroacetanilide and N-trifluoroacetyl-L-tyrosine
- 1,1,1-Trifluoroheptane
- Trifluoromethanesulfonimide-catalyzed (2 + 2)-cycloaddition of silyl enol ethers with α,β-unsaturated esters: 1-(tert-butyldimethylsiloxy)-8-(methoxycarbonyl)-6-methylbicyclo[4.2.0]octaneCycloaddition
- 1-Trifluoromethyl-1-cyclohexanol
- m-Trifluoromethyl-N,N-dimethylaniline
- Trifluoromethylation at the α-position of α,β-unsaturated ketones: 4-phenyl-3-(trifluoromethyl)butan-2-one
- m-Trifluoromethylbenzenesulfonyl chloride
- (3,4,5-Trifluorophenyl)boronic acid-catalyzed amide formation from carboxylic acids and amines: N-benzyl-4-phenylbutyramide
- 5-endo-trig cyclization of 1,1-difluoro-1-alkenes: synthesis of 3-butyl-2-fluoro-1-tosylindoleCyclization
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