167764-30-9

Upstream product

• 7669-54-7 2-nitrobenzenesulfenyl chloride 
• 167764-29-6 [5-(2-tert-butylsulfanyl-propionyl)-2-methoxy-phenyl]-acetic acid 
• 107-47-1 sulfure de di tert-butyle 
• 29364-29-2 sodium tert-butyl thiolate 
• 68-12-2 N,N-dimethyl-formamide 
• 167764-27-4 methyl [3-(2-bromopropionyl)-6-methoxyphenyl]acetate 
• 167764-28-5 3-(2-chloropropionyl)-6-methoxyphenylacetic acid 
• 27798-60-3 methyl 2-(2-methoxyphenyl)acetate 
• 93-25-4 2-methoxyphenylacetic acid 

Downstream Products

• 644-08-6 4-Methylbiphenyl 
• 3218-36-8 4-Phenylbenzaldehyde 

Relevant academic research and scientific papers

Solid-phase synthesis utilizing photochemical carbon-sulfur bond cleavage of thioethers

A method for photochemical cleavage of carbon-sulfur bonds in conjunction with solid-phase synthesis utilizing a deoxygenated solvent and light to cleave the carbon-sulfur bond from a heterogeneous support. Also disclosed are compounds for use with said p

Solid-Phase Synthetic Methods in Combinatorial Chemistry

The gel-phase carbon NMR spectra of various polymer supports are evaluated as to their suitability in the production of non-peptide combinatorial libraries. The solid-phase synthesis of biphenyls as scaffolds for the production of combinatorial libraries is also described. Both substituted and unsubstituted trialkylphenyltins were shown to undergo heterogenous palladium-catalyzed Stille coupling with aryl electrophiles to give after photolytic cleavage using the NpSSMpact linker biphenyls containing no residual amide, carboxylic acid, or alcohol appendages.