147169-15-1

Upstream product

• 621-84-1 O-benzyl carbamate 
• 123-72-8 butyraldehyde 
• 824-79-3 sodium 4-methylbenzenesulfinate 

Downstream Products

• 275816-76-7 Z-L-β-homonorvaline 
• 1262848-24-7 1-[1-(p-tosyl)butyl]-2-naphthol 
• 1204133-05-0 C₂₀H₂₆O₅S 
• 646480-70-8 (R/S)-N-benzyloxycarbonylhept-1-en-4-ylamine 
• 271600-11-4 {(S)-1-[2-Oxo-2-((1R,2R,4R)-1,7,7-trimethyl-2-trimethylsilanyloxy-bicyclo[2.2.1]hept-2-yl)-ethyl]-butyl}-carbamic acid benzyl ester 

Relevant academic research and scientific papers

Regioselective arylations of α-amido sulfones with electron-rich arenes through friedel-crafts alkylations catalyzed by ferric chloride hexahydrate: Synthesis of unsymmetrical and bis-symmetrical triarylmethanes

Ferric chloride hexahydrate is a highly efficient catalyst for the regioselective arylation of α-amido sulfones. The products undergo further Friedel-Crafts alkylations with heteroaromatic or electron-rich arenes to afford unsymmetrical or bis-symmetrical

Indium triflate-catalyzed allylation reactions of N-sulfonyl aldimines or N-alkoxycarbonylamino p-tolylsulfones with allyltrimethylsilane: Synthesis of protected homoallylic amines

Indium triflate-catalyzed allylation reactions of N-sulfonyl aldimines or N-alkoxyloxycarbonylamino p-tolylsulfone with allyltrimethylsilane have been successfully developed to produce protected homoallylic amines.

Configurational stability of chiral, nonconjugated nitrogen-substituted organolithium compounds generated by tin-lithium exchange of N-[(1-Tri-n-butylstannyl)alkyl]imidazolidin-2-ones and -oxazolidin-2-ones

Chiral, nonracemic, nonconjugated, acyclic nitrogen-substituted organolithium compounds were generated in order to study the configurational stability of such species. The organolithium compounds were generated by tin-lithium exchange on N-[(1-tri-n-butyl