797789-08-3

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 252286-43-4 {4-[(3,5-dimethyl-benzylamino)-methyl]-phenyl}-methanol 

Downstream Products

• 864249-78-5 (4-chloromethyl-benzyl)-(3,5-dimethyl-benzyl)-carbamic acid tert-butyl ester 
• 1392438-89-9 C₂HCl₃O₂*C₂₆H₂₉NO₂ 
• 1392438-93-5 C₃₁H₃₇NO₄ 
• 1360559-00-7 C₄₂H₅₃NO₄Si 
• 864249-79-6 (3,5-dimethyl-benzyl)-(4-iodomethyl-benzyl)-carbamic acid tert-butyl ester 
• 797789-10-7 3,4-bis-bromomethyl-benzoic acid 4-{[tert-butoxycarbonyl-(3,5-dimethyl-benzyl)-amino]-methyl}-benzyl ester 

Relevant academic research and scientific papers

End-cap exchange of rotaxane by the Tsuji-Trost allylation reaction

(Chemical Equation Presented) Rotaxanes possessing a cinnamyl ester group at the axle terminal were prepared. The terminal end-cap was modified with a bulky malonate ester in excellent yield by the Tsuji-Trost allylation reaction, which was carried out in the presence of a palladium catalyst.

End-capping of a pseudorotaxane via diels-alder reaction for the construction of C60-terminated [2]rotaxanes

(Chemical Equation Presented) The Diels-Alder reaction of various dienophiles such as C60 with a pseudorotaxane having a sultine moiety afforded corresponding [2]-rotaxanes in moderate yields. The introduction of a porphyrin moiety on the wheel