886204-71-3

Upstream product

• 886204-63-3 C₃₈H₃₆O₁₀S₂ 
• 76513-69-4 (2-trimethylethylsilylethoxy)methyl chloride 
• 1001853-66-2 (2S,6S)-2-(4-benzenesulfonyloxyphenyl)-6-[2-(4-benzenesulfonyloxyphenyl)ethyl]tetrahydropyran-4-one 
• 1001853-65-1 4-methoxy-2,6-bis-[2-(trimethylsilyl)ethoxymethoxy]phenylboronic acid 
• 37595-74-7 N,N-phenylbistrifluoromethane-sulfonimide 
• 501-97-3 4-hydroxyphenylpropionic acid 
• 13493-50-0 4-hydroxybenzaldehyde benzenesulfonate ester 
• 98-09-9 benzenesulfonyl chloride 
• 123-08-0 4-hydroxy-benzaldehyde 
• 59434-20-7 1,3,5-tri-O-benzylphloroglucinol 
• 886204-62-2 C₅₈H₅₂O₁₀S₂ 
• 886204-69-9 C₅₁H₄₆O₁₀S₂ 
• 886204-70-2 C₅₂H₄₈O₁₀S₂ 
• 886204-60-0 Acetic acid 3-(4-benzenesulfonyloxy-phenyl)-1-[(S)-1-(4-benzenesulfonyloxy-phenyl)-but-3-enyloxy]-propyl ester 

Downstream Products

• 886204-73-5 C₅₃H₄₆O₁₄S₃ 
• 886204-65-5 C₆₅H₇₄O₁₆S₃Si₂ 
• 252060-62-1 epicalyxin F 
• 886204-72-4 C₅₀H₆₃BrO₁₂S₂Si₂ 

Relevant academic research and scientific papers

Catalytic asymmetric hetero-Diels-Alder route to a key intermediate for the synthesis of calyxin L

A catalytic asymmetric formal synthesis of diarylheptanoid natural product calyxin L has been achieved by incorporating an enantio- and diastereoselective hetero-Diels-Alder (HDA) reaction, a Suzuki-Miyaura coupling, and a stereocontrolled catalytic hydro

Synthesis and structure revision of calyxin natural products

Tandem Prins cyclization and Friedel-Crafts reaction with an electron-rich aromatic ring were used to prepare the core structures of calyxin natural products. The proposed structure of epicalyxin F was prepared and shown to be incorrect. Several calyxin n