1361049-69-5

Upstream product

• 521315-88-8 methyl (3R,5R)-3,5-dihydroxy-6-heptenoate 
• 98-88-4 benzoyl chloride 
• 1361049-70-8 methyl (5R)-5-hydroxy-3-oxo-6-heptenoate 
• 1361049-59-3 (+)-lactiflorin 
• 108-24-7 acetic anhydride 
• 1361049-68-4 C₄₄H₄₄O₁₀ 
• 1361049-76-4 C₅₀H₆₀O₁₀Si 
• 1361049-66-2 C₄₃H₅₆O₉Si 
• 1361049-67-3 C₄₇H₆₃ClO₁₁Si 
• 1361049-83-3 C₄₃H₅₈O₁₀Si 
• 1361049-65-1 C₅₃H₆₃ClO₁₂Si 
• 1361049-63-9 (1R,4R,6R,7R,9R)-9-benzoyloxymethyl-7-(tert-butyldimethylsilyloxy)-4-hydroxy-2-oxa-tricyclo[4.2.1.0(4,9)]nonan-3-one 
• 1361049-62-8 (5R,2'R)-3-(benzyloxy)-5-[2'-(tert-butyldimethylsilyloxy)but-3'-enyl]-4-(benzoyloxymethyl)furan-2(5H)-one 
• 1361049-73-1 (5R,2'R)-3-(benzyloxy)-5-[2'-(tert-butyldimethylsilyloxy)but-3'-enyl]-4-(hydroxymethyl)furan-2(5H)-one 

Relevant academic research and scientific papers

Total synthesis of (+)-lactiflorin by an intramolecular [2+2] photocycloaddition

Enlightning synthesis: A light-induced intramolecular [2+2] photocycloaddition reaction (1→2) was the key step in the stereoselective synthesis of (+)-lactiflorin (3) and its triacetate. By comparison with reported analytical data, it was possible to unambiguously elucidate the structure of this natural product, to which three different structures had been previously assigned. Copyright