1301247-83-5

Upstream product

• 137571-73-4 5,7-dihydroxy-2,2-dimethyl-4H-benzo[d][1,3]dioxin-4-one 
• 83-30-7 acide 2,4,6-trihydroxybenzoique 
• 1301247-95-9 C₂₆H₃₈O₃Si 
• 1301247-78-8 trifluoromethanesulfonic acid 7-methoxymethoxy-2,2-dimethyl-4H-benzo[d][1,3]dioxin-5-yl ester 
• 1301247-77-7 5-hydroxy-7-(methoxymethoxy)-2,2-dimethyl-4H-benzo[d][1,3]dioxin-4-one 
• 1301247-84-6 7-methoxymethoxy-2,2-dimethyl-5-vinyl-4H-benzo[d][1,3]dioxin-4-one 
• 1301247-85-7 1-(6-allyl-3-methoxymethoxy-tetrahydro-pyran-2-yl)-propan-2-ol 
• 1301247-92-6 acetic acid 2-(6-allyl-3-methoxymethoxy-tetrahydro-pyran-2-yl)-1-methyl-ethyl ester 
• 1301247-76-6 1-(tert-butyl-diphenyl-silanyloxy)-6-methyl-hept-5-en-2-ol 
• 1301247-86-8 acetic acid 6-(2-acetoxy-propyl)-5-methoxymethoxy-tetrahydro-pyran-2-yl ester 
• 1301247-99-3 C₁₀H₂₀O₅ 
• 1301247-74-4 5-methoxymethoxy-9-methyl-dec-8-ene-2,4-diol 
• 1301247-90-4 4-hydroxy-5-methoxymethoxy-9-methyl-dec-8-en-2-one 
• 1301247-89-1 C₁₉H₃₈O₄Si 

Relevant academic research and scientific papers

Synthesis of the purported ent -pochonin J structure featuring a stereoselective oxocarbenium allylation

The synthesis of the alleged natural product pochonin J is presented. Key steps of this convergent synthesis include a chemoselective Wacker oxidation, and an Evans anti-reduction of the resulting ketone. Upon ozonolysis, this intermediate undergoes a 6-e