846607-03-2

Upstream product

• 119-61-9 benzophenone 
• 83-30-7 acide 2,4,6-trihydroxybenzoique 
• 57404-76-9 trans-1-heptenylboronic acid 
• 628-71-7 1-Heptyne 
• 846606-83-5 7-benzyloxy-5-(3-pentyl-oxiranyl)-2,2-diphenyl-benzo[1,3]dioxin-4-one 
• 846606-81-3 7-benzyloxy-5-(hept-1-enyl)-2,2-diphenylbenzo[1,3]dioxin-4-one 
• 846606-79-9 trifluoromethanesulfonic acid 7-benzyloxy-4-oxo-2,2-diphenyl-4H-benzo[1,3]dioxin-5-yl ester 
• 846607-02-1 7-(benzyloxy)-5-hydroxy-2,2-diphenyl-4H-benzo[d][1,3]dioxin-4-one 
• 846607-01-0 5,7-dihydroxy-2,2-diphenylbenzo[1,3]dioxin-4-one 
• 846606-85-7 7-benzyloxy-5-(2-oxoheptyl)-2,2-diphenylbenzo[1,3]dioxin-4-one 

Downstream Products

• 846606-99-3 7-methoxy-5-(2-oxoheptyl)-2,2-diphenylbenzo[1,3]dioxin-4-one 

Relevant academic research and scientific papers

A photochemical entry to depsides: Synthesis of gustastatin

(Chemical Equation Presented) Herein, we propose a modular and general strategy to construct orcinol-type depsides based on the photolysis of functionalized benzodioxinones (I). Notably, resorcinylic esters are obtained without competing isocoumarin (II) formation, exemplified by the first total synthesis of gustastatin in 10 steps from commercially available trihydroxybenzoic acid.