872676-35-2

Upstream product

• 872676-34-1 5,6-dihydro-2-methyl-4H-furo[2,3-b]pyran-3(2H)-one 
• 5707-04-0 Phenylselenyl chloride 
• 872676-28-3 5,6-dihydro-4H-furo[2,3-b]pyran-3(2H)-one 
• 872676-30-7 3-bromo-2-(prop-2-ynyloxy)tetrahydropyran-2-carboxylic acid methyl ester 

Relevant academic research and scientific papers

The naturally occurring ketene acetal benesudon: Total synthesis and assignment of relative and absolute stereochemistry

(Chemical Equation Presented) The densely functionalized ketene acetal benesudon, which is a bioactive fungal metabolite, was synthesized from D-glucose by a route involving radical cyclization to form the five-membered ring, and oxidative decarboxylation

Synthesis of the core structure of the fungal metabolite benesudon: Use of oxidative decarboxylation

(Chemical Equation Presented) The core structure (5) of the fungal metabolite benesudon (1) was synthesized, the key step being oxidative decarboxylation of acid 17.