137475-49-1

Upstream product

• 5707-04-0 Phenylselenyl chloride 
• 110830-54-1 5a-Methyl-3,4,5,5a,6,7-hexahydro-naphtho[1,8-bc]furan-8-one 
• 137475-47-9 3-(4-Methyl-4,5,6,7-tetrahydro-isobenzofuran-4-yl)-propionic acid methyl ester 
• 137475-48-0 3-(4-Methyl-4,5,6,7-tetrahydro-isobenzofuran-4-yl)-propionic acid 
• 129272-05-5 3-(4-Methyl-5-oxo-4,5,6,7-tetrahydro-isobenzofuran-4-yl)-propionic acid methyl ester 
• 129272-04-4 3-(5-Oxo-4,5,6,7-tetrahydro-isobenzofuran-4-yl)-propionic acid methyl ester 
• 129272-01-1 4,5,6,7-tetrahydroisobenzofuran-5-one 

Relevant academic research and scientific papers

Formal total synthesis of xestoquinone via furan ring transfer reaction strategy

A formal total synthesis of the marine natural xestoquinone (5) based upon FRT reaction strategy is accomplished by preparation of the pentacyclic furan 6, an advanced key intermediate in Harada's previous total synthesis of this target.