Abstract
An efficient new synthesis of 5,7-dihydroxy-4-methylisobenzofuran-l(3H)-one, a metabolite of aspergillus flavus and a key intermediate in the synthesis of mycophenolic acid, is reported. The new synthesis involves the preparation of l,2-dihydro-4,6-dimethoxy-3-methylbenzo-cyclobuten-l-ol and a regioselective β-scission of alkoxyl radical generated from it with lead tetraacetate as the key steps.
Cite
CITATION STYLE
Kobayashi, K., Shimizu, H., Itoh, M., & Suginome, H. (1990). An efficient synthesis of 5,7-dihydroxy-4-methylisobenzofuran-l(3H)-one, a metabolite of aspergillus flavus and a key intermediate in the synthesis of mycophenolic acid. Bulletin of the Chemical Society of Japan, 63(8), 2435–2437. https://doi.org/10.1246/bcsj.63.2435
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.