New research progress on 56786-63-1 in 2021. Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. In an article, author is NEMOTO, H, once mentioned the application of 56786-63-1, COA of Formula: https://www.ambeed.com/products/56786-63-1.html, Name is (2AR,2’R,4S,5’R,6aR,6bS,8aS,8bR,9S,11aS,12aS,12bS)-2a,4-dihydroxy-5′,6a,8a,9-tetramethylicosahydrospiro[naphtho[2′,1′:4,5]indeno[2,1-b]furan-10,2′-pyran]-2(11aH)-one, molecular formula is C27H42O5, molecular weight is 446.6194, MDL number is MFCD00273330, category is dioxole. Now introduce a scientific discovery about this category.
A novel synthesis of the quaternary substituted chiral cyclobutanone (9) was achieved by the concerted ring expansion of the chiral cyclopropyl epoxide (8) which lead to a formal total synthesis of (-)-frontalin (14).
In the meantime we’ve collected together some recent articles in this area about 56786-63-1 to whet your appetite. Happy reading! COA of Formula: https://www.ambeed.com/products/56786-63-1.html.
Reference:
1,3-Benzodioxole – Wikipedia,
,Dioxole | C3H4O2 – PubChem