Song, Changhua published the artcileRegio- and Enantioselective Decarboxylative Allylic Benzylation Enabled by Dual Palladium/Photoredox Catalysis, Related Products of isoquinoline, the main research area is chiral homoallylic alc preparation regioselective enantioselective; allylic acetate phenylacetic acid vinylepoxide decarboxylative benzylation photoredox palladium.
A decarboxylative allylic benzylation cocatalyzed by Pd/photoredox in a regio- and enantioselective manner has been achieved. Readily available aryl acetic acids are used as benzylic nucleophile equivalent without preactivation. This mild and atom economic protocol expands the scope of coupling partners of allylic electrophiles. Vinyl epoxides could also go through this transformation smoothly, affording various chiral homoallylic alcs. bearing all-carbon quaternary stereocenters.
ACS Catalysis published new progress about Alcohols, homoallylic Role: SPN (Synthetic Preparation), PREP (Preparation). 104-01-8 belongs to class isoquinoline, name is 4-Methoxyphenylacetic acid, and the molecular formula is C9H10O3, Related Products of isoquinoline.
Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem