Year: 2026
Type: article
Abstract: High Resolution Image Download MS PowerPoint Slide Controlling regioselectivity in deprotonative arylation of conjugated carbonyl systems remains a longstanding challenge. We report a Pd-catalyzed γ′-arylation of cyclic vinylogous esters (CVEs), enabled by Pd(dba) 2 /cataCXium A and hexamethylphosphoramide (HMPA) as a regioselectivity-governing additive. The method accommodates a broad range of (hetero)aryl bromides and CVE substrates. The resulting γ′-aryl CVEs were further converted to α-arylcycloalkenones via Stork–Danheiser transposition.
Source: Organic Letters
Authors: Yan-Xun Li, Wei-Ting Zhao, Yen-Ku Wu
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $4,500
OpenAlex ID: W7127953664
