化学
筑地反应
图书馆学
高分子科学
烯丙基重排
有机化学
催化作用
计算机科学
作者
Nathan B. Bennett,Douglas C. Duquette,Jimin Kim,Wen‐Bo Liu,Alexander N. Marziale,Douglas C. Behenna,Scott C. Virgil,Brian M. Stoltz
标识
DOI:10.1002/chem.201300030
摘要
Lactams and imides have been shown to consistently provide enantioselectivities substantially higher than other substrate classes previously investigated in the palladium-catalyzed asymmetric decarboxylative allylic alkylation.We have designed several new substrates to probe the contributions of electronic, steric, and stereoelectronic factors that distinguish the lactam/imide series as superior alkylation substrates.These studies culminated in marked improvements on carbocyclic allylic alkylation substrates.
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