锰
化学
催化作用
选择性
羧酸盐
范围(计算机科学)
组合化学
药物化学
立体化学
有机化学
计算机科学
程序设计语言
作者
Weiping Liu,Sven C. Richter,Yujiao Zhang,Lutz Ackermann
标识
DOI:10.1002/ange.201601560
摘要
Abstract The first manganese(I)‐catalyzed C−H allylations with ample scope were achieved by carboxylate assistance. The highly selective C−H/C−O functionalizations proved viable with densely substituted allyl carbonates, and the organometallic C−H allylation strategy set the stage for expedient late‐stage diversification with excellent levels of positional selectivity.
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