化学
氘
脱质子化
金属化
催化作用
氢
动力学同位素效应
氢-氘交换
光化学
氧化物
药物化学
无机化学
有机化学
量子力学
物理
离子
作者
Junhua Kong,Zhi‐Jiang Jiang,Jiayuan Xu,Yan Li,Hong Cao,Yanan Ding,Bencan Tang,Jia Chen,Zhanghua Gao
标识
DOI:10.1021/acs.joc.1c01411
摘要
A practical and scalable ortho-selective deuteration of aromatic aldehydes was accomplished by Pd-catalyzed hydrogen isotope exchange with deuterium oxide as an inexpensive deuterium source. The use of tert-leucine as a transient directing group facilitates the exchange, affording a wide range of ortho-deuterated aromatic aldehydes with deuterium incorporation up to 97%. The control experiments suggest that the addition of silver trifluoroacetate resists the unexpected reduction of Pd(II), while the theoretical study indicates a rapid reversible concerted metalation–deprotonation process.
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