对映选择合成
立体中心
化学
催化作用
组合化学
酮
磷酸
有机化学
作者
Xueting Zhou,Qingqin Huang,Jiami Guo,Lei Dai,Yixin Lü
标识
DOI:10.1002/anie.202310078
摘要
Abstract Chiral α,α‐diaryl ketones are structural motifs commonly present in bioactive molecules, and they are also valuable building blocks in synthetic organic chemistry. However, catalytic asymmetric synthesis of α,α‐diaryl ketones bearing a tertiary stereogenic center remains largely unsolved. Herein, we report a catalytic de novo enantioselective synthesis of α,α‐diaryl ketones from simple alkynes via chiral phosphoric acid (CPA) catalysis. A broad range of enolizable α,α‐diaryl ketones are prepared in good yields and with excellent enantioselectivities. The described protocol also serves as an efficient deuteration method for the preparation of enantiomerically enriched deuterated α,α‐diaryl ketones. Using the methodology reported, bioactive molecules, including one of the best‐selling anti‐breast cancer drugs, tamoxifen, are readily synthesized.
科研通智能强力驱动
Strongly Powered by AbleSci AI