Formal synthesis of (±)-Lycoramine via an acidic Dearomatization–Zn/AcOH reductive elimination sequence

IF 1.5 4区 化学 Q3 CHEMISTRY, ORGANIC Tetrahedron Letters Pub Date : 2025-04-30 Epub Date: 2025-03-25 DOI:10.1016/j.tetlet.2025.155535
Shan-Shan Chen, Xiao-Yang Bi, Bao-Yu Li, Jia-Jun Sui, Zhao-Nan Cai, Hong-Bo Qin
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Abstract

Formal synthesis of (±)-lycoramine was described. The key reaction features a dearomatization-Zn/AcOH promoted reductive elimination sequence, followed by a chemoselective reduction of the double bond in enone yielding compound 1, a key intermediate in the total synthesis of (±)- lycoramine.
2024 Elsevier Ltd. All rights reserved.

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通过酸性脱芳- zn /AcOH还原消除序列正式合成(±)-Lycoramine
描述了(±)-石蒜碱的形式化合成。该关键反应的特点是:zn /AcOH促进了去芳化的还原消除序列,随后是烯酮生成化合物1的双键的化学选择性还原,这是(±)-石蒜碱总合成的关键中间体爱思唯尔有限公司版权所有。
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来源期刊
Tetrahedron Letters
Tetrahedron Letters 化学-有机化学
CiteScore
3.50
自引率
5.60%
发文量
521
审稿时长
28 days
期刊介绍: Tetrahedron Letters provides maximum dissemination of outstanding developments in organic chemistry. The journal is published weekly and covers developments in techniques, structures, methods and conclusions in experimental and theoretical organic chemistry. Rapid publication of timely and significant research results enables researchers from all over the world to transmit quickly their new contributions to large, international audiences.
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