Concise Synthesis of (±)-Cephalotaxine

IF 0.8 4区化学 Q4 CHEMISTRY, ORGANIC

Heterocycles Pub Date : 2023-01-01 DOI:10.3987/com-22-14774

Jian Zhang, Hongxia Dai, Huili Ding, Yu Fan, Hui Chen, Ming Jing

引用次数: 0

Abstract

– The construction of 1-azaspiro[4.4]nonane framework was achieved via the key Stevens rearrangement reaction of the Weinreb amide. And the subsequent steps mediated by the carbonyl of Weinreb amide led to the concise formal synthesis of (±)-cephalotaxine. Further development and application of asymmetric Stevens rearrangement of the Weinreb amide are underway. Cephalotaxine

查看原文本刊更多论文

(±)-头孢噻嗪的简明合成

本文章由计算机程序翻译，如有差异，请以英文原文为准。

求助全文

约1分钟内获得全文求助全文

来源期刊

Heterocycles 化学-有机化学

CiteScore

1.50

自引率

0.00%

发文量

108

审稿时长

1 months

期刊介绍： Since its inception in 1973 HETEROCYCLES has provided a platform for the rapid exchange of research in the areas of organic, pharmaceutical, analytical, and medicinal chemistry of heterocyclic compounds in addition to communications, papers, reviews, a special section of the journal presents newly-discovered natural products whose structure has recently been established. Another section is devoted to the total synthesis of previously documented natural products with heterocyclic ring systems. Due to the fact that the journal is able to publish articles within two months of receipt of the manuscripts, researchers in this field can obtain up-to-date information on heterocyclic research by reading Heterocycles regularly. Audience: Organic and Physical Organic Chemists, Biochemists, Pharmacologists and Scientists studying heterocyclic compounds