IF 4.9 1区 化学 Q1 CHEMISTRY, ORGANIC Organic Letters Pub Date : 2025-02-28 DOI:10.1021/acs.orglett.5c00604
Long Meng, Jia-Yi Pei, Jin-Bao Qiao, Yu-Ming Zhao
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摘要

在之前合成具有代表性的瑞香二萜加拉琼酮的基础上,我们在此报告利用相同的高级中间体化学合成了无水香豆醇,这是瑞香二萜的一种重要降解产物,具有不同的氧化位点。这是通过一系列后期的区域和立体选择性氧化还原操作实现的。这项研究与我们早先合成加拉琼酮的研究相结合,代表了基于单一合成策略合成具有不同氧化位点的瑞诺烷二萜的第一种统一方法。
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Total Synthesis of Anhydroryanodol and Formal Synthesis of Ryanodol and Ryanodine
Building on our prior synthesis of the representative Ryanodane diterpene garajonone, we report here the chemical synthesis of anhydroryanodol, a significant degradation product of Ryanodane diterpenes that features distinct oxidation sites, utilizing the same advanced intermediate. This was accomplished through a series of late-stage regio- and stereoselective redox operations. This study, in conjunction with our earlier synthesis of garajonone, represents the first unified approach to the synthesis of Ryanodane diterpenes with differing oxidation sites based on a single synthetic strategy.
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来源期刊
Organic Letters
Organic Letters 化学-有机化学
CiteScore
9.30
自引率
11.50%
发文量
1607
审稿时长
1.5 months
期刊介绍: Organic Letters invites original reports of fundamental research in all branches of the theory and practice of organic, physical organic, organometallic,medicinal, and bioorganic chemistry. Organic Letters provides rapid disclosure of the key elements of significant studies that are of interest to a large portion of the organic community. In selecting manuscripts for publication, the Editors place emphasis on the originality, quality and wide interest of the work. Authors should provide enough background information to place the new disclosure in context and to justify the rapid publication format. Back-to-back Letters will be considered. Full details should be reserved for an Article, which should appear in due course.
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