优化紫外线照射下茶甾醇的合成工艺和光催化机理

IF 1 4区 化学 Q4 CHEMISTRY, MULTIDISCIPLINARY
Wuzhang Liu, Yu Shan, Songtao Liu, Ye Zhou, Yan Wang, Linwei Li, Shu Xu, Yu Chen, Xu Feng, Li Lin, Jinyue Luo, Fei Liu
{"title":"优化紫外线照射下茶甾醇的合成工艺和光催化机理","authors":"Wuzhang Liu, Yu Shan, Songtao Liu, Ye Zhou, Yan Wang, Linwei Li, Shu Xu, Yu Chen, Xu Feng, Li Lin, Jinyue Luo, Fei Liu","doi":"10.1177/17475198241265931","DOIUrl":null,"url":null,"abstract":"Tachysterol is an intermediate product in the synthesis of vitamin D<jats:sub>2</jats:sub> from ergosterol and vitamin D<jats:sub>3</jats:sub> from 7-dehydrocholesterol under ultraviolet irradiation. Recent studies have shown that tachysterol is also a crucial intermediate in the synthesis of the natural anti-tumor product Chaxine C. Although there have been numerous studies on the synthesis of vitamin D<jats:sub>2</jats:sub> and other photoisomers from ergosterol, research on the synthesis of tachysterol is relatively limited. In addition, the yield of tachysterol is not high (57.0%), and the mechanism is unclear. In this study, a method was developed for the qualitative and quantitative analysis of tachysterol. Meanwhile, an efficient synthesis process for tachysterol was reported. The qualitative and quantitative analysis of ergosterol isomers, including tachysterol, a precursor of vitamin D<jats:sub>2</jats:sub>, and photosterol, was conducted using high-performance liquid chromatography, and the quantitative method for tachysterol was confirmed using quantitative nuclear magnetic resonance. There were strong linear relationships between tachysterol content and the testing parameters, with the correlation coefficients of 0.9997 and 0.9971, respectively. The synthesis process of tachysterol from ergosterol through our self-designed photoreactors was optimized, and the effects of reaction temperature, reaction time, photoprotectants, reaction substrate concentration, and the power of ultraviolet lamps were investigated. The yield of the reaction was 85.7%, which is 28.7% higher than the previously reported results. The mechanism and by-products of the reaction were further studied using ultraviolet spectrophotometry and gas chromatography mass spectrometry. This study explored the potential for the large-scale preparation of tachysterol, particularly for the total synthesis of the anti-tumor natural product Chaxine C. It also offered insights into the synthesis of structural similar compounds and the analysis of photocatalytic reaction products.","PeriodicalId":15323,"journal":{"name":"Journal of Chemical Research","volume":"190 1","pages":""},"PeriodicalIF":1.0000,"publicationDate":"2024-08-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Optimization of synthesis process and photocatalytic mechanism of tachysterol under ultraviolet irradiation\",\"authors\":\"Wuzhang Liu, Yu Shan, Songtao Liu, Ye Zhou, Yan Wang, Linwei Li, Shu Xu, Yu Chen, Xu Feng, Li Lin, Jinyue Luo, Fei Liu\",\"doi\":\"10.1177/17475198241265931\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Tachysterol is an intermediate product in the synthesis of vitamin D<jats:sub>2</jats:sub> from ergosterol and vitamin D<jats:sub>3</jats:sub> from 7-dehydrocholesterol under ultraviolet irradiation. Recent studies have shown that tachysterol is also a crucial intermediate in the synthesis of the natural anti-tumor product Chaxine C. Although there have been numerous studies on the synthesis of vitamin D<jats:sub>2</jats:sub> and other photoisomers from ergosterol, research on the synthesis of tachysterol is relatively limited. In addition, the yield of tachysterol is not high (57.0%), and the mechanism is unclear. In this study, a method was developed for the qualitative and quantitative analysis of tachysterol. Meanwhile, an efficient synthesis process for tachysterol was reported. The qualitative and quantitative analysis of ergosterol isomers, including tachysterol, a precursor of vitamin D<jats:sub>2</jats:sub>, and photosterol, was conducted using high-performance liquid chromatography, and the quantitative method for tachysterol was confirmed using quantitative nuclear magnetic resonance. There were strong linear relationships between tachysterol content and the testing parameters, with the correlation coefficients of 0.9997 and 0.9971, respectively. The synthesis process of tachysterol from ergosterol through our self-designed photoreactors was optimized, and the effects of reaction temperature, reaction time, photoprotectants, reaction substrate concentration, and the power of ultraviolet lamps were investigated. The yield of the reaction was 85.7%, which is 28.7% higher than the previously reported results. The mechanism and by-products of the reaction were further studied using ultraviolet spectrophotometry and gas chromatography mass spectrometry. This study explored the potential for the large-scale preparation of tachysterol, particularly for the total synthesis of the anti-tumor natural product Chaxine C. It also offered insights into the synthesis of structural similar compounds and the analysis of photocatalytic reaction products.\",\"PeriodicalId\":15323,\"journal\":{\"name\":\"Journal of Chemical Research\",\"volume\":\"190 1\",\"pages\":\"\"},\"PeriodicalIF\":1.0000,\"publicationDate\":\"2024-08-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Chemical Research\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1177/17475198241265931\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Research","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1177/17475198241265931","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

在紫外线照射下,麦角固醇合成维生素 D2 和 7-脱氢胆固醇合成维生素 D3 的中间产物是水苏糖醇。最近的研究表明,水苏糖醇也是合成天然抗肿瘤产品茶碱 C 的重要中间产物。虽然已有大量研究从麦角甾醇合成维生素 D2 和其他光异构体,但有关水苏糖醇合成的研究却相对有限。此外,塔基甾醇的产率不高(57.0%),机制也不清楚。在本研究中,开发了一种用于定性和定量分析塔基甾醇的方法。同时,报告了一种高效的塔基甾醇合成工艺。利用高效液相色谱法对麦角甾醇异构体(包括维生素 D2 的前体--塔基甾醇和光甾醇)进行了定性和定量分析,并利用定量核磁共振法确认了塔基甾醇的定量方法。塔基醇含量与检测参数之间有很强的线性关系,相关系数分别为 0.9997 和 0.9971。通过自行设计的光反应器对麦角甾醇合成他齐醇的过程进行了优化,考察了反应温度、反应时间、光保护剂、反应底物浓度和紫外灯功率的影响。反应产率为 85.7%,比之前报道的结果高出 28.7%。利用紫外分光光度法和气相色谱质谱法进一步研究了反应的机理和副产物。该研究探索了大规模制备茶甾醇的潜力,特别是抗肿瘤天然产物茶碱 C 的全合成,同时也为合成结构相似的化合物和分析光催化反应产物提供了启示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Optimization of synthesis process and photocatalytic mechanism of tachysterol under ultraviolet irradiation
Tachysterol is an intermediate product in the synthesis of vitamin D2 from ergosterol and vitamin D3 from 7-dehydrocholesterol under ultraviolet irradiation. Recent studies have shown that tachysterol is also a crucial intermediate in the synthesis of the natural anti-tumor product Chaxine C. Although there have been numerous studies on the synthesis of vitamin D2 and other photoisomers from ergosterol, research on the synthesis of tachysterol is relatively limited. In addition, the yield of tachysterol is not high (57.0%), and the mechanism is unclear. In this study, a method was developed for the qualitative and quantitative analysis of tachysterol. Meanwhile, an efficient synthesis process for tachysterol was reported. The qualitative and quantitative analysis of ergosterol isomers, including tachysterol, a precursor of vitamin D2, and photosterol, was conducted using high-performance liquid chromatography, and the quantitative method for tachysterol was confirmed using quantitative nuclear magnetic resonance. There were strong linear relationships between tachysterol content and the testing parameters, with the correlation coefficients of 0.9997 and 0.9971, respectively. The synthesis process of tachysterol from ergosterol through our self-designed photoreactors was optimized, and the effects of reaction temperature, reaction time, photoprotectants, reaction substrate concentration, and the power of ultraviolet lamps were investigated. The yield of the reaction was 85.7%, which is 28.7% higher than the previously reported results. The mechanism and by-products of the reaction were further studied using ultraviolet spectrophotometry and gas chromatography mass spectrometry. This study explored the potential for the large-scale preparation of tachysterol, particularly for the total synthesis of the anti-tumor natural product Chaxine C. It also offered insights into the synthesis of structural similar compounds and the analysis of photocatalytic reaction products.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Chemical Research
Journal of Chemical Research CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
2.30
自引率
0.00%
发文量
66
审稿时长
1.0 months
期刊介绍: The Journal of Chemical Research is a monthly journal which has a broad international authorship and publishes research papers and reviews in all branches of experimental chemistry. Established in 1977 as a joint venture by the British, French and German chemical societies it maintains the high standards set by the founding societies. Each paper is independently peer reviewed and only carefully evaluated contributions are accepted. Recent papers have described new synthetic methods, new heterocyclic compounds, new natural products, and the inorganic chemistry of metal complexes.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信