CAS: 484-12-8; 7-Methoxy-8-(3-Methylbut-2-En-1-yl)-2H-Chromen-2-One

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上下游产品

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在 氢气体系中,用 乙酸乙酯,甲苯 作为反应溶剂,20.0~220.0 °C,101.33 Kpa 条件下,反应 13.0H,反应生成 蛇床子提取物
参考文献:微波辅助合成苯丙烷和香豆素:甾醇的全合成
标题:微波辅助合成苯丙烷和香豆素:甾醇的全合成
摘要:开发了一种微波辅助一锅合成苯丙烷,单木酚和香豆素的方法.选择的反应条件决定了是否反应生成肉桂酸或香豆素衍生物.优化的反应条件也被用于合成薄荷醇(13)和其他几种天然产物.
DOI:10.1002/ejoc.201701021

专利信息

专利号:WO-2025056767-A1
优先权日:2023-09-15
标题 :Process for the preparation of enantiomerically enriched aliphatic amines
发明人：BOU HAMDAN FARHAN; GODINEAU EDOUARD; SMEJKAL TOMAS; DUMEUNIER RAPHAEL; BOUSSEMGHOUNE MOHAMED ABDELOUAHAB; BLUM MATHIAS
权利人:SYNGENTA CROP PROTECTION AG
摘要:The present invention relates to a process for the preparation of enantiomerically enriched cyclobutylamines of formula (I) from α-tertiary cyclobutanones and reacting said enantiomerically enriched cyclobutylamines to enantiomerically enriched cyclobutylamides. Such compounds are useful intermediates in the synthesis of microbiocidal thiazole compounds.

专利号:CN-101456853-A
优先权日:2009-01-05
标题:Synthesis of a new series of biomimetic compounds 7-alkoxy-8-(3,3'-disubstituted propyl)benzopyran-2-ones and their application as pesticides

专利号:CN-101456852-A
优先权日:2008-12-22
标 题:A new method for the synthesis of osthole derivatives

专利号:WO-2021038306-A1
优先权日:2019-08-28
标 题 :Selenophenochromene phosphonic acids, preparation and use as antiproliferative agents
发明人：ARSENJANS PAVELS; DOMRACEVA ILONA; PAEGLE EDGARS
权利人:LATVIAN INST ORGANIC SYNTHESIS
摘要:The present invention relates to a novel selenophenochromene phosphonic acids as antiproliferative agents, as well as methods of their manufacturing and use in different pharmaceutical compositions for the treatment or prevention of various diseases and disorders by administration of such substances.

专利号:CN-116832060-A
优先权日:2023-08-18
标题 :A kind of Cnidium monnieri extract-mediated synthesis of nano-silver material and its preparation method and application

专利号:US-11285169-B2
优先权日:2013-03-13
标题 :Methods for modulating chemotherapeutic cytotoxicity
发明人：ROBERTS DAVID D; SOTO PANTOJA DAVID R
权利人:US HEALTH
摘要:Methods of reducing cytotoxicity of a chemotherapeutic agent to non-cancer cells by administering to a subject with cancer an effective amount of an agent that inhibits CD47 signaling and a DNA damaging agent, such as an anthracycline, topoisomerase inhibitor, or nucleotide synthesis inhibitor, are provided. Example disclosed methods reduce cardiotoxicity. In one example, the methods include administering to a subject with cancer an effective amount of a CD47 antisense morpholino oligonucleotide and an anthracycline such as doxorubicin. Methods of increasing cytotoxicity of a chemotherapeutic agent in cancer cells by administering to a subject with a tumor an effective amount of an agent that inhibits CD47 signaling and a DNA damaging agent such as an anthracycline, topoisomerase inhibitor, or nucleotide synthesis inhibitor, are also provided. In some embodiments, the inhibitor of CD47 signaling is administered to the subject before, during, or after the administration of the DNA damaging agent.