Vitamin D2 from Ergosterol

IF 0.7 Q4 CHEMISTRY, ORGANIC Organic Syntheses Pub Date : 2003-04-28 DOI:10.1002/0471264180.OS076.28
M. Okabe
{"title":"Vitamin D2 from Ergosterol","authors":"M. Okabe","doi":"10.1002/0471264180.OS076.28","DOIUrl":null,"url":null,"abstract":"Vitamin D2 from ergosterol \n \n \n \nintermediate: 3,5-Dinitrobenzoate \n \n \n \n \nreactant: 13.5 g (34 mmol) of ergosterol \n \n \n \n \nintermediate: pre-vitamin 2 \n \n \n \n \nproduct: Vitamin D2 \n \n \n \n \n \nKeywords: \n \nacylation; \ncleavage, miscellaneous; \nelimination, dehydration; \nhydrolysis, esters and lactones; \nphotochemical reactions","PeriodicalId":19576,"journal":{"name":"Organic Syntheses","volume":null,"pages":null},"PeriodicalIF":0.7000,"publicationDate":"2003-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Syntheses","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/0471264180.OS076.28","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 4

Abstract

Vitamin D2 from ergosterol intermediate: 3,5-Dinitrobenzoate reactant: 13.5 g (34 mmol) of ergosterol intermediate: pre-vitamin 2 product: Vitamin D2 Keywords: acylation; cleavage, miscellaneous; elimination, dehydration; hydrolysis, esters and lactones; photochemical reactions
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
麦角甾醇中的维生素D2
关键词:酰化;麦角甾醇中间体;3,5-二硝基苯甲酯反应物;13.5 g (34 mmol)麦角甾醇中间体;乳沟,杂;消除,脱水;水解、酯类和内酯类;光化学反应
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 去求助
来源期刊
Organic Syntheses
Organic Syntheses Chemistry-Organic Chemistry
CiteScore
1.20
自引率
0.00%
发文量
8
期刊介绍: Information not localized
期刊最新文献
Preparation of Radical Clocks Bearing Carbonyl Groups: Synthesis of N-Methoxy-N-methylspiro[cyclopropane-1,9'-fluorene]-2-carboxamide. Preparation of N-Boc-3-methylpyrrole via Anionic Rearrangement Synthesis of Enantioenriched NH-Sulfoximines by NH Transfer to Sulfoxides Using Ammonium Carbamate and (Diacetoxyiodo)benzene Introducing Volume 100 of Organic Syntheses Synthesis of NH-Sulfoximines from Sulfides Using Ammonium Carbamate and (Diacetoxyiodo)benzene to Transfer NH and O
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1