15N NMR spectra, tautomerism and diastereomerism of 4,5-dihydro-1H-1,2,3-triazoles

K. Banert, Jens Lehmann, H. Quast, G. Meichsner, D. Regnat, B. Seiferling
{"title":"15N NMR spectra, tautomerism and diastereomerism of 4,5-dihydro-1H-1,2,3-triazoles","authors":"K. Banert, Jens Lehmann, H. Quast, G. Meichsner, D. Regnat, B. Seiferling","doi":"10.1039/B107326E","DOIUrl":null,"url":null,"abstract":"Despite the great number of 4,5-dihydro-1H-1,2,3-triazoles synthesized, 15N NMR data of these heterocycles are extremely rare. The aim of this paper is to present such data and examples of their application. The compounds investigated have been synthesized according to the given references or procedures. Their 15N NMR spectra were measured at natural abundance. For some compounds, the chemical shift assignments were confirmed with the help of 15N labelled material. The influences on 15N chemical shifts of substitution pattern, solvent and concentration were investigated. Additionally, some lanthanide induced shift (LIS) investigations were performed. 13C labelled compounds were employed as tools to provide the assignment of tautomeric structures.","PeriodicalId":17267,"journal":{"name":"Journal of The Chemical Society-perkin Transactions 1","volume":"68 1","pages":"126-134"},"PeriodicalIF":0.0000,"publicationDate":"2002-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The Chemical Society-perkin Transactions 1","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/B107326E","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Despite the great number of 4,5-dihydro-1H-1,2,3-triazoles synthesized, 15N NMR data of these heterocycles are extremely rare. The aim of this paper is to present such data and examples of their application. The compounds investigated have been synthesized according to the given references or procedures. Their 15N NMR spectra were measured at natural abundance. For some compounds, the chemical shift assignments were confirmed with the help of 15N labelled material. The influences on 15N chemical shifts of substitution pattern, solvent and concentration were investigated. Additionally, some lanthanide induced shift (LIS) investigations were performed. 13C labelled compounds were employed as tools to provide the assignment of tautomeric structures.
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
1,2,3- 4,5-二氢- 1h -1,2,3-三唑的15N核磁共振波谱、互变异构和非对映异构
尽管合成了大量的4,5-二氢- 1h -1,2,3-三唑,但这些杂环的15N NMR数据却极为罕见。本文的目的是介绍这些数据及其应用实例。所研究的化合物是根据给定的参考文献或程序合成的。它们的15N核磁共振谱以自然丰度测量。对于一些化合物,化学位移赋值在15N标记材料的帮助下得到了确认。考察了取代模式、溶剂和浓度对15N化学位移的影响。此外,还进行了一些镧系元素诱导位移(LIS)的研究。13C标记的化合物被用作工具来提供互变异构结构的分配。
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
自引率
0.00%
发文量
0
期刊最新文献
Diaryldiacyloxyspirosulfuranes. Part 4. A kinetic study on the mechanism of hydrolysis The synthesis of some water insoluble dyes for the measurement of pH in water immiscible solvents A new oxindole synthesis Oxidation chemistry of adenine and hydroxyadenines at pyrolytic graphite electrodes Hydrolysis and alkylating reactivity of aromatic nitrogen mustards
×
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