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

机译:4,5-二氢-1H-1,2,3-三唑的15 N NMR光谱,互变异构和非对映异构

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Despite the great number of 4,5-dihydro-1H-1,2,3-triazoles synthesized, n15nN NMR data of these heterocycles arenextremely rare. The aim of this paper is to present such data and examples of their application. The compoundsninvestigated have been synthesized according to the given references or procedures. Their n15nN NMR spectra werenmeasured at natural abundance. For some compounds, the chemical shift assignments were confirmed with the helpnof n15nN labelled material. The influences on n15nN chemical shifts of substitution pattern, solvent and concentrationnwere investigated. Additionally, some lanthanide induced shift (LIS) investigations were performed. n13nC labelledncompounds were employed as tools to provide the assignment of tautomeric structures.
机译:尽管合成了大量的4,5-二氢-1H-1,1,2,3-三唑,但这些杂环的n15nN NMR数据极为罕见。本文的目的是介绍此类数据及其应用示例。根据给定的参考文献或程序合成了所研究的化合物。他们的n15nN NMR光谱是在自然丰度下测量的。对于某些化合物,化学位移分配已通过n15nN标记的材料确定。研究了取代模式,溶剂和浓度对n15nN化学位移的影响。此外,还进行了一些镧系元素引起的转变(LIS)研究。 n13nC标记的n化合物被用作提供互变异构结构的工具。

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