NMR spectroscopic properties of furo[2′,3′:4,5]pyrrolo[1,2-d][1,2,4]triazine derivatives

Authors

  • Ivana Zemanová
  • Renata Gašparová

DOI:

https://doi.org/10.1515/nbec-2017-0020

Keywords:

Chemical shift, furo[3,2-b][pyrrole, NMR spectroscopy

Abstract

The 1H and 13C NMR spectroscopic properties of a series of furo[2′,3′:4,5]pyrrolo[1,2-d][1,2,4]triazin-8(7H)-ones and -thiones were investigated. The influence of various electron donating as well as electron withdrawing substituents at C-5 or N-7 on 1H NMR chemical shifts as well as 13C chemical shifts at C8 were observed. The 5-chloromethyl group had a little influence on the chemical shift of H-7 proton and the 8-thione group causes deshielding of H-7 as well as H-5 protons in comparison with the C-8 carbonyl group.

Downloads

Published

2017-12-29

How to Cite

Zemanová, I. ., & Gašparová, R. . (2017). NMR spectroscopic properties of furo[2′,3′:4,5]pyrrolo[1,2-d][1,2,4]triazine derivatives. Nova Biotechnologica Et Chimica, 16(2), 147–151. https://doi.org/10.1515/nbec-2017-0020

Issue

Vol. 16 No. 2 (2017)

Section

Research Articles

License

All papers published in the Nova Biotechnologica et Chimica (NBC)  are published under a CC-BY licence (CC-BY 4.0). Published materials can be shared (copy and redistribute the material in any medium or format) and adapted (remix, transform, and build upon the material for any purpose, even commercially) with specifying the author(s).