Bio-based triacetic acid lactone in the synthesis of azaheterocycles via a ring-opening transformation

Research output: Contribution to journalArticleResearchpeer-review

4 Citations (Scopus)
Original languageEnglish
Pages (from-to)8943-8952
Number of pages10
JournalNew Journal of Chemistry
Volume42
Issue number11
DOIs
Publication statusPublished - 1 Jan 2018

Fingerprint

Acids
Amines
Hydrazines
Pyrazoles
Pyridones
Isoxazoles
Dimethylformamide
Hydroxylamine
Organic compounds
Amides
Hydrazine
triacetic acid lactone
1,1-dimethoxyethane
4-pyridone

ASJC Scopus subject areas

  • Catalysis
  • Chemistry(all)
  • Materials Chemistry

WoS ResearchAreas Categories

  • Chemistry, Multidisciplinary

Cite this

@article{3483a1d28abb42ba93957a63069ffb21,
title = "Bio-based triacetic acid lactone in the synthesis of azaheterocycles via a ring-opening transformation",
author = "Obydennov, {Dmitrii L.} and El-Tantawy, {A. I.} and Sosnovskikh, {Vyacheslav Ya}",
year = "2018",
month = "1",
day = "1",
doi = "10.1039/c8nj01044g",
language = "English",
volume = "42",
pages = "8943--8952",
journal = "New Journal of Chemistry",
issn = "1144-0546",
publisher = "Royal Society of Chemistry",
number = "11",

}

Bio-based triacetic acid lactone in the synthesis of azaheterocycles via a ring-opening transformation. / Obydennov, Dmitrii L.; El-Tantawy, A. I.; Sosnovskikh, Vyacheslav Ya.

In: New Journal of Chemistry, Vol. 42, No. 11, 01.01.2018, p. 8943-8952.

Research output: Contribution to journalArticleResearchpeer-review

TY - JOUR

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AU - Obydennov, Dmitrii L.

AU - El-Tantawy, A. I.

AU - Sosnovskikh, Vyacheslav Ya

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SP - 8943

EP - 8952

JO - New Journal of Chemistry

JF - New Journal of Chemistry

SN - 1144-0546

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