volume 39 issue 10 pages 539-547

Synthesis of 1,2,4-oxadiazoles (a review)

Publication typeJournal Article
Publication date2005-10-01
scimago Q4
wos Q4
SJR0.219
CiteScore1.4
Impact factor1.0
ISSN0091150X, 15739031
Drug Discovery
Pharmacology
Abstract
Methods used for the synthesis of 3,5-substituted 1,2,4-oxadiazoles are reviewed. The syntheses are based mostly on the use of primary amidoximes and acylating agents as the initial reactants. The pathway to another large group of 1,2,4-oxadiazoles proceeding from a broad spectrum of reactants is via their reactions of 1,3-dipolar cycloaddition, in particular, with primary amidoximes.
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GOST |
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GOST Copy
Kayukova L. A. Synthesis of 1,2,4-oxadiazoles (a review) // Pharmaceutical Chemistry Journal. 2005. Vol. 39. No. 10. pp. 539-547.
GOST all authors (up to 50) Copy
Kayukova L. A. Synthesis of 1,2,4-oxadiazoles (a review) // Pharmaceutical Chemistry Journal. 2005. Vol. 39. No. 10. pp. 539-547.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1007/s11094-006-0017-7
UR - https://doi.org/10.1007/s11094-006-0017-7
TI - Synthesis of 1,2,4-oxadiazoles (a review)
T2 - Pharmaceutical Chemistry Journal
AU - Kayukova, L A
PY - 2005
DA - 2005/10/01
PB - Springer Nature
SP - 539-547
IS - 10
VL - 39
SN - 0091-150X
SN - 1573-9031
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2005_Kayukova,
author = {L A Kayukova},
title = {Synthesis of 1,2,4-oxadiazoles (a review)},
journal = {Pharmaceutical Chemistry Journal},
year = {2005},
volume = {39},
publisher = {Springer Nature},
month = {oct},
url = {https://doi.org/10.1007/s11094-006-0017-7},
number = {10},
pages = {539--547},
doi = {10.1007/s11094-006-0017-7}
}
MLA
Cite this
MLA Copy
Kayukova, L. A.. “Synthesis of 1,2,4-oxadiazoles (a review).” Pharmaceutical Chemistry Journal, vol. 39, no. 10, Oct. 2005, pp. 539-547. https://doi.org/10.1007/s11094-006-0017-7.