том 11 издание 3 страницы 403-428

Recent Advances in the Synthesis of Heterocycles from Oximes

Edgars Abele
Ramona Abele
Тип публикацииJournal Article
Дата публикации2014-06-25
scimago Q3
wos Q2
БС3
SJR0.377
CiteScore4.0
Impact factor2.5
ISSN15701794, 18756271
Organic Chemistry
Biochemistry
Краткое описание
This review demonstrates that oximes and their derivatives are valuable starting materials for the preparation of many classes of heterocyclic compounds. The main group of reactions includes the cyclization of unsaturated oxime derivatives. Using these starting materials pyrroles, isoxazoles, pyridines and isoquinolines were prepared. Some heterocyclic systems (for example, seven-membered rings) were obtained using the classical Beckmann rearrangement and novel reagents and conditions.
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ГОСТ |
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Abele E., Abele R. Recent Advances in the Synthesis of Heterocycles from Oximes // Current Organic Synthesis. 2014. Vol. 11. No. 3. pp. 403-428.
ГОСТ со всеми авторами (до 50) Скопировать
Abele E., Abele R. Recent Advances in the Synthesis of Heterocycles from Oximes // Current Organic Synthesis. 2014. Vol. 11. No. 3. pp. 403-428.
RIS |
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TY - JOUR
DO - 10.2174/1570179410666131217234916
UR - https://doi.org/10.2174/1570179410666131217234916
TI - Recent Advances in the Synthesis of Heterocycles from Oximes
T2 - Current Organic Synthesis
AU - Abele, Edgars
AU - Abele, Ramona
PY - 2014
DA - 2014/06/25
PB - Bentham Science Publishers Ltd.
SP - 403-428
IS - 3
VL - 11
SN - 1570-1794
SN - 1875-6271
ER -
BibTex |
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@article{2014_Abele,
author = {Edgars Abele and Ramona Abele},
title = {Recent Advances in the Synthesis of Heterocycles from Oximes},
journal = {Current Organic Synthesis},
year = {2014},
volume = {11},
publisher = {Bentham Science Publishers Ltd.},
month = {jun},
url = {https://doi.org/10.2174/1570179410666131217234916},
number = {3},
pages = {403--428},
doi = {10.2174/1570179410666131217234916}
}
MLA
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Abele, Edgars, and Ramona Abele. “Recent Advances in the Synthesis of Heterocycles from Oximes.” Current Organic Synthesis, vol. 11, no. 3, Jun. 2014, pp. 403-428. https://doi.org/10.2174/1570179410666131217234916.