1,3-Dipolar cycloaddition reactions of azomethine ylides and alkynes
Тип публикации: Journal Article
Дата публикации: 2018-12-01
scimago Q4
wos Q4
БС3
SJR: 0.243
CiteScore: 2.7
Impact factor: 1.0
ISSN: 00093122, 15738353
Organic Chemistry
Краткое описание
In this review, we consider 1,3-dipolar cycloaddition reactions between azomethine ylides and alkynes, resulting in the formation of pyrroles, as well as their hydrogenated and fused analogs. The references have been arranged according to the types of azomethine ylides and the methods used for their generation. The review is mainly focused on literature sources published since year 2000 and contains 133 references.
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Gulevskaya A. V., Nelina Nemtseva J. I. 1,3-Dipolar cycloaddition reactions of azomethine ylides and alkynes // Chemistry of Heterocyclic Compounds. 2018. Vol. 54. No. 12. pp. 1084-1107.
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Gulevskaya A. V., Nelina Nemtseva J. I. 1,3-Dipolar cycloaddition reactions of azomethine ylides and alkynes // Chemistry of Heterocyclic Compounds. 2018. Vol. 54. No. 12. pp. 1084-1107.
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TY - JOUR
DO - 10.1007/s10593-019-02398-5
UR - https://doi.org/10.1007/s10593-019-02398-5
TI - 1,3-Dipolar cycloaddition reactions of azomethine ylides and alkynes
T2 - Chemistry of Heterocyclic Compounds
AU - Gulevskaya, Anna V
AU - Nelina Nemtseva, Julia I
PY - 2018
DA - 2018/12/01
PB - Springer Nature
SP - 1084-1107
IS - 12
VL - 54
SN - 0009-3122
SN - 1573-8353
ER -
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@article{2018_Gulevskaya,
author = {Anna V Gulevskaya and Julia I Nelina Nemtseva},
title = {1,3-Dipolar cycloaddition reactions of azomethine ylides and alkynes},
journal = {Chemistry of Heterocyclic Compounds},
year = {2018},
volume = {54},
publisher = {Springer Nature},
month = {dec},
url = {https://doi.org/10.1007/s10593-019-02398-5},
number = {12},
pages = {1084--1107},
doi = {10.1007/s10593-019-02398-5}
}
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MLA
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Gulevskaya, Anna V., and Julia I Nelina Nemtseva. “1,3-Dipolar cycloaddition reactions of azomethine ylides and alkynes.” Chemistry of Heterocyclic Compounds, vol. 54, no. 12, Dec. 2018, pp. 1084-1107. https://doi.org/10.1007/s10593-019-02398-5.