Synthesis of Spiro[pyrrole–pyrrolizidines] by 1,3-Dipolar Cycloaddition of Azomethine Ylides to 3-Ylidenepyrrol-2-ones
Publication type: Journal Article
Publication date: 2020-07-01
scimago Q4
wos Q4
SJR: 0.190
CiteScore: 1.3
Impact factor: 0.9
ISSN: 10704280, 16083393
Organic Chemistry
Abstract
The Knoevenagel condensation of 1H-pyrrole-2,3-diones with malononitrile gave 3-(dicyanomethylidene)-2,3-dihydro-1H-pyrrole-2-ones which were brought into 1,3-dipolar cycloaddition with azomethine ylides generated in situ from substituted benzaldehydes and proline or sarcosine. The cycloaddition involved the C3=C(CN)2 exocyclic double bond to afford regioisomeric spiro[pyrrole-3,2′-pyrrolizines] and spiro[pyrrole-3,1′-pyrrolizines] or 2,7-diazaspiro[4.4]nonane derivative.
Found
Nothing found, try to update filter.
Found
Nothing found, try to update filter.
Top-30
Journals
|
1
2
|
|
|
Russian Journal of Organic Chemistry
2 publications, 40%
|
|
|
Tetrahedron
1 publication, 20%
|
|
|
Журнал органической химии
1 publication, 20%
|
|
|
ChemistrySelect
1 publication, 20%
|
|
|
1
2
|
Publishers
|
1
2
|
|
|
Pleiades Publishing
2 publications, 40%
|
|
|
Elsevier
1 publication, 20%
|
|
|
Akademizdatcenter Nauka
1 publication, 20%
|
|
|
Wiley
1 publication, 20%
|
|
|
1
2
|
- We do not take into account publications without a DOI.
- Statistics recalculated weekly.
Are you a researcher?
Create a profile to get free access to personal recommendations for colleagues and new articles.
Metrics
5
Total citations:
5
Citations from 2024:
1
(20%)
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Moroz A. A. et al. Synthesis of Spiro[pyrrole–pyrrolizidines] by 1,3-Dipolar Cycloaddition of Azomethine Ylides to 3-Ylidenepyrrol-2-ones // Russian Journal of Organic Chemistry. 2020. Vol. 56. No. 7. pp. 1166-1173.
GOST all authors (up to 50)
Copy
Moroz A. A., Dmitriev M. V., Maslivets A. N. Synthesis of Spiro[pyrrole–pyrrolizidines] by 1,3-Dipolar Cycloaddition of Azomethine Ylides to 3-Ylidenepyrrol-2-ones // Russian Journal of Organic Chemistry. 2020. Vol. 56. No. 7. pp. 1166-1173.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1134/S1070428020070076
UR - https://link.springer.com/10.1134/S1070428020070076
TI - Synthesis of Spiro[pyrrole–pyrrolizidines] by 1,3-Dipolar Cycloaddition of Azomethine Ylides to 3-Ylidenepyrrol-2-ones
T2 - Russian Journal of Organic Chemistry
AU - Moroz, A A
AU - Dmitriev, M V
AU - Maslivets, A N
PY - 2020
DA - 2020/07/01
PB - Pleiades Publishing
SP - 1166-1173
IS - 7
VL - 56
SN - 1070-4280
SN - 1608-3393
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2020_Moroz,
author = {A A Moroz and M V Dmitriev and A N Maslivets},
title = {Synthesis of Spiro[pyrrole–pyrrolizidines] by 1,3-Dipolar Cycloaddition of Azomethine Ylides to 3-Ylidenepyrrol-2-ones},
journal = {Russian Journal of Organic Chemistry},
year = {2020},
volume = {56},
publisher = {Pleiades Publishing},
month = {jul},
url = {https://link.springer.com/10.1134/S1070428020070076},
number = {7},
pages = {1166--1173},
doi = {10.1134/S1070428020070076}
}
Cite this
MLA
Copy
Moroz, A. A., et al. “Synthesis of Spiro[pyrrole–pyrrolizidines] by 1,3-Dipolar Cycloaddition of Azomethine Ylides to 3-Ylidenepyrrol-2-ones.” Russian Journal of Organic Chemistry, vol. 56, no. 7, Jul. 2020, pp. 1166-1173. https://link.springer.com/10.1134/S1070428020070076.
Profiles