Pyrrole ring opening – pyridine ring closure: Recyclization of 2-(2-oxo-1,2-dihydro-3H-pyrrol-3-ylidene)malononitriles into highly functionalized nicotinonitriles
Publication type: Journal Article
Publication date: 2020-01-01
scimago Q3
wos Q3
SJR: 0.334
CiteScore: 3.2
Impact factor: 1.5
ISSN: 00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
A series of novel N,N-dialkyl-2-amino-3-cyanoisonicotinamides were synthesized in good to high yields (61–84%) via the reaction of 2-(5-aryl-2-oxo-1H-pyrrol-3(2H)-ylidene)malononitriles and amines according to the ANRORC process. The developed approach represents a novel method for the synthesis of functionalized nicotinonitriles.
Found
Nothing found, try to update filter.
Found
Nothing found, try to update filter.
Top-30
Journals
|
1
|
|
|
New Journal of Chemistry
1 publication, 25%
|
|
|
Synthetic Communications
1 publication, 25%
|
|
|
Chemistry of Heterocyclic Compounds
1 publication, 25%
|
|
|
Environmental Science and Pollution Research
1 publication, 25%
|
|
|
1
|
Publishers
|
1
2
|
|
|
Springer Nature
2 publications, 50%
|
|
|
Royal Society of Chemistry (RSC)
1 publication, 25%
|
|
|
Taylor & Francis
1 publication, 25%
|
|
|
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
4
Total citations:
4
Citations from 2024:
0
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Milovidova A. G. et al. Pyrrole ring opening – pyridine ring closure: Recyclization of 2-(2-oxo-1,2-dihydro-3H-pyrrol-3-ylidene)malononitriles into highly functionalized nicotinonitriles // Tetrahedron Letters. 2020. Vol. 61. No. 2. p. 151368.
GOST all authors (up to 50)
Copy
Milovidova A. G., Tafeenko V. A., Nasakin O. E., Belikov M. Yu., Ievlev M. Y., Ершов О. Pyrrole ring opening – pyridine ring closure: Recyclization of 2-(2-oxo-1,2-dihydro-3H-pyrrol-3-ylidene)malononitriles into highly functionalized nicotinonitriles // Tetrahedron Letters. 2020. Vol. 61. No. 2. p. 151368.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1016/j.tetlet.2019.151368
UR - https://doi.org/10.1016/j.tetlet.2019.151368
TI - Pyrrole ring opening – pyridine ring closure: Recyclization of 2-(2-oxo-1,2-dihydro-3H-pyrrol-3-ylidene)malononitriles into highly functionalized nicotinonitriles
T2 - Tetrahedron Letters
AU - Milovidova, Angelina G
AU - Tafeenko, Viktor A.
AU - Nasakin, Oleg E
AU - Belikov, Mikhail Yu
AU - Ievlev, Mikhail Yu.
AU - Ершов, О.В.
PY - 2020
DA - 2020/01/01
PB - Elsevier
SP - 151368
IS - 2
VL - 61
SN - 0040-4039
SN - 1873-3581
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2020_Milovidova,
author = {Angelina G Milovidova and Viktor A. Tafeenko and Oleg E Nasakin and Mikhail Yu Belikov and Mikhail Yu. Ievlev and О.В. Ершов},
title = {Pyrrole ring opening – pyridine ring closure: Recyclization of 2-(2-oxo-1,2-dihydro-3H-pyrrol-3-ylidene)malononitriles into highly functionalized nicotinonitriles},
journal = {Tetrahedron Letters},
year = {2020},
volume = {61},
publisher = {Elsevier},
month = {jan},
url = {https://doi.org/10.1016/j.tetlet.2019.151368},
number = {2},
pages = {151368},
doi = {10.1016/j.tetlet.2019.151368}
}
Cite this
MLA
Copy
Milovidova, Angelina G., et al. “Pyrrole ring opening – pyridine ring closure: Recyclization of 2-(2-oxo-1,2-dihydro-3H-pyrrol-3-ylidene)malononitriles into highly functionalized nicotinonitriles.” Tetrahedron Letters, vol. 61, no. 2, Jan. 2020, p. 151368. https://doi.org/10.1016/j.tetlet.2019.151368.
Profiles