volume 50 issue 7 pages 1017-1021

Five-membered 2,3-dioxo heterocycles: CV. Reaction of methyl 1-aryl-3-aroyl-4,5-dioxo-4,5-dihydro-1H-pyrrole-2-carboxylates with methyl 2-arylamino-4-(2-naphthyl)-4-oxobut-2-enoates. Crystal and molecular structure of substituted 1,7-diazaspiro[4.4]nonane

Publication typeJournal Article
Publication date2014-07-01
scimago Q4
wos Q4
SJR0.190
CiteScore1.3
Impact factor0.9
ISSN10704280, 16083393
Organic Chemistry
Abstract
Methyl 1-aryl-3-aroyl-4,5-dioxo-4,5-dihydro-1H-pyrrole-2-carboxylates reacted with methyl 2-arylamino-4-(2-naphthyl)-4-oxobut-2-enoates to give methyl 1,7-diaryl-4-aroyl-3-hydroxy-9-(2-naphthalen-2-ylcarbonyl)-2,6-dioxo-1,7-diazaspiro[4.4]nona-3,8-diene-8-carboxylates.
Found 
Found 

Top-30

Journals

1
2
3
Russian Journal of Organic Chemistry
3 publications, 42.86%
Mini-Reviews in Organic Chemistry
1 publication, 14.29%
Chemistry of Heterocyclic Compounds
1 publication, 14.29%
RSC Advances
1 publication, 14.29%
European Journal of Organic Chemistry
1 publication, 14.29%
1
2
3

Publishers

1
2
3
Pleiades Publishing
3 publications, 42.86%
Bentham Science Publishers Ltd.
1 publication, 14.29%
Springer Nature
1 publication, 14.29%
Royal Society of Chemistry (RSC)
1 publication, 14.29%
Wiley
1 publication, 14.29%
1
2
3
  • 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
7
Share
Cite this
GOST |
Cite this
GOST Copy
Denislamova E. S. et al. Five-membered 2,3-dioxo heterocycles: CV. Reaction of methyl 1-aryl-3-aroyl-4,5-dioxo-4,5-dihydro-1H-pyrrole-2-carboxylates with methyl 2-arylamino-4-(2-naphthyl)-4-oxobut-2-enoates. Crystal and molecular structure of substituted 1,7-diazaspiro[4.4]nonane // Russian Journal of Organic Chemistry. 2014. Vol. 50. No. 7. pp. 1017-1021.
GOST all authors (up to 50) Copy
Denislamova E. S., Dubovtsev A. Yu., Slepukhin P. A., Maslivets A. N. Five-membered 2,3-dioxo heterocycles: CV. Reaction of methyl 1-aryl-3-aroyl-4,5-dioxo-4,5-dihydro-1H-pyrrole-2-carboxylates with methyl 2-arylamino-4-(2-naphthyl)-4-oxobut-2-enoates. Crystal and molecular structure of substituted 1,7-diazaspiro[4.4]nonane // Russian Journal of Organic Chemistry. 2014. Vol. 50. No. 7. pp. 1017-1021.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1134/S1070428014070148
UR - http://link.springer.com/10.1134/S1070428014070148
TI - Five-membered 2,3-dioxo heterocycles: CV. Reaction of methyl 1-aryl-3-aroyl-4,5-dioxo-4,5-dihydro-1H-pyrrole-2-carboxylates with methyl 2-arylamino-4-(2-naphthyl)-4-oxobut-2-enoates. Crystal and molecular structure of substituted 1,7-diazaspiro[4.4]nonane
T2 - Russian Journal of Organic Chemistry
AU - Denislamova, E S
AU - Dubovtsev, A Yu
AU - Slepukhin, P A
AU - Maslivets, A N
PY - 2014
DA - 2014/07/01
PB - Pleiades Publishing
SP - 1017-1021
IS - 7
VL - 50
SN - 1070-4280
SN - 1608-3393
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2014_Denislamova,
author = {E S Denislamova and A Yu Dubovtsev and P A Slepukhin and A N Maslivets},
title = {Five-membered 2,3-dioxo heterocycles: CV. Reaction of methyl 1-aryl-3-aroyl-4,5-dioxo-4,5-dihydro-1H-pyrrole-2-carboxylates with methyl 2-arylamino-4-(2-naphthyl)-4-oxobut-2-enoates. Crystal and molecular structure of substituted 1,7-diazaspiro[4.4]nonane},
journal = {Russian Journal of Organic Chemistry},
year = {2014},
volume = {50},
publisher = {Pleiades Publishing},
month = {jul},
url = {http://link.springer.com/10.1134/S1070428014070148},
number = {7},
pages = {1017--1021},
doi = {10.1134/S1070428014070148}
}
MLA
Cite this
MLA Copy
Denislamova, E. S., et al. “Five-membered 2,3-dioxo heterocycles: CV. Reaction of methyl 1-aryl-3-aroyl-4,5-dioxo-4,5-dihydro-1H-pyrrole-2-carboxylates with methyl 2-arylamino-4-(2-naphthyl)-4-oxobut-2-enoates. Crystal and molecular structure of substituted 1,7-diazaspiro[4.4]nonane.” Russian Journal of Organic Chemistry, vol. 50, no. 7, Jul. 2014, pp. 1017-1021. http://link.springer.com/10.1134/S1070428014070148.