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Requested Article:
Hexahydrospiro‐pyrazolo[3,4‐b]pyridine‐4,1′‐pyrrolo[3,2,1‐ij]quinolines Derived from 5,6‐dihydro‐4H‐pyrrolo[3,2,1‐ij]quinoline‐1,2‐dione
Bahman Ebrahimi Saatluo, Mehdi M. Baradarani, J. A. Joule
Journal of Heterocyclic Chemistry (2018) Vol. 55, Iss. 5, pp. 1176-1182
Closed Access | Times Cited: 11
Bahman Ebrahimi Saatluo, Mehdi M. Baradarani, J. A. Joule
Journal of Heterocyclic Chemistry (2018) Vol. 55, Iss. 5, pp. 1176-1182
Closed Access | Times Cited: 11
Showing 11 citing articles:
Multicomponent Reactions Using C,N-Binucleophilic Nature of Aminopyrazoles: Construction of Pyrazole-Fused Heterocycles
Tasneem Parvin
Topics in Current Chemistry (2023) Vol. 381, Iss. 4
Closed Access | Times Cited: 8
Tasneem Parvin
Topics in Current Chemistry (2023) Vol. 381, Iss. 4
Closed Access | Times Cited: 8
The Study of Reaction of Hexafluoro‐1,4‐Napthoquinone With Substituted 5‐Aminopyrazoles
Ekaterina Kudryavtseva, Boris V. Lichitsky, Andrey N. Komogortsev, et al.
Journal of Heterocyclic Chemistry (2024)
Closed Access | Times Cited: 2
Ekaterina Kudryavtseva, Boris V. Lichitsky, Andrey N. Komogortsev, et al.
Journal of Heterocyclic Chemistry (2024)
Closed Access | Times Cited: 2
Arylformylacetonitriles in Multicomponent Reactions Leading to Heterocycles
Yuan Zhong
European Journal of Organic Chemistry (2022) Vol. 2022, Iss. 48
Closed Access | Times Cited: 6
Yuan Zhong
European Journal of Organic Chemistry (2022) Vol. 2022, Iss. 48
Closed Access | Times Cited: 6
New hybrid compounds bearing pyrrolo[3,2,1-ij]quinolin-2-one and coumarin motifs. Synthesis and evaluation of anticoagulant activity
A. A. Skoptsova, N. P. Novichikhina, E. A. Kosheleva, et al.
Russian Chemical Bulletin (2023) Vol. 72, Iss. 12, pp. 2898-2907
Closed Access | Times Cited: 3
A. A. Skoptsova, N. P. Novichikhina, E. A. Kosheleva, et al.
Russian Chemical Bulletin (2023) Vol. 72, Iss. 12, pp. 2898-2907
Closed Access | Times Cited: 3
Synthesis of Hexahydrospiro[pyrazolo[3,4‐b]quinoline‐4,1′‐pyrrolo[3,2,1‐ij]quinoline‐2′,5(1H,4′H)‐diones] from 5,6‐dihydro‐4H‐pyrrolo[3,2,1‐ij]quinoline‐1,2‐dione Using Fe3O4@Cu(OH)x as a Nanocatalyst
Mehdi M. Baradarani, Bahman Ebrahimi Saatluo, Shiva Ghabeli, et al.
Journal of Heterocyclic Chemistry (2019) Vol. 56, Iss. 7, pp. 1999-2007
Closed Access | Times Cited: 4
Mehdi M. Baradarani, Bahman Ebrahimi Saatluo, Shiva Ghabeli, et al.
Journal of Heterocyclic Chemistry (2019) Vol. 56, Iss. 7, pp. 1999-2007
Closed Access | Times Cited: 4
Synthesis of polycyclic 3,3′-spirooxindoles and some new 2-arylquinoxalines from (E/Z)- 1-(2-oxo-2-arylethylidene)-5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-2(1H)-ones
Bahman Ebrahimi Saatluo, Ruhollah Amanollahi, Hadi Zare Fazlelahi, et al.
Journal of Molecular Structure (2022) Vol. 1255, pp. 132445-132445
Closed Access | Times Cited: 3
Bahman Ebrahimi Saatluo, Ruhollah Amanollahi, Hadi Zare Fazlelahi, et al.
Journal of Molecular Structure (2022) Vol. 1255, pp. 132445-132445
Closed Access | Times Cited: 3
New complex polycyclic compounds: Synthesis, antiproliferative activity and mechanism of action
Giuseppe Daidone, Antonella D’Anneo, Maria Valeria Raimondi, et al.
Bioorganic Chemistry (2020) Vol. 101, pp. 103989-103989
Closed Access | Times Cited: 3
Giuseppe Daidone, Antonella D’Anneo, Maria Valeria Raimondi, et al.
Bioorganic Chemistry (2020) Vol. 101, pp. 103989-103989
Closed Access | Times Cited: 3
Synthesis and Study of New Anticoagulant Candidates Based on 6-Aryl-5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1,2-diones
A. A. Skoptsova, N. P. Novichikhina, E. A. Kosheleva, et al.
Russian Journal of General Chemistry (2023) Vol. 93, Iss. S1, pp. S115-S123
Closed Access | Times Cited: 1
A. A. Skoptsova, N. P. Novichikhina, E. A. Kosheleva, et al.
Russian Journal of General Chemistry (2023) Vol. 93, Iss. S1, pp. S115-S123
Closed Access | Times Cited: 1
Synthesis of New 1-Hydroxy-4H-pyrrolo[3,2,1-ij]quinolin-2(1H)-one Derivatives
N. P. Novichikhina, А. С. Шестаков, A. A. Skoptsova, et al.
Russian Journal of Organic Chemistry (2021) Vol. 57, Iss. 10, pp. 1592-1599
Closed Access | Times Cited: 2
N. P. Novichikhina, А. С. Шестаков, A. A. Skoptsova, et al.
Russian Journal of Organic Chemistry (2021) Vol. 57, Iss. 10, pp. 1592-1599
Closed Access | Times Cited: 2
Three-component synthesis of novel spiro[4H-pyran-3,3′-oxindoles] using 5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinoline-1,2-dione
Parvin Zafari, Bahman Ebrahimi Saatluo, Ahmad Rashidi, et al.
ARKIVOC (2020) Vol. 2021, Iss. 2, pp. 9-16
Open Access | Times Cited: 1
Parvin Zafari, Bahman Ebrahimi Saatluo, Ahmad Rashidi, et al.
ARKIVOC (2020) Vol. 2021, Iss. 2, pp. 9-16
Open Access | Times Cited: 1
Bicyclic 5-6 Systems: Three Heteroatoms 2:1
János Sápi, Stéphane Gérard
Elsevier eBooks (2020), pp. 212-382
Closed Access
János Sápi, Stéphane Gérard
Elsevier eBooks (2020), pp. 212-382
Closed Access