volume 93 issue 5 pages 1274-1293

Development of Spiro[chromane-2,4′-piperidine]-4(3H)-one Compounds in the Field of Medicinal Chemistry Research (A Review)

Sabyasachi Banerjee 1
Subhasis Banerjee 1
U. Chakraborty 2
S. Banerjee 2
Sourav De 3
S.K. Pranav Kumar 4
1
 
Department of Pharmaceutical Chemistry, Gupta College of Technological Sciences, Asansol, India
2
 
Department of Pharmacology, Gupta College of Technological Sciences, Asansol, India
Publication typeJournal Article
Publication date2023-05-01
scimago Q4
wos Q4
SJR0.179
CiteScore1.4
Impact factor0.8
ISSN10703632, 16083350
General Chemistry
Abstract
In the recent past, spiro[chromane-2,4′-piperidine]-4(3H)-one has been proven as one of the most valued scaffolds utilized by several medicinal chemists and pharmacologists to yield therapeutically effective biologicals. Spiro[chromane-2,4′-piperidine]-4(3H)-one is a member of the six-membered tricyclic molecule containing oxygen and nitrogen as hetero atoms. A spiro compounds is usually formed by the simultaneous reactions of condensation and cyclization. Owing to its versatile features, it has been incorporated in a wide variety of pharmaceuticals, bio-chemicals, sometimes even in the generation of hits as well as lead molecules. Chromanone-based spiro compounds have garnered a great deal of attention in recent years due to their presence in biologically active naturally derived compounds, such as vitamins, alkaloids, hormones, antibiotics, glycosides, and several other products. Compounds with the said backbone have shown their pharmacological potential as antidiabetic, anticancer, antioxidant, anti-inflammatory, anti-obesity, antihypertensive, antiplasmodial, antimalarial and antitumor. In addition to these, over the past few years, significant advancements in complex amido-piperidyl linked spiro heterocyclic chroman-4-ones have been continuously reported in pre-clinical and clinical investigations. This investigation highlights the remarkable development in the synthesis of spiro[chromane-2,4′-piperidine]-4(3H)-one-derived compounds over the past several years while focusing on the aspects of their therapeutical importance. In few cases plausible synthetic mechanism was also discussed.
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Banerjee S. et al. Development of Spiro[chromane-2,4′-piperidine]-4(3H)-one Compounds in the Field of Medicinal Chemistry Research (A Review) // Russian Journal of General Chemistry. 2023. Vol. 93. No. 5. pp. 1274-1293.
GOST all authors (up to 50) Copy
Banerjee S., Banerjee S., Chakraborty U., Banerjee S., De S., Pranav Kumar S. Development of Spiro[chromane-2,4′-piperidine]-4(3H)-one Compounds in the Field of Medicinal Chemistry Research (A Review) // Russian Journal of General Chemistry. 2023. Vol. 93. No. 5. pp. 1274-1293.
RIS |
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RIS Copy
TY - JOUR
DO - 10.1134/s1070363223050274
UR - https://doi.org/10.1134/s1070363223050274
TI - Development of Spiro[chromane-2,4′-piperidine]-4(3H)-one Compounds in the Field of Medicinal Chemistry Research (A Review)
T2 - Russian Journal of General Chemistry
AU - Banerjee, Sabyasachi
AU - Banerjee, Subhasis
AU - Chakraborty, U.
AU - Banerjee, S.
AU - De, Sourav
AU - Pranav Kumar, S.K.
PY - 2023
DA - 2023/05/01
PB - Pleiades Publishing
SP - 1274-1293
IS - 5
VL - 93
SN - 1070-3632
SN - 1608-3350
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2023_Banerjee,
author = {Sabyasachi Banerjee and Subhasis Banerjee and U. Chakraborty and S. Banerjee and Sourav De and S.K. Pranav Kumar},
title = {Development of Spiro[chromane-2,4′-piperidine]-4(3H)-one Compounds in the Field of Medicinal Chemistry Research (A Review)},
journal = {Russian Journal of General Chemistry},
year = {2023},
volume = {93},
publisher = {Pleiades Publishing},
month = {may},
url = {https://doi.org/10.1134/s1070363223050274},
number = {5},
pages = {1274--1293},
doi = {10.1134/s1070363223050274}
}
MLA
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Banerjee, Sabyasachi, et al. “Development of Spiro[chromane-2,4′-piperidine]-4(3H)-one Compounds in the Field of Medicinal Chemistry Research (A Review).” Russian Journal of General Chemistry, vol. 93, no. 5, May. 2023, pp. 1274-1293. https://doi.org/10.1134/s1070363223050274.