Open Access
Synthesis and anti-microbial activity of new (1-alkyl-1H-1,2,3-triazol-4-yl)methyl-2H-chromene-3-carboxylates: A click chemistry approach
Publication type: Journal Article
Publication date: 2015-07-01
scimago Q1
wos Q1
SJR: 0.939
CiteScore: 10.0
Impact factor: 5.8
ISSN: 13196103, 22124640
General Chemistry
Abstract
A series of new 1,4 disubstituted (1-alkyl-1H-1,2,3-triazol-4-yl)methyl-2H-chromene-3-carboxylates ( 4ai – 4eiii ) have been efficiently synthesized in moderate to excellent yields by the 1,3 dipolar cycloaddition between 2-propynyl-2H-chromene-3-carboxylates 3a – e and various alkyl azides under Cu(I) catalyzed conditions. The structures of the synthesized compounds are established based on IR, NMR, MASS Spectrometric methods and elemental analyses. The antibacterial and antifungal activities of synthesized compounds were evaluated. Compounds 4biii , 4ei , 4dii , 4ai , 4aii , 4bii showed good activity against bacterial strains and the compounds 4bi , 4eii against fungal strains.
Found
Nothing found, try to update filter.
Found
Nothing found, try to update filter.
Top-30
Journals
|
1
2
|
|
|
ChemistrySelect
2 publications, 22.22%
|
|
|
IOP Conference Series: Materials Science and Engineering
1 publication, 11.11%
|
|
|
Tetrahedron
1 publication, 11.11%
|
|
|
Journal of Heterocyclic Chemistry
1 publication, 11.11%
|
|
|
RSC Advances
1 publication, 11.11%
|
|
|
Organic Chemistry Frontiers
1 publication, 11.11%
|
|
|
Asian Journal of Chemistry
1 publication, 11.11%
|
|
|
Current Research in Green and Sustainable Chemistry
1 publication, 11.11%
|
|
|
1
2
|
Publishers
|
1
2
3
|
|
|
Wiley
3 publications, 33.33%
|
|
|
Elsevier
2 publications, 22.22%
|
|
|
Royal Society of Chemistry (RSC)
2 publications, 22.22%
|
|
|
IOP Publishing
1 publication, 11.11%
|
|
|
Asian Journal of Chemistry
1 publication, 11.11%
|
|
|
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
9
Total citations:
9
Citations from 2024:
1
(11%)
Cite this
GOST |
RIS |
BibTex |
MLA
Cite this
GOST
Copy
Koteswara Reddy M., Jayaprakash R. Y., David Krupadanam G. L. Synthesis and anti-microbial activity of new (1-alkyl-1H-1,2,3-triazol-4-yl)methyl-2H-chromene-3-carboxylates: A click chemistry approach // Journal of Saudi Chemical Society. 2015. Vol. 19. No. 4. pp. 372-378.
GOST all authors (up to 50)
Copy
Koteswara Reddy M., Jayaprakash R. Y., David Krupadanam G. L. Synthesis and anti-microbial activity of new (1-alkyl-1H-1,2,3-triazol-4-yl)methyl-2H-chromene-3-carboxylates: A click chemistry approach // Journal of Saudi Chemical Society. 2015. Vol. 19. No. 4. pp. 372-378.
Cite this
RIS
Copy
TY - JOUR
DO - 10.1016/j.jscs.2012.04.006
UR - https://doi.org/10.1016/j.jscs.2012.04.006
TI - Synthesis and anti-microbial activity of new (1-alkyl-1H-1,2,3-triazol-4-yl)methyl-2H-chromene-3-carboxylates: A click chemistry approach
T2 - Journal of Saudi Chemical Society
AU - Koteswara Reddy, M
AU - Jayaprakash, Rao Y
AU - David Krupadanam, G L
PY - 2015
DA - 2015/07/01
PB - King Saud University
SP - 372-378
IS - 4
VL - 19
SN - 1319-6103
SN - 2212-4640
ER -
Cite this
BibTex (up to 50 authors)
Copy
@article{2015_Koteswara Reddy,
author = {M Koteswara Reddy and Rao Y Jayaprakash and G L David Krupadanam},
title = {Synthesis and anti-microbial activity of new (1-alkyl-1H-1,2,3-triazol-4-yl)methyl-2H-chromene-3-carboxylates: A click chemistry approach},
journal = {Journal of Saudi Chemical Society},
year = {2015},
volume = {19},
publisher = {King Saud University},
month = {jul},
url = {https://doi.org/10.1016/j.jscs.2012.04.006},
number = {4},
pages = {372--378},
doi = {10.1016/j.jscs.2012.04.006}
}
Cite this
MLA
Copy
Koteswara Reddy, M., et al. “Synthesis and anti-microbial activity of new (1-alkyl-1H-1,2,3-triazol-4-yl)methyl-2H-chromene-3-carboxylates: A click chemistry approach.” Journal of Saudi Chemical Society, vol. 19, no. 4, Jul. 2015, pp. 372-378. https://doi.org/10.1016/j.jscs.2012.04.006.