Sandeep Atkore

Dr. Sandeep Atkore

orcid

Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 October 2021 in Catalysts
Verified
Journal Article
Open access
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SASandeep Atkore
Sandeep Atkore
GBGiribala M. Bondle
Giribala M. Bondle
PRPranita Vishwanath Raithak
Pranita Vishwanath Raithak
VKVinod T. Kamble
Vinod T. Kamble
Ravi VaralaRavi Varala
Ravi Varala
Mohammed Althaf HussainMohammed Althaf Hussain
Mohammed Althaf Hussain
The synthesis of 14-aryl 14H-dibenzo[a,j]xanthenes is achieved by a simple condensation reaction between β-naphthol with aryl or alkyl aldehydes in an effective synergetic catalytic system created by combining basic bleaching earth clay and PEG-600. The advantages of the present method include catalyst recyclability, superior product yield, a shorter reaction time and the avoidance of hazardous reagents. Synthesized xanthene derivatives were also screened for their antibacterial activity against Staphylococcus aureus (MTCC 96) and Pseudomonas aeruginosa (Wild).

25 January 2022 in Bulletin of the Korean Chemical Society
Verified
Journal Article
Closed access
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MAMohammed Mujahid Alam
Mohammed Mujahid Alam
SASandeep Atkore
Sandeep Atkore
VKVinod T. Kamble
Vinod T. Kamble
Ravi VaralaRavi Varala
Ravi Varala

16 December 2021 in Asian Journal of Chemistry
Verified
Journal Article
Open access
PRPranita Vishwanath Raithak
Pranita Vishwanath Raithak
ADArvind S. Dhabe
Arvind S. Dhabe
SASandeep Atkore
Sandeep Atkore
MAMohammed Mujahid Alam
Mohammed Mujahid Alam
VKVIJAY KOTRA
VIJAY KOTRA
Ravi VaralaRavi Varala
Ravi Varala
A series of novel indole quinoline derived chalcones were synthesized using cost-effective synergetic catalytic system consisting of heterogeneous basic bleaching earth clay (pH 12.5) and PEG-400 as solvent at ambient temperature with the yields of 60-76%. All these chalcones were characterized by spectral data. Both the DPPH and SOR scavenging assays were performed to evaluate their antioxidant nature of these compounds.

13 February 2017 in Letters in Organic Chemistry
Verified
Journal Article
Closed access
GBGiribala Bondle
Giribala Bondle
RJRohit Jadhav
Rohit Jadhav
VKVinod Kamble
Vinod Kamble
SASandeep Atkore
Sandeep Atkore
Background: 1,3,5-Hexahydrotriazine derivatives show broad spectrum of biological activities such as anticancer, antitumor. Some of their derivatives are used as carcenolytics, herbicides and show antidote and growth stimulating activities. Very few methodologies are reported for the synthesis of symtriazines. Synthesis of trimer of hexahydrotriazines is pH sensitive reaction and instead of using any acidic and basic conditions, we tried to synthesize this trimer under neutral conditions. Methods: Synthesis of 1,3,5-hexahydro symtriazine derivatives has been achieved by treating parasubstituted aniline with solution of paraformaldehyde using PEG-400 as neutral medium using grindstone method. Results: Symtriazine derivatives were synthesized in good to excellent yields (95-70%) within a short time of 5-7 minutes by grindstone technique using PEG-400 as neutral solvent medium. All the synthesized compounds were characterized by 1HNMR, 13CNMR, Mass and Melting point. Conclusion: This is the first report for the synthesis of 1,3,5-hexahydro-sym-triazine trimer starting from aniline/substituted aniline and paraformaldehyde in the presence of reusable and environmental friendly solvent media PEG-400 by grindstone technique.