Author(s):
C. Nagamani, D. Sherisha, K. Sumalatha, M. Sowjanya
Email(s):
manisunil212@gmail.com
DOI:
10.52711/0974-360X.2021.00681 
Address:
C. Nagamani1*, D. Sherisha1, K. Sumalatha1, M. Sowjanya2
1Department of Pharmaceutical Chemistry, Bhaskar Pharmacy College, Telangana, India.
2Department of Chemistry, Vijaya Teja Degree College, Addanki, Andhra Pradesh, India.
*Corresponding Author
Published In:
Volume - 14,
Issue - 7,
Year - 2021
ABSTRACT:
A set of d-amino ?-butenolides (1-5) were synthesised by a novel method using molecular iodine as a catalyst by mannich reaction. The purity and progress of the reaction was assessed by thin layer chromatography and the compounds characterisation was done by IR, proton NMR and mass spectroscopic techniques. Molecular modeling studies for the compounds such as docking was performed for the synthesized butenolides to understand the drug receptor interactions and analyze structural changes when bound to the active site of the receptor. the results showed that the compounds 2 and 3 showed significant interaction with target enzymes.
Cite this article:
C. Nagamani, D. Sherisha, K. Sumalatha, M. Sowjanya. Iodine -A Versatile reagent for Vinylogous Mannich Reaction for the Synthesis of δ-Amino γ-Butenolides and Insilico Evaluation. Research Journal of Pharmacy and Technology. 2021; 14(7):3921-6. doi: 10.52711/0974-360X.2021.00681
Cite(Electronic):
C. Nagamani, D. Sherisha, K. Sumalatha, M. Sowjanya. Iodine -A Versatile reagent for Vinylogous Mannich Reaction for the Synthesis of δ-Amino γ-Butenolides and Insilico Evaluation. Research Journal of Pharmacy and Technology. 2021; 14(7):3921-6. doi: 10.52711/0974-360X.2021.00681 Available on: https://rjptonline.org/AbstractView.aspx?PID=2021-14-7-78
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