@article {48296, title = {Ultrasound assisted synthesis of spirooxindolo-1,2,4-oxadiazoles via [3+2] cycloaddition reaction and their anti-cancer activity}, journal = {ARKIVOC}, year = {2023}, month = {MAY}, pages = {S1-S46}, type = {Article}, issn = {1551-7004}, author = {Kanchrana, Madhu and Allaka, Bhargava Sai and Krishna, Gamidi Rama and Basavoju, Srinivas} } @article {49343, title = {Design, synthesis, anti-mycobacterial activity, molecular docking and ADME analysis of spiroquinoxaline-1,2,4-oxadiazoles via [3+2] cycloaddition reaction under ultrasound irradiation}, journal = {MOLECULAR DIVERSITY}, volume = {28}, year = {2024}, month = {DEC 2024}, pages = {3979-3991}, type = {Journal Article}, keywords = {2, 4-oxadiazoles, cytotoxicity activity, molecular, Mycobacterium tuberculosis, Spiroquinoxaline-1}, issn = {1381-1991}, doi = {10.1007/s11030-023-10790-9}, author = {Kanchrana, Madhu and Gamidi, Rama Krishna and Kumari, Jyothi and Sriram, Dharmarajan and Basavoju, Srinivas} } @article {49368, title = {Ionic liquid assisted green synthesis of quinoxaline based bisspirooxindoles: anticancer evaluation and molecular dynamics}, journal = {CHEMISTRYSELECT}, volume = {9}, year = {2024}, month = {NOV}, pages = {e202403608}, type = {Journal Article}, keywords = {Cycloaddition, spirooxindoles}, issn = {2365-6549}, doi = {10.1002/slct.202403608}, author = {Kanchrana, Madhu and Krishna, Gamidi Rama and Dey, Biswajit and Pandey, Nandita and Guru, Santosh Kumar and Sangolkar, Akanksha Ashok and Pawar, Ravinder and Basavoju, Srinivas} } @article {49646, title = { Synthesis of quinazolinone based spirocyclopropanes via [3?+?2] cycloaddition reaction: in silico anti-tubercular molecular docking studies and ADME prediction}, journal = {Polycyclic Aromatic Compounds}, volume = {44}, year = {2024}, month = {SEP}, type = {Article}, abstract = {

A highly efficient cascade annulation approach is developed for the synthesis of novel quinazolinone-based spirocyclopropanes\ via\ three-component [3 + 2] cycloaddition reaction with aldehydes, tosylhydrazide and quinazolinyl chalcones. The reaction features the formation of two C{\textendash}C bonds and three stereogenic centers. A variety of highly functionalized spirocyclopropyl quinazolinones were obtained in good yields under mild reaction conditions. Furthermore,\ in silico\ anti-tubercular (anti-TB) molecular docking studies were performed for the generated compounds against three Mycobacterium tuberculosis proteins with PDBID: 1DF7, 1P44 and 4TZK. ADME prediction were evaluated for the drug like properties of the synthesized compounds.

}, doi = {https://doi.org/10.1080/10406638.2023.2257838}, author = {Allaka, Bhargava Sai and Kanchrana, Madhu and Gamidi, Rama Krishna and Basavoju, Srinivas} }