@article {44497,
	title = {Identification of potent chromone embedded [1,2,3]-triazoles as novel anti-tubercular agents},
	journal = {Royal Society Open Science},
	volume = {5},
	year = {2018},
	month = {APR},
	pages = {Article Number: 171750},
	abstract = {A series of 20 novel chromone embedded [1,2,3]-triazoles derivatives were synthesized via an easy and convenient synthetic procedure starting from 2-hydroxy acetophenone. The in vitro anti-mycobacterial evaluation studies carried out in this work reveal that seven compounds exhibit significant inhibition against Mycobacterium tuberculosis H37Rv strain with MIC in the range of 1.56-12.5 mu g ml(-1). Noticeably, compound 6s was the most potent compound in vitro with a MIC value of 1.56 mu g ml(-1). Molecular docking and chemoinformatics studies revealed that compound 6s displayed drug-like properties against the enoyl-acyl carrier protein reductase of M. tuberculosis further establishing its potential as a potent inhibitor.},
	doi = {10.1098/rsos.171750},
	author = {Nalla, Viswanadh and Shaikh, Aslam and Bapat, Sanket and Vyas, Renu and Karthikeyan, M. and Yogeeswari, P. and Sriram, D. and Muthukrishnan, M.}
}
@article {47652,
	title = {Iron catalyzed tandem ring opening/1,6-conjugate addition of cyclopropanols with p-quinone methides: new access to gamma,gamma-diaryl ketones},
	journal = {Chemical Communications},
	volume = {57},
	year = {2021},
	month = {DEC },
	pages = {13582-13585},
	type = {Article},
	abstract = {An iron(iii) catalyzed tandem ring opening/1,6-conjugate addition of cyclopropanols to p-quinone methides leading to gamma,gamma-diaryl ketones has been described. This catalytic protocol provides a novel and efficient method to access gamma,gamma-diaryl ketone derivatives in good to excellent yields with high functional group tolerance. Importantly, gamma,gamma-diaryl ketone can be further functionalized to give a versatile set of useful products.},
	issn = {1359-7345},
	doi = {10.1039/d1cc05997a},
	author = {Shirsath, Sachin R. and Chandgude, Sagar M. and Muthukrishnan, M.}
}
@article {49562,
	title = {Iron mediated oxidative ring opening-homocoupling of cyclopropanols: facile access to 1,6-diketones},
	journal = {ChemistrySelect},
	volume = {10},
	year = {2025},
	month = {MAY},
	pages = {e202501745},
	type = {Article},
	abstract = {<p>
	We have developed a new approach for the synthesis of 1,6-diketones via iron-catalyzed ring opening of cyclopropanol with a nontoxic, inexpensive iron catalyst under open-air conditions. This method eliminates the need for additives and employs tert-butanol as an eco-friendly solvent. This methodology allows rapid access to a variety of symmetrical 1,6-diketones under mild conditions. Preliminary mechanistic studies revealed the involvement of radical pathways.</p>
},
	keywords = {1, 6-Diketone synthesis, C \& horbar, C bond cleavage, cyclopropanols, Homocoupling, Iron mediated},
	issn = {2365-6549},
	doi = {10.1002/slct.202501745},
	author = {Shinde, Ravi A. and Shirsath, Sachin and Muthukrishnan, M.}
}
