@article {47496,
	title = {Efficient and cost effective synthesis of acetamides catalyzed by calcium chloride},
	journal = {Indian Journal of Chemistry Section B-Organic Chemistry Including Medicinal Chemistry},
	volume = {58},
	year = {2019},
	month = {OCT},
	pages = {1125-1130},
	type = {Article},
	abstract = {CaCl2 has been found to be an efficient and cost effective catalyst for the rapid synthesis of acetamides in high yields. The use of stoichiometric quantities of acetic anhydride under solvent free conditions without any additional chromatographic purifications makes this protocol a safe alternative to the existing methods.},
	keywords = {Acetamide, acetylation, Acylation, Amine, CaCl2},
	issn = {0376-4699},
	author = {Sangole, M. T. and Thorat, S. M. and Shirsath, S. and Deshmukh, S. P. and Muthukrishnan, M. and Mujahid, M.}
}
@article {46312,
	title = {Efficient synthesis of optically active neolignans ligraminol D and E},
	journal = {Synthesis-Stuttgart},
	volume = {51},
	year = {2019},
	month = {NOV},
	pages = {4291-4295},
	type = {Article},
	abstract = {<p>Efficient syntheses of optically active neolignans ligraminol D and E were achieved in four simple steps starting from easily available chiral benzyl glycidyl ethers. The products were obtained in good overall yields and high enantioselectivities. The protocol might also be useful in the synthesis of other ligraminols or related neolignans.</p>
},
	keywords = {benzyl glycidyl ether, Epoxide, lignan, ligraminol, Mitsunobu},
	issn = {0039-7881},
	doi = {10.1055/s-0037-1611919},
	author = {Ghotekar, Ganesh S. and Mujahid, M. and Muthukrishnan, M.}
}
@article {49881,
	title = {Efficient Copper-Catalyzed, One-Pot Synthesis of N2-Aryl Phosphoryl 1,2,3-Triazole 1-Oxides},
	journal = {Asian Journal of Organic Chemistry},
	volume = {14},
	year = {2025},
	month = {OCT},
	pages = {e00162},
	type = {Article},
	abstract = {<p>
	A simple and facile one-pot process has been developed for the synthesis of N 2-aryl phosphoryl 1,2,3-triazole 1-oxide derivatives. This new approach utilizes simple and commercially available starting materials, operating under mild conditions. The method employs copper-catalyzed multicomponent reaction, involving the combination of arylhydrazines, beta-ketophosphonates, and tert-butyl nitrite. The developed protocol shows excellent functional group tolerance permitting an extensive range of substrate scope up to 92\% isolated yield.</p>
},
	keywords = {Copper-catalyzed, Phosphoryl triazoles N-oxides, Phosphorylated compound, Triazole N-oxides},
	issn = {2193-5807},
	doi = {10.1002/ajoc.202500162},
	author = {Mujahid, M. and Bhavar, Akshay A. and Vara, Vijay and Gonnade, Rajesh and Muthukrishnan, M.}
}
