@article {48024,
	title = {Metal-free access to hindered N-alkyl sulfoximines via in-situ generated Aza-oxyallyl cations from functionalized alkyl bromide},
	journal = {Asian Journal of Organic Chemistry},
	volume = {11},
	year = {2022},
	month = {JUL},
	pages = {e202200210},
	type = {Article},
	abstract = {<p>
	Herein, we report a catalyst-free and mild synthetic method for the construction of hindered N-alkyl sulfoximines derivative. A wide range of hindered di-alkyl sulfoximines can be readily obtained from the reaction of alpha-bromo-hydroxamates with a variety of sulfoximines, including diaryl, aryl-alkyl, di-alkyl and heteroaryl sulfoximines.</p>
},
	keywords = {alpha-Bromo hydroxamates, Aza-oxyallyl cations, Di-alkyl sulfoximines, metal-free, Sulfoximines},
	issn = {2193-5807},
	doi = {10.1002/ajoc.202200210},
	author = {More, Satish G. and Mane, Kishor D. and Suryavanshi, Gurunath}
}
