@article {46157,
	title = {Metal-free, radical 1,6-conjugated addition of cyclic ethers with para-quinone methides (p-QMs)},
	journal = {Organic \& Biomolecular Chemistry},
	volume = {17},
	year = {2019},
	month = {MAR},
	pages = {3239-3248},
	type = {Article},
	abstract = {<p>An efficient method for metal-free C-C bond formation between p-quinone methides (p-QMs) and cyclic ethers via a radical pathway to afford substituted diarylmethanes and triarylmethanes or to effect the -alkylation of the cyclic ethers has been developed. Also, the synthesis of 3,3-disubstituted oxindoles with stereogenic quaternary carbon centers was successfully achieved under mild reaction conditions.</p>
},
	issn = {1477-0520},
	doi = {10.1039/c9ob00127a},
	author = {More, Satish G. and Suryavanshi, Gurunath}
}
@article {47640,
	title = {Metal-free, acid-catalyzed 1,6-conjugate addition of NH-sulfoximines to para-quinone methides: accessing to diarylmethine imino sulfanone},
	journal = {Journal of Organic Chemistry},
	volume = {86},
	year = {2021},
	month = {AUG },
	pages = {10129-10139},
	type = {Article},
	abstract = {We have reported an efficient and metal-free method for the construction of alpha-diarylmethine imino sulfanone using acid-catalyzed 1,6-conjugate addition of sulfoximines on para-quinine methides (p-QMs). This method showed broad functional group tolerance and a wide range of substrate scope with good to excellent yield. The excellent protocol exhibits mild reaction conditions with high atom economy. The practicability of the present method was supported by a Gram-scale reaction.},
	issn = {0022-3263},
	doi = {10.1021/acs.joc.1c00869},
	author = {More, Satish G. and Rupanawar, Bapurao D. and Suryavanshi, Gurunath}
}
@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}
}
