@article {47997,
	title = {Metal-free aminocarbonylation of p-quinone methides with isocyanides: synthesis of sterically hindered alpha-arylated acetamides},
	journal = {Chemistry-an Asian Journal},
	volume = {17},
	year = {2022},
	month = {OCT},
	pages = {e202200642},
	type = {Article},
	abstract = {<p>
	The synthesis of sterically hindered alpha-arylated acetamides generally requires a multistep reaction sequence and is also difficult to access due to steric constraints. This protocol allows the synthesis of sterically hindered alpha-arylated acetamides in moderate to high yields via 1,6-addition of isocyanides to p-quinone methides in the presence of BF3 center dot OEt2. The present transformation features transition metal-free conditions, avoiding the use of toxic carbon monoxide, broad substrate scope, mild reaction conditions, and operational simplicity.</p>
},
	keywords = {Aminocarbonylation, Isocyanide, p-Quinone methide, Sterically Hindered alpha-Arylated Acetamides},
	issn = {1861-4728},
	doi = {10.1002/asia.202200642},
	author = {Shirsath, Sachin R. and More, Devidas A. and Muthukrishnan, M.}
}
@article {48059,
	title = {Rongalite as a sulfone source: sulfonylation of para-quinone methides and alkyl/allyl halides},
	journal = {Chemistry-an Asian Journal},
	volume = {17},
	year = {2022},
	month = {AUG},
	pages = {e202200408},
	type = {Article},
	abstract = {<p>
	A one-pot three-component reaction using p-quinone methides, rongalite and alkyl/allyl halides has been described. The corresponding unsymmetrical sulfones were obtained in good yields under mild reaction conditions in the absence of any metal, base or any other additive.</p>
},
	keywords = {Alkyl halides, diaryl methine, p-Quinone methide, rongalite, sulfonylation},
	issn = {1861-4728},
	doi = {10.1002/asia.202200408},
	author = {Kale, Someshwar B. and Jori, Popat K. and Das, Utpal}
}
