@article { ISI:000346134300012,
	title = {Continuous-flow meerwein arylation},
	journal = {Journal of Flow Chemistry},
	volume = {4},
	number = {4},
	year = {2014},
	month = {DEC},
	pages = {211-216},
	publisher = {AKADEMIAI KIADO RT},
	type = {Article},
	address = {PRIELLE K U 19, PO BOX 245,, H-1117 BUDAPEST, HUNGARY},
	abstract = {<p>The continuous-flow Meerwein arylation is demonstrated for a set of few aryl donors (anilines and m-aminoacetophenone) and specific radical acceptors. Homogeneous catalyst (CuBr in HBr and CuCl in HCl) was used to facilitate the reaction. The effect of parameters, viz., temperature, catalyst concentration, residence time, and concentration of the radical acceptor on the yield of the arylated product, was studied. The yield of the aryl derivative obtained by continuous-flow syntheses was always better than the respective experiments in batch mode. Flow synthesis allows easy variation in these parameters and thus allows going close to the maximum possible yields in a system where the relative rates of different reactions create a complex situation. Temperature plays a crucial role by affecting the rates as well as by governing the system homogeneity. The nitrogen bubbles generated in the reaction helped to avoid any channel blockage.</p>},
	keywords = {diazonium salt, flow chemistry, homogeneous catalyst, Meerwein arylation, micromixer, multistep synthesis},
	issn = {2062-249X},
	doi = {10.1556/JFC-D-14-00023},
	author = {Bhaya, Vinay G. and Joshi, Ramesh A. and Kulkarni, Amol A.}
}
@article {49314,
	title = {Accessing meta -enone-substituted anisoles using ArN 2 BF 4 as precatalyst via rearrangement of alkyne-tethered cyclohexadienones},
	journal = {Synthesis-Stuttgart},
	volume = {56},
	year = {2024},
	month = {AUG },
	pages = {2499-2506},
	type = {Article},
	keywords = {alkyne-tethered cyclohexadienone, diazonium salt, rearrangement, substituted anisoles},
	issn = {0039-7881},
	doi = {10.1055/a-2331-9439},
	author = {Rai, Archana and Das, Utpal}
}
