@article { ISI:000321434500006,
	title = {Palladium chloride catalyzed photochemical heck reaction},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {91},
	number = {5},
	year = {2013},
	month = {MAY},
	pages = {348-351},
	publisher = {CANADIAN SCIENCE PUBLISHING, NRC RESEARCH PRESS},
	address = {65 AURIGA DR, SUITE 203, OTTAWA, ON K2E 7W6, CANADA},
	abstract = {<p>PdCl2 catalyzed carbon-carbon bond formation (Heck reaction) between substituted aryl halides and olefins was carried out without a ligand, under irradiation with UV-visible light. The results demonstrated that UV-visible light accelerated the rate of the reaction, leading to an excellent yield of corresponding products. The recovered palladium nanoparticles could be thermally recycled several times. PdCl2 gave excellent conversion up to the fifth addition of substrate.</p>},
	keywords = {C-C coupling, Heck reaction, iodobenzene, photochemical reaction},
	issn = {0008-4042},
	doi = {10.1139/cjc-2012-0377},
	author = {Waghmode, Suresh B. and Arbuj, Sudhir S. and Wani, Bina N. and Gopinath, Chinnakonda S.}
}
@article {50150,
	title = {Metal-free sustainable synthesis of oximes and hydrazones from benzyl alcohol and benzylamine},
	journal = {RSC Advances},
	volume = {16},
	year = {2026},
	month = {MAY },
	pages = {28482-28487},
	type = {Article},
	abstract = {<p>
	Herein, we report a one-pot synthesis of oximes and hydrazones via oxidative coupling of alcohols and amines with hydroxylamine hydrochloride and hydrazine, mediated by N-bromosuccinimide (NBS) and phenyliodine(iii) diacetate (PIDA), respectively. NBS mediates the benzyl alcohol oxidation, followed by coupling with hydroxylamine hydrochloride, as well as hydrazines, leading to the formation of oximes and hydrazones, respectively. Additionally, PIDA oxidizes benzylamine to the corresponding intermediate imine, which then reacts with hydroxylamine hydrochloride and hydrazine to form oximes and hydrazones, respectively. We have also demonstrated the effectiveness of this methodology through a gram-scale reaction and synthetic transformation.</p>
},
	doi = {10.1039/d6ra02204a},
	author = {Devgunde, Rupali B. and Rupanawar, Bapurao D. and Rupnavar, Prasad B. and Waghmode, Suresh B.}
}
