@article { ISI:000309787500006,
	title = {Ligand promoted and controlled palladium-catalyzed intramolecular Heck reaction of homoallyl alcohols: a facile synthesis of cyclopentaannulated quinolines},
	journal = {Tetrahedron},
	volume = {68},
	number = {45},
	year = {2012},
	month = {NOV},
	pages = {9206-9210},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>Bidentate phosphine ligands in palladium-catalyzed intramolecular Heck reactions of 2-chloroquinolin-3-yl-(1-homoallyl)alcohols are described to afford facile synthesis of 3-methylene-2,3-dihydro-1H-cy-clopenta[b]quinolines in improved yields. We further observed using bulky aromatic phosphine ligand in Pd-catalyzed intermolecular Heck coupling reaction at olefinic centers with iodobenzene also favored exclusively Heck products in excellent yield. (C) 2012 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Heck cyclization, Homoallyl alcohol, Ligand promoted, Palladium-catalyzed, Quinoline},
	issn = {0040-4020},
	doi = {10.1016/j.tet.2012.08.088},
	author = {Singh, Radhey M. and Chandra, Atish and Sharma, Neha and Singh, Bhawana and Kumar, Ritush}
}
@article {44124,
	title = { p-Selective (sp(2))-C-H functionalization for an acylation/alkylation reaction using organic photoredox catalysis},
	journal = { Chemical Communications},
	volume = {53},
	year = {2017},
	month = {NOV},
	pages = {12337-12340},
	type = {Article},
	abstract = {p-Selective (sp(2))-C-H functionalization of electron rich arenes has been achieved for acylation and alkylation reactions, respectively, with acyl/alkylselenides by organic photoredox catalysis involving an interesting mechanistic pathway.},
	doi = {10.1039/c7cc07529d},
	author = {Pandey, Ganesh and Tiwari, Sandip Kumar and Singh, Bhawana and Vanka, Kumar and Jain, Shailja}
}
