@article {42759,
	title = {Suzuki cross-coupling reactions catalyzed by palladium complex of an inexpensive phosphinite, 2-diphenylphosphinoxynaphthyl},
	journal = {Journal of Molecular Catalysis A-Chemical},
	volume = {259},
	year = {2006},
	month = {NOV},
	pages = {78{\textendash}83},
	type = {Article},
	abstract = {<p>A facile and less expensive monophosphinite ligand 2-(diphenylphosphinoxy)-naphthyl, C10H7OPPh2 (1) has been synthesized from the reaction of β-naphthol with chlorodiphenylphosphine. The mixture of Pd(OAc)2 and 1 catalyzes the Suzuki cross-coupling of a variety of aryl halides with aryl boronic acids at room temperature or at 60 {\textdegree}C, giving generally high yields even under low catalytic loads. The effect of solvent, base and catalyst loading on the coupling reaction of aryl halide with arylboronic acid is also described.</p>},
	doi = {10.1016/j.molcata.2006.05.067},
	author = {Punji, Benudhar and Ganesamoorthy, Chelladurai and Balakrishna, Maravanji S.}
}
@article {42750,
	title = {O-2-Naphthyl diphenylthiophosphinate},
	journal = {Acta Crystallographica Section E-Crystallographic Communications},
	volume = {63},
	year = {2007},
	month = {DEC},
	pages = {4644},
	type = {Article},
	abstract = {<p>The mol-ecule of the title compound, C10H7OP(S)(C6H5)2 or C22H17OPS, exhibits distorted tetra-hedral geometry about the P atom. The P=S bond of 1.9355 (4) {\r A} is shorter than that found in Ph3P=S [1.950 (3) {\r A}] because the replacement of one carbon on phospho-rus by oxygen increases the effective electronegativity of the P atom, thereby enhancing pπ{\textendash}dπ back-donation from a lone-pair orbital of the S atom.</p>},
	doi = {10.1107/S1600536807056127},
	author = {Mague, Joel T. and Punji, Benudhar and Ganesamoorthy, Chelladurai and Balakrishna, Maravanji S.}
}
