@article { ISI:000299582200011,
	title = {Pd-catalyzed selective hydrosilylation of aryl ketones and aldehydes},
	journal = {Tetrahedron Letters},
	volume = {53},
	number = {2},
	year = {2012},
	month = {JAN},
	pages = {148-150},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>Pd salts in combination with triethylsilane as hydride source and DMF as solvent has been found to be excellent catalytic combination that selectively reduces aryl ketones and aldehydes under mild conditions to afford triethylsilyloxy compounds in excellent yields. Product selectivity to the respective benzyl alcohols can however be achieved when the reaction was performed in DMF/H2O (4:1) as solvent system. (C) 2011 Elsevier Ltd. All rights reserved.</p>},
	keywords = {aldehydes, Hydrosilylation, Ketones, Palladium, Triethylsilane},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2011.10.155},
	author = {Chouthaiwale, Pandurang V. and Rawat, Varun and Sudalai, Arumugam}
}
@article { ISI:000318917000003,
	title = {Proline catalyzed sequential alpha-aminooxylation or -amination/reductive cyclization of o-nitrohydrocinnamaldehydes: a high yield synthesis of chiral 3-substituted tetrahydroquinolines},
	journal = {Organic \& Biomolecular Chemistry},
	volume = {11},
	number = {22},
	year = {2013},
	month = {APR},
	pages = {3608-3611},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>A new sequential organocatalytic method for the synthesis of chiral 3-substituted (X = OH, NH2) tetrahydroquinoline derivatives (THQs) [ee up to 99\%, yield up to 87\%] based on alpha-aminooxylation or -amination followed by reductive cyclization of o-nitrohydrocinnamaldehydes has been described. This methodology has been efficiently demonstrated in the synthesis of two important bioactive molecules namely (-)-sumanirole (96\% ee) and 1-[(S)-3-(dimethylamino)-3,4-dihydro-6,7-dimethoxy-quinolin-1(2H)-yl]- propanone (92\% ee).</p>},
	issn = {1477-0520},
	doi = {10.1039/c3ob40320c},
	author = {Rawat, Varun and Kumar, B. Senthil and Sudalai, Arumugam}
}
