@article { ISI:000239270000033,
	title = {Cu(OTf)(2) or Et3N-catalyzed three-component condensation of aldehydes, amines and cyanides: a high yielding synthesis of alpha-aminonitriles},
	journal = {Tetrahedron Letters},
	volume = {47},
	number = {32},
	year = {2006},
	month = {AUG},
	pages = {5759-5762},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>Copper(II) triflate or Et3N have been found to catalyze, under ambient conditions, the addition of a cyanide anion, such as trimethylsilyl cyanide or acetone cyanohydrin, onto in situ generated imines, furnishing alpha-aminonitriles in excellent yields. (c) 2006 Elsevier Ltd. All rights reserved.</p>},
	keywords = {aldehydes, aminonitriles, multicomponent reactions, organocatalyst, Strecker reaction},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2006.06.008},
	author = {Paraskar, Abhimanyu S. and Sudalai, Arumugam}
}
@article { ISI:000249771600036,
	title = {Organocatalytic activation of TMSCN by basic ammonium salts for efficient cyanation of aldehydes and imines},
	journal = {Tetrahedron Letters},
	volume = {48},
	number = {40},
	year = {2007},
	month = {OCT},
	pages = {7211-7214},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>Basic ammonium salts act as highly effective catalysts for the cyanosilylation of aldehydes and in Strecker-type aminonitrile synthesis using TMSCN as cyanide source at 25 degrees C under extremely mild conditions, affording very good to excellent yields of silylated cyanohydrins and alpha-aminonitriles. (C) 2007 Published by Elsevier Ltd.</p>},
	keywords = {aldehydes, aminonitriles, cyanohydrin, cyanosilylation, multicomponent reactions, TMSCN},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2007.07.188},
	author = {Raj, I. Victor Paul and Suryavanshi, Gurunath and Sudalai, A.}
}
