“…However, use of excess reagent (up to five-fold) along with toxic cyanide as the by-product limits its wide applications. [5] To further improve the scope and selectivity in reductive amination reactions, several other reducing systems including Bu 3 SnH, [6] Bu 2 SnClH and Bu 2 SnIH, [7] phenylsilane-dibutyltin dichloride, [8] and decaborane [9] have been described. All these methods require stoichiometric or excess quantities of the hydrides, which are generally highly reactive and expensive.…”