2014
DOI: 10.4236/ijoc.2014.45031
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Simple Reduction of Hydantoins with Sodium Borohydride

Abstract: The reduction of various hydantoins with sodium borohydride gave the corresponding 4-hydroxy-2-imidazolidinones in high yields. In contrast, reduction employing a boron trifluoride etheratesodium borohydride system generated 2-imidazolidinones. In both reductions, the reactivity of the hydantoin was dependent on its substituents. The Lewis acid-promoted reactions of a 4-hydroxy-2-imidazolidinone with nucleophiles were also investigated.

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“…The imidazolidine is five-membered heterocycles containing two nitrogen atoms [1]. N-heterocyclic carbine (NHC)-derived complexes have been used as powerful catalysts for effecting many transformations [2].…”
Section: Introductionmentioning
confidence: 99%
“…The imidazolidine is five-membered heterocycles containing two nitrogen atoms [1]. N-heterocyclic carbine (NHC)-derived complexes have been used as powerful catalysts for effecting many transformations [2].…”
Section: Introductionmentioning
confidence: 99%