Please use this identifier to cite or link to this item: https://doi.org/10.1021/jo962376u
Title: Solution-phase synthesis of a combinatorial thiohydantoin library
Authors: Sim, M.M. 
Ganesan, A. 
Issue Date: 1997
Citation: Sim, M.M., Ganesan, A. (1997). Solution-phase synthesis of a combinatorial thiohydantoin library. Journal of Organic Chemistry 62 (10) : 3230-3235. ScholarBank@NUS Repository. https://doi.org/10.1021/jo962376u
Abstract: An efficient one-pot three-component synthesis of thiohydantoins was developed. In the first step, amino acid esters were alkylated by imine formation with aldehydes and reduction by sodium triacetoxyborohydride. In the second step, an isothiocyanate was added together with a molar equivalent of triethylamine, leading to the thiohydantoin product in high yield and purity after an extractive aqueous workup. This procedure was used to generate a combinatorial library of over 600 discrete thiohydantoins on a 0.1 mmol scale. Sampling of 10% of this library showed the thiohydantoin to be the major product in all cases, with purities of 52-98% by HPLC analysis. The cyclization conditions can also be adapted to the synthesis of hydantoins.
Source Title: Journal of Organic Chemistry
URI: http://scholarbank.nus.edu.sg/handle/10635/116598
ISSN: 00223263
DOI: 10.1021/jo962376u
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