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|Title:||A solid-phase equivalent of van Leusen's TosMIC, and its application in oxazole synthesis||Authors:||Kulkarni, B.A.
|Issue Date:||Jul-1999||Citation:||Kulkarni, B.A., Ganesan, A. (1999-07). A solid-phase equivalent of van Leusen's TosMIC, and its application in oxazole synthesis. Tetrahedron Letters 40 (30) : 5633-5636. ScholarBank@NUS Repository. https://doi.org/10.1016/S0040-4039(99)01049-7||Abstract:||Polystyrene-SH resin, prepared from Merrifield resin in two steps, was converted to polystyrene-SO2-CH2-NC in three steps. This resin functions as a solid-phase equivalent of p-tolylsulfonylmethyl isocyanide (TosMIC). Thus, reaction with aromatic aldehydes and tetrabutylammonium hydroxide as base yields 5-aryloxazoles.||Source Title:||Tetrahedron Letters||URI:||http://scholarbank.nus.edu.sg/handle/10635/111768||ISSN:||00404039||DOI:||10.1016/S0040-4039(99)01049-7|
|Appears in Collections:||Staff Publications|
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