Please use this identifier to cite or link to this item:
https://doi.org/10.1016/S0040-4039(99)01049-7
DC Field | Value | |
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dc.title | A solid-phase equivalent of van Leusen's TosMIC, and its application in oxazole synthesis | |
dc.contributor.author | Kulkarni, B.A. | |
dc.contributor.author | Ganesan, A. | |
dc.date.accessioned | 2014-11-28T02:49:28Z | |
dc.date.available | 2014-11-28T02:49:28Z | |
dc.date.issued | 1999-07 | |
dc.identifier.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 | |
dc.identifier.issn | 00404039 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/111768 | |
dc.description.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. | |
dc.description.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/S0040-4039(99)01049-7 | |
dc.source | Scopus | |
dc.subject | Combinatorial chemistry | |
dc.subject | Isocyanides | |
dc.subject | Oxazoles | |
dc.subject | Solid-phase synthesis | |
dc.type | Article | |
dc.contributor.department | INSTITUTE OF MOLECULAR & CELL BIOLOGY | |
dc.description.doi | 10.1016/S0040-4039(99)01049-7 | |
dc.description.sourcetitle | Tetrahedron Letters | |
dc.description.volume | 40 | |
dc.description.issue | 30 | |
dc.description.page | 5633-5636 | |
dc.description.coden | TELEA | |
dc.identifier.isiut | 000081427400050 | |
Appears in Collections: | Staff Publications |
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