Synthesis of polyamide containing optically active thymine derivative as a grafted pendant
dc.contributor.author | Lu, Chengxun | en_US |
dc.contributor.author | Ji, Aixue | en_US |
dc.contributor.author | Overberger, Charles Gilbert | en_US |
dc.date.accessioned | 2006-04-28T18:18:03Z | |
dc.date.available | 2006-04-28T18:18:03Z | |
dc.date.issued | 1986-02 | en_US |
dc.identifier.citation | Lu, C. X.; Ji, Aixue; Overberger, C. G. (1986)."Synthesis of polyamide containing optically active thymine derivative as a grafted pendant." Journal of Polymer Science Part A: Polymer Chemistry 24(2): 269-278. <http://hdl.handle.net/2027.42/38819> | en_US |
dc.identifier.issn | 0887-624X | en_US |
dc.identifier.issn | 1099-0518 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/38819 | |
dc.description.abstract | A new route to polyamides containing optically active thymine groups as pendants has been established. The method is based on the grafting of (–) and (±)-2-(thymin-1-yl)propionic acid [(–) and (±) TPA] onto a polyamide containing hydroxyl groups. The hydroxy polyamide was prepared by selective N -acylation of an active diester of N -hydroxy-5-norborene-2,3-dicarboxamide (HONB), N , N '-(isophthaloyl-dioxy)-bis(5-norbornene-2,3-dicarboximide) (IPBONB), with 1,3-diamino-2-hydroxypropane (AHP). Model compounds (−) and (±)-(1,3-dibenzoylamino-2-propyl)2-(thymin-1-yl)propionate[(−) and (±) (BAPTP)] were prepared by direct, low-temperature esterification before synthesizing the polymer. | en_US |
dc.format.extent | 457480 bytes | |
dc.format.extent | 3118 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.language.iso | en_US | |
dc.publisher | John Wiley & Sons, Inc. | en_US |
dc.subject.other | Chemistry | en_US |
dc.subject.other | Polymer and Materials Science | en_US |
dc.title | Synthesis of polyamide containing optically active thymine derivative as a grafted pendant | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Chemical Engineering | en_US |
dc.subject.hlbtoplevel | Engineering | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Chemistry and the Macromolcular Research Center, The University of Michigan, Ann Arbor, MI 48109 | en_US |
dc.contributor.affiliationum | Department of Chemistry and the Macromolcular Research Center, The University of Michigan, Ann Arbor, MI 48109 | en_US |
dc.contributor.affiliationum | Department of Chemistry and the Macromolcular Research Center, The University of Michigan, Ann Arbor, MI 48109 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/38819/1/080240206_ftp.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1002/pola.1986.080240206 | en_US |
dc.identifier.source | Journal of Polymer Science Part A: Polymer Chemistry | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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