A novel method for the synthesis of 6,7-unsubstituted pyrrolo[3,2-]pyrimidines
dc.contributor.author | Cupps, Thomas L. | en_US |
dc.contributor.author | Wise, Dean S. | en_US |
dc.contributor.author | Townsend, Leroy B. | en_US |
dc.date.accessioned | 2006-04-07T17:58:35Z | |
dc.date.available | 2006-04-07T17:58:35Z | |
dc.date.issued | 1982 | en_US |
dc.identifier.citation | Cupps, Thomas L., Wise, Dean S., Townsend,, Leroy B. (1982)."A novel method for the synthesis of 6,7-unsubstituted pyrrolo[3,2-]pyrimidines." Tetrahedron Letters 23(46): 4759-4762. <http://hdl.handle.net/2027.42/24161> | en_US |
dc.identifier.uri | http://www.sciencedirect.com/science/article/B6THS-42HPHH0-YB/2/be5fc07713a0a034e109cdd303c3f072 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/24161 | |
dc.description.abstract | The synthesis of 2,4-dimethoxypyrrolo[3,2-]pyrimidine () is described. This facile, 3-step synthesis involves the bromination of 2,4-dimethoxy-6-methyl-5-nitropyrimidine (), and the subsequent conversion of compound into compound . | en_US |
dc.format.extent | 160888 bytes | |
dc.format.extent | 3118 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.language.iso | en_US | |
dc.publisher | Elsevier | en_US |
dc.title | A novel method for the synthesis of 6,7-unsubstituted pyrrolo[3,2-]pyrimidines | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Materials Science and Engineering | en_US |
dc.subject.hlbsecondlevel | Chemistry | en_US |
dc.subject.hlbsecondlevel | Chemical Engineering | en_US |
dc.subject.hlbsecondlevel | Biological Chemistry | en_US |
dc.subject.hlbtoplevel | Engineering | en_US |
dc.subject.hlbtoplevel | Science | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Medicinal Chemistry College of Pharmacy and Department of Chemistry University of Michigan, Ann Arbor, Michigan 48109 U.S.A. | en_US |
dc.contributor.affiliationum | Department of Medicinal Chemistry College of Pharmacy and Department of Chemistry University of Michigan, Ann Arbor, Michigan 48109 U.S.A. | en_US |
dc.contributor.affiliationum | Department of Medicinal Chemistry College of Pharmacy and Department of Chemistry University of Michigan, Ann Arbor, Michigan 48109 U.S.A. | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/24161/1/0000419.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1016/S0040-4039(00)85706-8 | en_US |
dc.identifier.source | Tetrahedron Letters | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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