Show simple item record

A Convenient Synthesis of 2‐ N ‐Methoxycarbonylaminooxazolo[5,4‐ d ]pyrimidines

dc.contributor.authorChern, Ji‐wangen_US
dc.contributor.authorWise, Dean S.en_US
dc.contributor.authorTownsend, Leroy B.en_US
dc.date.accessioned2013-02-12T19:00:31Z
dc.date.available2013-02-12T19:00:31Z
dc.date.issued1984-07en_US
dc.identifier.citationChern, Ji‐wang ; Wise, Dean S.; Townsend, Leroy B. (1984). "A Convenient Synthesis of 2â N â Methoxycarbonylaminooxazolo[5,4â d ]pyrimidines ." Journal of Heterocyclic Chemistry 21(4): 1245-1246. <http://hdl.handle.net/2027.42/96274>en_US
dc.identifier.issn0022-152Xen_US
dc.identifier.issn1943-5193en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/96274
dc.description.abstractA facile synthesis of methyl oxazolo[5,4‐ d ]pyrimidine‐2‐carbamic acids by the cyclodesulfurization of a methoxycarbonyl thiourea with dicyclohexylcarbodiimide is described.en_US
dc.publisherWiley‐Blackwellen_US
dc.titleA Convenient Synthesis of 2‐ N ‐Methoxycarbonylaminooxazolo[5,4‐ d ]pyrimidinesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelOrganic Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Medicinal Chemistry, College of Pharmacy and Department of Chemistry, University of Michigan, Ann Arbor, Michigan, 48109–1065en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/96274/1/5570210467_ftp.pdf
dc.identifier.doi10.1002/jhet.5570210467en_US
dc.identifier.sourceJournal of Heterocyclic Chemistryen_US
dc.identifier.citedreferenceY. Ohtsuka, Chem. Pharm. Bull., 18, 2242 ( 1970 ).en_US
dc.identifier.citedreferenceY. Ohtsuka, Bull. Chem. Soc. Japan, 43, 954 ( 1970 ).en_US
dc.identifier.citedreferenceV. D. Patil and L. B. Townsend, J. Heterocyclic Chem., 8, 503 ( 1971 ).en_US
dc.identifier.citedreferenceR. Esmail and F. Kurger, Synthesis, 301 ( 1975 ).en_US
dc.identifier.citedreferenceB. George and E. P. Papadopoulos, J. Heterocyclic Chem., 20, 1127 ( 1983 ).en_US
dc.identifier.citedreferenceR. W. Lamon, J. Heterocyclic Chem., 5, 837 ( 1968 ).en_US
dc.identifier.citedreferenceT. Matsiu, M. Nagano, J. Tobitsuka and K. Oyamasla, Yakugaku Zasshi, 93, 977 ( 1973 ); Chem. Abstr., 79, 105139m ( 1973 ).en_US
dc.identifier.citedreferenceC. C. Beard,U. S. Patent, 4,191,764( 1980 ).en_US
dc.identifier.citedreferenceC. W. Noell and R. K. Robins, J. Med. Chem., 5, 558 ( 1962 ).en_US
dc.identifier.citedreferenceW. Pfleiderer, R. Mengel and P. Hemmerich, Chem. Ber., 104, 2273 ( 1971 ).en_US
dc.identifier.citedreferenceaMethoxycarbonyl isothiocyanate was prepared by adding methyl chloroformate dropwise to a suspension of potassium isothiocyanate in acetonitrile A. E. Dixon and J. Taylor, J. Chem. Soc., 93, 684 ( 1908 ); b R. W. Lamon, J. Heterocyclic Chem., 5, 837 ( 1968 ).en_US
dc.identifier.citedreferenceJ. Brown, J. App. Chem. (London), 7, 109 ( 1957 ).en_US
dc.identifier.citedreferenceA. M. M. E. Omar, N. S. Habib and O. M. Aboulwafa, Synthesis, 864 ( 1977 ).en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.