Optical rotatory dispersion and absolute configuration--V. : The absolute configuration of natural plasmalogen
dc.contributor.author | Craig, J. Cymerman | en_US |
dc.contributor.author | Hamon, D. P. G. | en_US |
dc.contributor.author | Purushothaman, K. K. | en_US |
dc.contributor.author | Roy, S. K. | en_US |
dc.contributor.author | Lands, William E. M. | en_US |
dc.date.accessioned | 2006-04-17T16:18:47Z | |
dc.date.available | 2006-04-17T16:18:47Z | |
dc.date.issued | 1966 | en_US |
dc.identifier.citation | Craig, J. Cymerman, Hamon, D. P. G., Purushothaman, K. K., Roy, S. K., Lands, W. E. M. (1966)."Optical rotatory dispersion and absolute configuration--V. : The absolute configuration of natural plasmalogen." Tetrahedron 22(1): 175-178. <http://hdl.handle.net/2027.42/33498> | en_US |
dc.identifier.uri | http://www.sciencedirect.com/science/article/B6THR-42M85CJ-72/2/fc10563c46f8aadc0fa495eaecd08f9d | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/33498 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=5927157&dopt=citation | en_US |
dc.description.abstract | The 1-alkenylglycerol (III) and 1-alkylglycerol (II) obtained from natural plasmalogen (I) have been shown by optical rotatory dispersion measurements to have the same absolute configuration as natural chimyl and batyl alcohol. All compounds are -l-glycerol ethers. | en_US |
dc.format.extent | 279581 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 | Optical rotatory dispersion and absolute configuration--V. : The absolute configuration of natural plasmalogen | 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 Biological Chemistry, University of Michigan, Ann Arbor, Michigan U.S.A. | en_US |
dc.contributor.affiliationother | Department of Pharmaceutical Chemistry, University of California, San Francisco, California 94122 U.S.A. | en_US |
dc.contributor.affiliationother | Department of Pharmaceutical Chemistry, University of California, San Francisco, California 94122 U.S.A. | en_US |
dc.contributor.affiliationother | Department of Pharmaceutical Chemistry, University of California, San Francisco, California 94122 U.S.A. | en_US |
dc.contributor.affiliationother | Department of Pharmaceutical Chemistry, University of California, San Francisco, California 94122 U.S.A. | en_US |
dc.identifier.pmid | 5927157 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/33498/1/0000904.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1016/0040-4020(66)80115-1 | en_US |
dc.identifier.source | Tetrahedron | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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