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dc.contributor.authorMyers, Andrew
dc.contributor.authorFinney, Nathaniel S.
dc.contributor.authorKuo, Elaine Y.
dc.date.accessioned2009-06-26T17:08:54Z
dc.date.issued1989
dc.identifier.citationMyers, Andrew G., Nathaniel S. Finney, and Elaine Y. Kuo. 1989. Allene synthesis from 2-alkyn-1-Ols. Tetrahedron Letters 30(42): 5747-5750.en
dc.identifier.issn0040-4039en
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:3122543
dc.description.abstractActivation of 2-alkyn-1-01s as their methanesulfonate esters and displacement with hydrazine urnishes the corresponding alkynyl hydrazine derivatives which undergo smooth oxidative rearrangement with diethyl azodicarboxylate (DEAD) or 4-methyl-1,2,4-triazoline-3,5-dione (MTAD) to form allenes.en
dc.description.sponsorshipChemistry and Chemical Biologyen
dc.language.isoen_USen
dc.publisherElsevieren
dc.relation.isversionofhttp://dx.doi.org/10.1016/S0040-4039(00)76187-9en
dc.relation.hasversionhttp://www.chem.harvard.edu/groups/myers/pdf_publications/tetlet_1989_30_5747.pdfen
dash.licenseMETA_ONLY
dc.titleAllene Synthesis from 2-Alkyn-1-Olsen
dc.typeJournal Article
dc.description.versionVersion of Record
dc.relation.journalTetrahedron Lettersen
dash.depositing.authorMyers, Andrew
dash.embargo.until10000-01-01
dc.identifier.doi10.1016/S0040-4039(00)76187-9*
dash.contributor.affiliatedMyers, Andrew


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