Allene Synthesis from 2-Alkyn-1-Ols

DSpace/Manakin Repository

dc.contributor.author	Kuo, Elaine Y.
dc.contributor.author	Finney, Nathaniel S.
dc.contributor.author	Myers, Andrew
dc.date.accessioned	2009-06-26T17:08:54Z
dc.date.issued	1989
dc.identifier.citation	Myers, 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.issn	0040-4039	en
dc.identifier.uri	http://nrs.harvard.edu/urn-3:HUL.InstRepos:3122543
dc.description.abstract	Activation 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.sponsorship	Chemistry and Chemical Biology	en
dc.language.iso	en_US	en
dc.publisher	Elsevier	en
dc.relation.isversionof	http://dx.doi.org/10.1016/S0040-4039(00)76187-9	en
dc.relation.hasversion	http://www.chem.harvard.edu/groups/myers/pdf_publications/tetlet_1989_30_5747.pdf	en
dash.license	META_ONLY
dc.title	Allene Synthesis from 2-Alkyn-1-Ols	en
dc.type	Journal Article
dc.description.version	Version of Record
dc.relation.journal	Tetrahedron Letters	en
dash.depositing.author	Myers, Andrew
dash.embargo.until	10000-01-01