Part I, Tetrasubstituted allenyl ethers: Part Ii, Triply convergent cyclopentannelation

dc.contributor.author	Tokeshi, Bradley K.
dc.date.accessioned	2011-07-21T23:04:40Z
dc.date.available	2011-07-21T23:04:40Z
dc.date.issued	2006
dc.description.abstract	Part I: A method for the synthesis of tetrasubstituted allene ethers is described. The Brook rearrangement is employed to form key propargyl ether intermediates. The resulting propargyl ethers are isomerized to allenes. The allenes are used in the cyclopentannelation reaction to form β, β-disubstituted cyclopentenones. Part II: Based on methodology developed by our group, the scope of the triply convergent cyc1openmnnelation is expanded. Modifications to the existing protocol are described. An expanded set of morpholino enamides are employed.
dc.description.degree	M.S.
dc.identifier.uri	http://hdl.handle.net/10125/20468
dc.language	eng
dc.publisher	University of Hawaii at Manoa
dc.relation	Theses for the degree of Master of Science (University of Hawaii at Manoa). Chemistry; no. 4107
dc.rights	All UHM dissertations and theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission from the copyright owner.
dc.subject	Ethers
dc.title	Part I, Tetrasubstituted allenyl ethers: Part Ii, Triply convergent cyclopentannelation
dc.type	Thesis
dc.type.dcmi	Text

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