MO(CO)(6)-mediated synthesis of calix[4]arenes carrying beta-hydroxy ketones or alpha,beta-unsaturated-beta-amino ketones

doi:10.1016/j.tetlet.2006.10.082

完整後設資料紀錄

DC 欄位	值	語言
dc.contributor.author	Senthilvelan, Annamalai	en_US
dc.contributor.author	Tsai, Ming-Tsung	en_US
dc.contributor.author	Chang, Kai-Chi	en_US
dc.contributor.author	Chung, Wen-Sheng	en_US
dc.date.accessioned	2014-12-08T15:15:12Z	-
dc.date.available	2014-12-08T15:15:12Z	-
dc.date.issued	2006-12-18	en_US
dc.identifier.issn	0040-4039	en_US
dc.identifier.uri	http://dx.doi.org/10.1016/j.tetlet.2006.10.082	en_US
dc.identifier.uri	http://hdl.handle.net/11536/11433	-
dc.description.abstract	MO(CO)(6)-mediated ring opening reactions of calix[4]arene isoxazolines/isoxazoles provide a new synthetic methodology for calix[4]arenes carrying bifunctional beta-hydroxy ketones or alpha,beta-unsaturated-beta-amino ketones. MO(CO)(6) is a highly selective and convenient reagent for the ring opening process of these supramolecular isoxazolines/isoxazoles. (c) 2006 Elsevier Ltd. All rights reserved.	en_US
dc.language.iso	en_US	en_US
dc.subject	calix[4]arene isoxazolines/isoxazoles	en_US
dc.subject	molybdenum hexacarbonyl	en_US
dc.subject	beta-hydroxy ketones	en_US
dc.subject	alpha,beta-unsaturated-beta-amino ketones	en_US
dc.title	MO(CO)(6)-mediated synthesis of calix[4]arenes carrying beta-hydroxy ketones or alpha,beta-unsaturated-beta-amino ketones	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1016/j.tetlet.2006.10.082	en_US
dc.identifier.journal	TETRAHEDRON LETTERS	en_US
dc.citation.volume	47	en_US
dc.citation.issue	51	en_US
dc.citation.spage	9077	en_US
dc.citation.epage	9081	en_US
dc.contributor.department	應用化學系	zh_TW
dc.contributor.department	Department of Applied Chemistry	en_US
dc.identifier.wosnumber	WOS:000242556000015	-
dc.citation.woscount	11	-
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