Sequential [3+2] and [4+2] Cycloadditions for Stereoselective Synthesis of a Novel Polyheterocyclic Scaffold

doi:10.1021/co400026s

完整後設資料紀錄

DC 欄位	值	語言
dc.contributor.author	Lu, Qing	en_US
dc.contributor.author	Xin Huang	en_US
dc.contributor.author	Song, Gonghua	en_US
dc.contributor.author	Sun, Chung-Ming	en_US
dc.contributor.author	Jasinski, Jerry P.	en_US
dc.contributor.author	Keeley, Amanda C.	en_US
dc.contributor.author	Zhang, Wei	en_US
dc.date.accessioned	2014-12-08T15:31:12Z	-
dc.date.available	2014-12-08T15:31:12Z	-
dc.date.issued	2013-07-01	en_US
dc.identifier.issn	2156-8952	en_US
dc.identifier.uri	http://dx.doi.org/10.1021/co400026s	en_US
dc.identifier.uri	http://hdl.handle.net/11536/22221	-
dc.description.abstract	A strategy of combining [3 + 2] cycloaddition and intramolecular Diels-Alder reaction is developed for the [3 + 2] cycloaddition of azomethine ylides and maleimides were derivatized for intramolecular Diels-Alder reaction of furan to form highly condensed heterocyclic products as racemic single diastereomers.	en_US
dc.language.iso	en_US	en_US
dc.subject	sequential cycloadditions	en_US
dc.subject	stereoselective annulation	en_US
dc.subject	[3+2] cycloaddition	en_US
dc.subject	intramolecular Diels-Alder reaction	en_US
dc.subject	polyheterocyclic scaffold	en_US
dc.title	Sequential [3+2] and [4+2] Cycloadditions for Stereoselective Synthesis of a Novel Polyheterocyclic Scaffold	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1021/co400026s	en_US
dc.identifier.journal	ACS COMBINATORIAL SCIENCE	en_US
dc.citation.volume	15	en_US
dc.citation.issue	7	en_US
dc.citation.spage	350	en_US
dc.citation.epage	355	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:000321793500005	-
dc.citation.woscount	0	-
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