High pressure chiral recognition experiments - A route to homochiral 4-fluorocyclohexenones

Meibom, Daniel; Weinmann, Hilmar; Winterfeldt, Ekkehard

dc.identifier.uri	http://dx.doi.org/10.15488/1921
dc.identifier.uri	http://www.repo.uni-hannover.de/handle/123456789/1946
dc.contributor.author	Meibom, Daniel
dc.contributor.author	Weinmann, Hilmar
dc.contributor.author	Winterfeldt, Ekkehard
dc.date.accessioned	2017-09-14T14:08:58Z
dc.date.available	2017-09-14T14:08:58Z
dc.date.issued	2004
dc.identifier.citation	Meibom, D.; Weinmann, H.; Winterfeldt, E.: High pressure chiral recognition experiments - A route to homochiral 4-fluorocyclohexenones. In: Arkivoc 2004 (2004), Nr. 2, S. 4-23
dc.description.abstract	4-Fluorocyclohexadienones, prepared by an improved Jacquesy-process, were shown to undergo highly face-selective Diels-Alder reactions with the homochiral cyclopentadiene 1. Some of the diastereoselective transformations, quite unique rearrangements of ?-hydroxy compounds resulting from nucleophilic attack to the carbonyl group as well as selected Retro-Diels-Alder reactions, are reported.	eng
dc.description.sponsorship	DFG
dc.description.sponsorship	Fonds der Chemischen Industrie
dc.language.iso	eng
dc.publisher	Gainesville : Arkat USA
dc.relation.ispartofseries	Arkivoc 2004 (2004), Nr. 2
dc.rights	CC BY-NC 3.0 Unported
dc.rights.uri	https://creativecommons.org/licenses/by-nc/3.0
dc.subject	Asymmetric synthesis	eng
dc.subject	Chiral recognition	eng
dc.subject	Cycloadditions	eng
dc.subject	Fluorocompounds	eng
dc.subject	High pressure chemistry	eng
dc.subject.ddc	540 \| Chemie	ger
dc.title	High pressure chiral recognition experiments - A route to homochiral 4-fluorocyclohexenones	eng
dc.type	Article
dc.type	Text
dc.relation.issn	15517004
dc.bibliographicCitation.issue	2
dc.bibliographicCitation.volume	2004
dc.bibliographicCitation.firstPage	4
dc.bibliographicCitation.lastPage	23
dc.description.version	publishedVersion
tib.accessRights	frei zug�nglich