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 |
|