Stereoselective synthesis of (E)-4-alkylidenecyclopent-2-en-1-ones by a tandem ring closure−michael addition−elimination

Ballini, Roberto; Bosica, Giovanna; Fiorini, Dennis; Gil, Maria Victoria; Petrini, Marino

Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/24669

Full metadata record

DC Field	Value	Language
dc.contributor.author	Ballini, Roberto	-
dc.contributor.author	Bosica, Giovanna	-
dc.contributor.author	Fiorini, Dennis	-
dc.contributor.author	Gil, Maria Victoria	-
dc.contributor.author	Petrini, Marino	-
dc.date.accessioned	2017-12-14T10:06:13Z	-
dc.date.available	2017-12-14T10:06:13Z	-
dc.date.issued	2001	-
dc.identifier.citation	Ballini, R., Bosica, G., Fiorini, D., Gil, M. V., & Petrini, M. (2001). Stereoselective synthesis of (E)-4-alkylidenecyclopent-2-en-1-ones by a tandem ring closure−michael addition−elimination. Organic Letters, 3(9), 1265-1267.	en_GB
dc.identifier.uri	https://www.um.edu.mt/library/oar//handle/123456789/24669	-
dc.description.abstract	Reaction of (Z)-1,4-diketones with various functionalized nitroalkanes in the presence of DBU gives 4-alkylidenecyclopent-2-en-1-ones with E selectivity. A cyclopentadienone intermediate is probably formed by intramolecular aldol condensation, and this reacts with a nitroalkane giving a Michael addition−elimination.	en_GB
dc.language.iso	en	en_GB
dc.publisher	American Chemical Society	en_GB
dc.rights	info:eu-repo/semantics/restrictedAccess	en_GB
dc.subject	Asymmetric synthesis	en_GB
dc.subject	Chemistry, Analytic	en_GB
dc.title	Stereoselective synthesis of (E)-4-alkylidenecyclopent-2-en-1-ones by a tandem ring closure−michael addition−elimination	en_GB
dc.type	article	en_GB
dc.rights.holder	The copyright of this work belongs to the author(s)/publisher. The rights of this work are as defined by the appropriate Copyright Legislation or as modified by any successive legislation. Users may access this work and can make use of the information contained in accordance with the Copyright Legislation provided that the author must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the prior permission of the copyright holder.	en_GB
dc.description.reviewed	peer-reviewed	en_GB
dc.identifier.doi	10.1021/ol0069352	-
dc.publication.title	Organic Letters	en_GB
Appears in Collections:	Scholarly Works - FacSciChe

Files in This Item:

File	Description	Size	Format
ballini2001 (4).pdf Restricted Access		35.38 kB	Adobe PDF	View/Open Request a copy

Show simple item record Statistics