English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/19413
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE
Exportar a otros formatos:


Efficient synthesis of a new pipecolic acid analogue with a bicyclic structure

AuthorsCasabona, Diego; Cativiela, Carlos
KeywordsConstrained amino acid
Quaternary amino acid
Proline analogue
2,5-Ethanepipecolic acid
Chemoselective reduction
Issue Date16-Oct-2006
CitationTetrahedron 62(42): 10000-10004 (2006)
AbstractThis report describes the synthesis of 2-azabicyclo[2.2.2]octane-1-carboxylic acid, a constrained pipecolic acid analogue. The route gives a very good total yield starting from cheap and readily available compounds and uses very easy reactions.
Description5 pages, 3 figures, scheme 1.
Publisher version (URL)http://dx.doi.org/10.1016/j.tet.2006.08.006
Appears in Collections:(ICMA) Artículos
Files in This Item:
There are no files associated with this item.
Show full item record
Review this work

Related articles:

WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.