English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/52165
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
Exportar a otros formatos:


Access to the cis-fused stereoisomers of proline analogues containing an octahydroindole core

AuthorsSayago, Francisco J. ; Laborda, Pedro ; Calaza, M. Isabel ; Jiménez, Ana I. ; Cativiela, Carlos
Issue Date2011
CitationEuropean Journal of Organic Chemistry 11: 2011-2028 (2011)
AbstractAn overview of the synthetic methods developed to build all the cis-fused stereoisomers of octahydroindole-2-carboxylic acid and its α-methylated derivative in enantiomerically pure form is presented. Both asymmetric synthetic strategies(auxiliary- or substrate-controlled processes) and procedures based on the resolution of racemic compounds (chemical, enzymatic, and chromatographic processes) are summarized. Special emphasis has been placed on those strategies able to provide multigram quantities of enantiopure compounds, a prerequisite to make downstream biological applications feasible.
DescriptionEl pdf del artículo es la versión post-print.
Publisher version (URL)http://dx.doi.org/10.1002/ejoc.201001710
Identifiersdoi: 10.1002/ejoc.201001710
issn: 1434-193X
e-issn: 1099-0690
Appears in Collections:(ICMA) Artículos
Files in This Item:
File Description SizeFormat 
Access to the cis-Fused.pdf468,62 kBAdobe PDFThumbnail
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.