Skip Navigation

Corrigendum for Marchán et al., Nucl. Acids Res. 34 (3) e24.
Nucleic Acids Research 2006 34(5):1668; doi:10.1093/nar/gkl110
This Article
Right arrow Full Text Freely available
Right arrow Print PDF (33K) Freely available
Right arrow Screen PDF (34K) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Marchan, V.
Right arrow Articles by Grandas, A.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Marchan, V.
Right arrow Articles by Grandas, A.
Social Bookmarking
Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Published online 29 March 2006

© The Author 2006. Published by Oxford University Press. All rights reserved
The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and Oxford University Press are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions@oxfordjournals.org

Corrigendum

Diels-Alder cycloadditions in water for the straightforward preparation of peptide–oligonucleotide conjugates

Vicente Marchan, Samuel Ortega, Daniel Pulido, Enrique Pedroso and Anna Grandas

The first 10% of the full text of this article appears below.

The following paragraph contained an error in the original publication

Synthesis of maleimide-peptide-NH2

All the amino acids of the peptide sequence were subsequently coupled on a Rink amide p-methylbenzhydrylamine resin (44) (100 mg, loading: 69 mmol NH2/mg) following the standard procedures of solid-phase peptide synthesis . . . [Full Text of this Article]


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?