Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/19225
Share/Export:
logo share SHARE logo core CORE BASE
Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE
Title

3-(Aminomethyl)-2-(carboxymethyl)isoxazolidinyl nucleosides: building blocks for peptide nucleic acid analogues

AuthorsMerino, Pedro CSIC ORCID ; Tejero, Tomás CSIC ORCID; Matés, Juan; Chiacchio, Ugo; Corsaro, Antonio; Romeo, Giovanni
Issue Date17-Jun-2007
PublisherElsevier
CitationTetrahedron Asymmetry 18(13): 1517-1520 (2007)
AbstractThe synthesis of orthogonally protected 3-(aminomethyl)-2-(carboxymethyl)isoxazolidinyl thymine, a convenient monomer for the preparation of novel isoxazolidinyl peptide nucleic acid analogues, has been achieved through enantioselective 1,3-dipolar cycloaddition between N-glycosyl nitrones and vinyl acetate.
Description4 pages, 3 schemes, 1 table, 1 chart.
Publisher version (URL)http://dx.doi.org/10.1016/j.tetasy.2007.06.029
URIhttp://hdl.handle.net/10261/19225
DOI10.1016/j.tetasy.2007.06.029
ISSN0957-4166
Appears in Collections:(ICMA) Artículos

Show full item record
Review this work

SCOPUSTM   
Citations

17
checked on Jan 1, 2022

WEB OF SCIENCETM
Citations

13
checked on Jan 16, 2022

Page view(s)

297
checked on Jan 16, 2022

Google ScholarTM

Check

Altmetric

Dimensions


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