Literature DB >> 11893173

Solution-phase synthesis of aminooxy peptoids in the C to N and N to C directions.

Injae Shin1, Kisoo Park.   

Abstract

[structure: see text] Aminooxy peptoids, which are potential peptidomimetics, were synthesized by a stepwise monomer assembly. Ns-protected N-substituted aminooxyacetate tert-butyl esters were used as a monomer in both the C to N and the N to C directions. Submonomer synthesis of aminooxy peptoids is also described.

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Year:  2002        PMID： 11893173     DOI： 10.1021/ol010251s

Source DB:  PubMed          Journal:  Org Lett        ISSN： 1523-7052            Impact factor:   6.005


  4 in total

1.  Hydrazone- and hydrazide-containing N-substituted glycines as peptoid surrogates for expedited library synthesis: application to the preparation of Tsg101-directed HIV-1 budding antagonists.

Authors:  Fa Liu; Andrew G Stephen; Catherine S Adamson; Karine Gousset; M Javad Aman; Eric O Freed; Robert J Fisher; Terrence R Burke
Journal:  Org Lett       Date:  2006-10-26       Impact factor: 6.005

2.  Synthesis and Application of Methyl N,O-Hydroxylamine Muramyl Peptides.

Authors:  Klare M Lazor; Junhui Zhou; Kristen E DeMeester; Elizabeth A D'Ambrosio; Catherine L Grimes
Journal:  Chembiochem       Date:  2019-03-21       Impact factor: 3.164

3.  Catalysis-based enantioselective total synthesis of the macrocyclic spermidine alkaloid isooncinotine.

Authors:  Bodo Scheiper; Frank Glorius; Andreas Leitner; Alois Fürstner
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-12       Impact factor: 11.205

Review 4.  Solid-phase synthesis of N-substituted glycine oligomers (alpha-peptoids) and derivatives.

Authors:  Adrian S Culf; Rodney J Ouellette
Journal:  Molecules       Date:  2010-08-04       Impact factor: 4.411
  4 in total

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