Literature DB >> 24416763

Efficient and accelerated growth of multifunctional dendrimers using orthogonal thiol-ene and SN2 reactions.

Naresh Kottari1, Yoann M Chabre, Tze Chieh Shiao, Rabindra Rej, René Roy.   

Abstract

An orthogonal coupling strategy was developed by combining thiol-ene and SN2 reactions, which was subsequently applied to the accelerated synthesis of multifunctional dendrimers using carbohydrate building blocks. In surface plasmon resonance (SPR) studies, the β-d-galactopyranoside-coated dendrimer exhibited nM binding affinity with the bacterial LecA lectin extracted from Pseudomonas aeruginosa.

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Year:  2014        PMID: 24416763     DOI: 10.1039/c3cc46633g

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

Review 1.  Modular and orthogonal synthesis of hybrid polymers and networks.

Authors:  Shuang Liu; Kevin T Dicker; Xinqiao Jia
Journal:  Chem Commun (Camb)       Date:  2015-03-28       Impact factor: 6.222

Review 2.  Applications of Thiol-Ene Chemistry for Peptide Science.

Authors:  Mark D Nolan; Eoin M Scanlan
Journal:  Front Chem       Date:  2020-11-12       Impact factor: 5.221

3.  Orthogonal dual thiol-chloroacetyl and thiol-ene couplings for the sequential one-pot assembly of heteroglycoclusters.

Authors:  Michele Fiore; Gour Chand Daskhan; Baptiste Thomas; Olivier Renaudet
Journal:  Beilstein J Org Chem       Date:  2014-07-08       Impact factor: 2.883

  3 in total

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