Literature DB >> 24113332

A tetrazine templated method for the synthesis of ternary conjugates.

Boddu Venkateswara Rao1, Snehal Dhokale, Pattuparambil R Rajamohanan, Srinivas Hotha.   

Abstract

Conjugation is an important reaction that enables coupling of molecules. Many protocols exist for the synthesis of binary conjugates from two different molecules or for the polyvalent display of a single molecule. There aren't many methods for the synthesis of ternary conjugates. However, methods for ternary conjugation are important for understanding the interplay of interactions between three biomolecules (or any three molecules per se). A strategy for ternary bioconjugation using inverse electron demand Diels-Alder reaction with tetrazine is studied. Ternary conjugation was demonstrated by the reaction of a model glyco-peptide binary conjugate with a fluorescent tagged olefin.

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Year:  2013        PMID: 24113332     DOI: 10.1039/c3cc46634e

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


  3 in total

1.  Chemical Approach to Positional Isomers of Glucose-Platinum Conjugates Reveals Specific Cancer Targeting through Glucose-Transporter-Mediated Uptake in Vitro and in Vivo.

Authors:  Malay Patra; Samuel G Awuah; Stephen J Lippard
Journal:  J Am Chem Soc       Date:  2016-09-16       Impact factor: 15.419

2.  Kinetic studies of inverse electron demand Diels-Alder reactions (iEDDA) of norbornenes and 3,6-dipyridin-2-yl-1,2,4,5-tetrazine.

Authors:  Astrid-Caroline Knall; Manuel Hollauf; Christian Slugovc
Journal:  Tetrahedron Lett       Date:  2014-08-20       Impact factor: 2.415

3.  Synthesis of novel conjugates of a saccharide, amino acids, nucleobase and the evaluation of their cell compatibility.

Authors:  Dan Yuan; Xuewen Du; Junfeng Shi; Ning Zhou; Abdulgader Ahmed Baoum; Bing Xu
Journal:  Beilstein J Org Chem       Date:  2014-10-16       Impact factor: 2.883

  3 in total

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