Multivalent Recognition of Flavin Derivatives Using Polymer Scaffolds

Joseph B. Carroll; Mark Gray; Kevin M. Bardon; Hiroshi Nakade; Vincent M. Rotello

doi:10.2174/1570178043400974

ISSN: 1570-1786
E-ISSN: 1875-6255

Multivalent Recognition of Flavin Derivatives Using Polymer Scaffolds
Authors: Joseph B. Carroll¹, Mark Gray², Kevin M. Bardon³, Hiroshi Nakade⁴ and Vincent M. Rotello⁵
View Affiliations Hide Affiliations

¹ Department of Chemistry, University of Massachusetts-Amherst, Amherst, Massachusetts 01003, USA ² Department of Chemistry, University of Massachusetts-Amherst, Amherst, Massachusetts 01003, USA ³ Department of Chemistry, University of Massachusetts-Amherst, Amherst, Massachusetts 01003, USA ⁴ Department of Chemistry, University of Massachusetts-Amherst, Amherst, Massachusetts 01003, USA ⁵ Department of Chemistry, University of Massachusetts-Amherst, Amherst, Massachusetts 01003, USA
Source: Letters in Organic Chemistry, Volume 1, Issue 3, Jul 2004, p. 227 - 230
DOI: https://doi.org/10.2174/1570178043400974
- Available online: 01 Jul 2004

Abstract

Random copolymers of polystyrene were functionalized with diamidopyridine and anthracene recognition elements. Cooperative recognition between isobutyl flavin “guest” molecules and mixed recognition unit modified “host” copolymers was observed arising from a combination of aromatic stacking and hydrogen bonding interactions.

Article metrics loading...

/content/journals/loc/10.2174/1570178043400974

2004-07-01

2025-06-18

From This Site

/content/journals/loc/10.2174/1570178043400974

dcterms_title,dcterms_subject,pub_keyword

-contentType:Contributor -contentType:Concept -contentType:Institution

10

5

Full text loading...

/content/journals/loc/10.2174/1570178043400974

Article Type: Review Article

Keyword(s): cooperative non-covalent interactions; hydrogen bonding; stacking; supramolecular polymers

Multivalent Recognition of Flavin Derivatives Using Polymer Scaffolds

Abstract

From This Site

Most Read This Month

Most Cited Most Cited RSS feed

Vilsmeier-Haack Cyclisation as a Facile Synthetic Route to Thieno [2,3- b] Quinolines (Part I)

Efficient Synthesis of 4-Arylmethylene-3-methylisoxazol-5(4H)-one Derivatives Catalyzed by Malic Acid

Wonderful Natural Drugs with Surprising Nutritional Values, Rheum Species, Gifts of the Nature

Novel Derivatives Based on Zerumbone Scaffold as Potential Anticancer Inhibitors

A Review on the Syntheses and Applications of the 5H-chromeno[2,3- b]pyridines

Fe Doped Ga2O3 Nanomaterial Catalysed Green and Efficient One Pot Three Component Synthesis of Tetrahydrobenzo[b]pyran

Sulfonated Ethylenediamine Functionalized Magnetic Nanoparticles as a Highly Efficient Heterogeneous Nanocatalyst for the Green Synthesis of 2,3-Dihydroquinazolin-4(1H)-ones

K2CO3/TBAB, a Composite of Inorganic and Organic Salts, a Novel and Powerful Media for Regioselective Michael Addition of Dihydropyrimidinones to Acrylic Esters Under and Without Solvent Conditions

Decomposition Kinetics of 1,1-Dihydroperoxycyclohexane in Some Organic Solvents

In Silico Screening of Some Anti-Cancer Drugs Against the Main Protease of COVID-19 Using Molecular Docking