Hydroxy-Functionalized Dendritic Building Blocks

A convenient and practical multi‐gram procedure for the synthesis of second‐ (G2; 4a, 5a, 5d) and third‐generation (G3; 6a) dendrons with orthogonally protected functional groups in the periphery (hydroxy) and at the focal point (carboxylic acid) is described. It uses the amply available first‐gener...

Full description

Saved in:
Bibliographic Details
Published inEuropean journal of organic chemistry Vol. 1998; no. 11; pp. 2551 - 2556
Main Authors Ingerl, Andrea, Neubert, Ingo, Klopsch, Rainer, Schlüter, A. Dieter
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag GmbH 01.11.1998
WILEY‐VCH Verlag GmbH
Wiley
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:A convenient and practical multi‐gram procedure for the synthesis of second‐ (G2; 4a, 5a, 5d) and third‐generation (G3; 6a) dendrons with orthogonally protected functional groups in the periphery (hydroxy) and at the focal point (carboxylic acid) is described. It uses the amply available first‐generation dendrons with amine and carboxylic ester functions (1) and tetrahydropyranyl‐protected hydroxy and carboxylic acid functions (2b, 3), respectively, which are connected via amides by peptide methods. Purification is either done by recrystallization or simple filtration through silica gel and yields the products as analytically pure materials on a several‐gram scale (even for G3). ‘The dendrons’ protective groups are proven to be orthogonal (500‐MHz NMR) which makes them useful components (building blocks) of a future dendron construction kit for a versatile synthesis of, for example, dendronized polymers.
Bibliography:istex:ACCD9A6B97DCA2AD675BF7D717E77B6730B32E3E
ArticleID:EJOC2551
ark:/67375/WNG-1Z51XQFW-1
ISSN:1434-193X
1099-0690
DOI:10.1002/(SICI)1099-0690(199811)1998:11<2551::AID-EJOC2551>3.0.CO;2-Y