The benzyl esters 1 ยฑ 3 of oligo[(R)-3-hydroxybutanoic acids] (OHB) containing 2, 16, or 32 HB units were coupled at the hydroxy terminus with arginine (by esterification with carbodiimide), with glucose (by acetalization with glucosyl trichloroacetimidate), and with 7-(dimethylamino)coumarin-4-acet
Synthesis and Enzymatic Degradation of Dendrimers from (R)-3-Hydroxybutanoic Acid and Trimesic Acid
โ Scribed by Prof. Dr. Dieter Seebach; Dr. Guido F. Herrmann; Dr. Urs D. Lengweiler; dipl.-phil. II Beat M. Bachmann; Dr. Walter Amrein
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 661 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0044-8249
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a โFull Textโ option. The original article is trackable v
## Abstract Oligomers of (__R__)โ3โhydroxybutanoate (OHB) have previously been shown to transport cations through lipid bilayers. The ionโtransport activity has been attributed to the formation of hydrophobic aggregates or pores, which have been identified by fluorescenceโmicroscopy measurements of
## on the occasion of his 60th birthday To study the stereoselectivity of enzymatic cleavage of poly(3-hydroxybutyrates) (PHB) in a well-defined system (purified depolymerase and monodisperse substrate of specific relative configuration), linear and cyclic oligomers of HB (OHBs) containing (R)-and