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Synthesis of Oligosaccharides on Solid Support Using Thioglycosides and Pentenyl Glycosides

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2001

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https://doi.org/10.1002/0471220442.ch5
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SEEBERGER, Peter H., ed.. Solid Support Oligosaccharide Synthesis and Combinatorial Carbohydrate Libraries. New York, USA: John Wiley & Sons, Inc., 2001, pp. 99-116. ISBN 0-471-37828-3. Available under: doi: 10.1002/0471220442.ch5

Zusammenfassung

Today, a multitude of methods for formation of glycosidic linkages is available to the synthetic organic chemist. Covered here are solid‐phase oligosaccharide syntheses relying on the use of thioglycosides and n‐pentenyl glycosides as glycosyl donors. They differ from many other glycosyl donors because they are stable under a variety of reaction conditions commonly employed in oligosaccharide synthesis but at the same time can be selectively activated when required.

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540 Chemie

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ISO 690WITTMANN, Valentin, 2001. Synthesis of Oligosaccharides on Solid Support Using Thioglycosides and Pentenyl Glycosides. In: SEEBERGER, Peter H., ed.. Solid Support Oligosaccharide Synthesis and Combinatorial Carbohydrate Libraries. New York, USA: John Wiley & Sons, Inc., 2001, pp. 99-116. ISBN 0-471-37828-3. Available under: doi: 10.1002/0471220442.ch5
BibTex
@incollection{Wittmann2001-08-10Synth-42544,
  year={2001},
  doi={10.1002/0471220442.ch5},
  title={Synthesis of Oligosaccharides on Solid Support Using Thioglycosides and Pentenyl Glycosides},
  isbn={0-471-37828-3},
  publisher={John Wiley & Sons, Inc.},
  address={New York, USA},
  booktitle={Solid Support Oligosaccharide Synthesis and Combinatorial Carbohydrate Libraries},
  pages={99--116},
  editor={Seeberger, Peter H.},
  author={Wittmann, Valentin}
}
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    <dcterms:abstract xml:lang="eng">Today, a multitude of methods for formation of glycosidic linkages is available to the synthetic organic chemist. Covered here are solid‐phase oligosaccharide syntheses relying on the use of thioglycosides and n‐pentenyl glycosides as glycosyl donors. They differ from many other glycosyl donors because they are stable under a variety of reaction conditions commonly employed in oligosaccharide synthesis but at the same time can be selectively activated when required.</dcterms:abstract>
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