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Henning W. M. Priepke

University of Cambridge

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Featured researches published by Henning W. M. Priepke.

Tetrahedron Letters | 1994

Dispiroketals in synthesis (part 7): Protection of D-glucopyranose substrates

Andrew B. Hughes; Steven V. Ley; Henning W. M. Priepke; Martin Woods

Abstract The formation of 1,8,13,16-tetraoxadispiro[5.0.5.4]hexadecanes (dispiroketals) of various D-glucopyranosyl substrates is described.

Journal of The Chemical Society-perkin Transactions 1 | 1997

Preparation, structure, derivatisation and NMR data ofcyclohexane-1,2-diacetal protected carbohydrates

Peter Grice; Steven V. Ley; Jörg Pietruszka; Henning W. M. Priepke; Stuart L. Warriner

Acid catalysed reaction of monosaccharides with 1,1,2,2-tetramethoxycyclohexane results in selective protection of vicinal, diequatorial, diol functionality as a cyclohexane-1,2-diacetal (CDA). This new methodology complements classical cyclic acetal protecting group strategies which in general are not able to mask diols with such diequatorial stereochemistry. The resulting CDA protected derivatives can be readily functionalised to give rapid access to numerous key building blocks for oligosaccharide and natural product synthesis.

Chemical Reviews | 2001

1,2-Diacetals: A new opportunity for organic synthesis

Steven V. Ley; Daniel K. Baeschlin; Darren J. Dixon; Alison C. Foster; Stuart J. Ince; Henning W. M. Priepke; Dominic J. Reynolds

Angewandte Chemie | 1994

A Facile One-Pot Synthesis of a Trisaccharide Unit from the Common Polysaccharide Antigen of Group B Streptococci Using Cyclohexane-1, 2-diacetal (CDA) Protected Rhamnosides†

Steven V. Ley; Henning W. M. Priepke

Angewandte Chemie | 1994

Cyclohexane‐1,2‐diacetals (CDA): A New Protecting Group for Vicinal Diols in Carbohydrates

Steven V. Ley; Henning W. M. Priepke; Stuart L. Warrine

Chemistry: A European Journal | 2006

A New Strategy for Oligosaccharide Assembly Exploiting Cyclohexane‐1,2‐diacetal Methodology: An Efficient Synthesis of a High Mannose Type Nonasaccharide

Peter Grice; Steven V. Ley; Jörg Pietruszka; Helen M. I. Osborn; Henning W. M. Priepke; Stuart L. Warriner

Angewandte Chemie | 1996

Synthesis of the Nonamannan Residue of a Glycoprotein with High Mannose Content

Peter Grice; Steven V. Ley; Jörg Pietruszka; Henning W. M. Priepke

Angewandte Chemie | 1994

Eintopfsynthese einer Trisaccharideinheit des gemeinen Polysaccharid‐Antigens von Streptococci der Gruppe B unter Verwendung Cyclohexan‐1,2‐diacetal(CDA)‐geschützter Rhamnoside

Steven V. Ley; Henning W. M. Priepke

Synlett | 1995

Tuning the Reactivity of Glycosides: Efficient One-pot Oligosaccharide Synthesis1

Peter Grice; Steven V. Ley; Jörg Pietruszka; Henning W. M. Priepke; Eric Walther

Chemische Berichte | 1990

Asymmetric Induction in the Wittig-Still Rearrangement of Ethers Containing an Allylic Stereocenter – Diastereocontrol by Allylic Nitrogen

Henning W. M. Priepke; Reinhard Brückner

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Steven V. Ley

University of Cambridge

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Stuart L. Warriner

University of Leeds

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Peter Grice

University of Cambridge

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Jörg Pietruszka

Forschungszentrum Jülich

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Reinhard Brückner

University of Freiburg

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Helen M. I. Osborn

University of Reading

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Andrew B. Hughes

University of Cambridge

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Martin Woods

Imperial College London

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Alison C. Foster

University of Oxford

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Daniel K. Baeschlin

University of Cambridge

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