C-Furanosides: Synthesis and Stereochemistry

Author:   Peter Goekjian (Chemistry Department, Claude Bernard University Lyon 1, Lyon, France) ,  Arnaud Haudrechy (Institute of Molecular Chemistry, Reims (ICMR), University of Reims Champagne-Ardenne, Reims, France) ,  Boudjema Menhour (Institute of Molecular Chemistry, Reims (ICMR), University of Reims Champagne-Ardenne, Reims, France) ,  Claire Coiffier (Institute of Molecular Chemistry, Reims (ICMR), University of Reims Champagne-Ardenne, Reims, France)
Publisher:   Elsevier Science Publishing Co Inc
ISBN:  

9780128037393


Pages:   794
Publication Date:   30 November 2017
Format:   Paperback
Availability:   Manufactured on demand   Availability explained
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C-Furanosides: Synthesis and Stereochemistry


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Author:   Peter Goekjian (Chemistry Department, Claude Bernard University Lyon 1, Lyon, France) ,  Arnaud Haudrechy (Institute of Molecular Chemistry, Reims (ICMR), University of Reims Champagne-Ardenne, Reims, France) ,  Boudjema Menhour (Institute of Molecular Chemistry, Reims (ICMR), University of Reims Champagne-Ardenne, Reims, France) ,  Claire Coiffier (Institute of Molecular Chemistry, Reims (ICMR), University of Reims Champagne-Ardenne, Reims, France)
Publisher:   Elsevier Science Publishing Co Inc
Imprint:   Academic Press Inc
Weight:   1.250kg
ISBN:  

9780128037393


ISBN 10:   0128037393
Pages:   794
Publication Date:   30 November 2017
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Paperback
Publisher's Status:   Active
Availability:   Manufactured on demand   Availability explained
We will order this item for you from a manufactured on demand supplier.

Table of Contents

The Stereochemistry of C-Furanosides  Part A. C-Glycosides of Lyxose and Ribose: galacto-, altro- and allo- Configurations A. Introduction A.1. galacto-C-Furanosides (I, b-C-Lyxose) A.2. D- and  L-altro-C-furanosides (II/ent-II,  a-C-Lyxose, a-C-Ribose) A.3. allo-C-Furanosides (VI, b-C-Ribose) A.4. Lyxose and  Ribose C-Glycosides: Other Results and  Further  Insight Into  Stereochemistry Part B. C-Glycosides of Arabinose and Xylose: gluco-, ido- and manno- Configurations B. Introduction B.1. Gluco-C-Furanosides (III/ent-III,  b-C-Arabinose, b-C-Xylose) B.2. ido-C-Furanosides (V/ent-V, a-C-Xylose) B.3. manno-C-Furanosides (VII/ent-VII, a-C-Arabinose) B.4. Arabinose and  Xylose C-Furanosides: Other Results and  Further  Insight Into  Stereochemistry Part C. Applications of C-Furanosides Introduction C.1. Preparation of C-Furanosides   C.2. Agro-Industry and  Farming   C.3. Ligands for Asymmetric  Catalysis   C.4. Perfumes, Aromas,  and  Cosmetics   C.5. Imaging  and  Diagnostics C.6. Pharmaceutical Industry   C.7. Polymers Part D. 1H NMR Vicinal Coupling Constants of C-Furanosides Introduction   D.1. 1H NMR Data  in galacto-C-Furanosides (I, b-C-Lyxose), Corresponding to Chapter A.1  D.2. 1H NMR Data  in D- and  L-altro-C-Furanosides (II/ent-II, a-C-Lyxose,  a-C-Ribose), Corresponding to Chapter A.2  D.3. Comparison Between 1H NMR Data  in galacto-C-Furanosides (I, b-C-Lyxose),  Corresponding to Chapter A.1, and  in D- and  L-altro-C-Furanosides (II/ent-II,  a-C-Lyxose,  a-C-Ribose), Corresponding to Chapter A.2  D.4. 1H NMR Data  in allo-C-Furanosides (VI, b-C-Ribose), Corresponding to Chapter A.3  D.5. Comparison Between 1H NMR Data  in D- and  L-altro-C-Furanosides (II/ent-II,  a-C-Lyxose,  a-C-Ribose), Corresponding to Chapter A.2, and  in allo-C-Furanosides (VI, b-C-Ribose), Corresponding to Chapter A.3  D.6. 1H NMR Data  in D- and  L-gluco-C-Furanosides (III/ent-III,  b-C-Arabinose, b-C-Xylose),  Corresponding to Chapter B.1  D.7/ 1H NMR Data  in D- and  L-ido-C-Furanosides (V/ent-V, a-C-D-Xylose, a-C-L-Xylose),  Corresponding to Chapter B.2  D.8. Comparison Between 1H NMR Data  in D- and  L-gluco- C-Furanosides (III/ent-III,  b-C-Arabinose, b-C-Xylose), Corresponding to Chapter B.1, and  in D- and  L-ido-C-Furanosides (V/ent-V, a-C-D-Xylose, a-C-L-Xylose), Corresponding to Chapter B.2  D.9. 1H NMR Data  in D- and  L-manno-C-Furanosides(VII/ent-VII, a-C-Arabinose), Corresponding to Chapter B.3  D.10. Comparison Between 1H NMR Data  in galacto-C-Furanosides (I, b-C-Lyxose),  Corresponding to Chapter A.1, and  in D- and  L-gluco-C-Furanosides (III/ent-III, b-C-Arabinose, b-C-Xylose),  Corresponding to Chapter B.1  D.11  Comparison Between 1H NMR Data  in D- and  L-altro- C-Furanosides (II/ent-II,  a-C-Lyxose, a-C-Ribose), Corresponding to Chapter A.2, and  in D- and  L-ido- C-Furanosides (V/ent-V, a-C-D-Xylose, a-C-L-Xylose), Corresponding to Chapter B.2  D.12. Conclusion and  Summary  of Expected Coupling Constants  

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Dr. Peter Goekjian has been Professor of Chemistry at Université Claude Bernard–Lyon 1, France, since September 2000. His research interests are carbohydrate chemistry, total synthesis of glycosidic natural products, targeted methodology, and the role of glycosylation in signal transduction and gene expression. He was involved in the early work on the use of C-glycosides as conformational probes in the late 1980s and early 1990s. Dr. Arnaud Haudrechy has been a Professor of Chemistry at the Université of Reims Champagne Ardenne, France, since September 2003. His research interests include carbohydrate chemistry, total synthesis of natural substances, development of methodologies, and didactical techniques. He was involved in the early work on the use of C-glycosides as conformational probes in the late 1980s and early 1990s. Dr. Boudjema Menhour has a PhD in Organic Chemistry and is a researcher at the Institute of Molecular Chemistry, Reims (ICMR), University of Reims Champagne-Ardenne, Reims, France. He research interests include developing a synthesis of carbohydrate analogues, targeting a specific activity, such as immunostimulatory, and eliciting properties. Claire Coiffier, PhD, is a researcher at the Institute of Molecular Chemistry, Reims (ICMR), University of Reims Champagne-Ardenne, Reims, France. She has worked on the top-down approach for the synthesis of biologically active substrates and on the analysis of preferred conformations of C-furanosides, using theoretical chemistry.

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