Chemical Synthesis of Nucleoside Analogues
Published on 19. February 2013
Software
Other digital
912 pages
978-1-118-49808-8 (ISBN)
Description
Chemical Synthesis of Nucleoside Analogues examines the application of synthetic methodologies to the preparation of compounds of biological interest, including the synthesis of nucleic acids on pre-existing nucleic acid templates, assembling RNA, or DNA. This comprehensive compendium culls expert contributions that highlight the structural components of nucleosides (supported by spectral data) and their modification as well as the synthetic strategies based on chemical approaches. The text serves undergraduate students, specialists, and researchers, allowing access to a variety of compounds without forgetting the biological importance of the target compounds.
More details
Language
English
Place of publication
New York
United States
Target group
Professional and scholarly
College/higher education
Dimensions
Height: 185 mm
Width: 135 mm
Thickness: 5 mm
Weight
2 gr
ISBN-13
978-1-118-49808-8 (9781118498088)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Classification
Other editions
Additional editions
Pedro Merino
Chemical Synthesis of Nucleoside Analogues
E-Book
02/2013
Wiley
€170.99
Available for download
Pedro Merino
Chemical Synthesis of Nucleoside Analogues
E-Book
02/2013
Wiley
€175.99
Available for download
Content
Foreword Preface Contributors 1. Deoxynucleoside analogues (50 pp) Prof. Vicente Gotor, University of Oviedo. Spain 2. Nucleosides modified at the base moiety (50 pp) Prof. Luigi Agrofoglio, University of Orleans. France 3. Acyclic Nucleosides (50 pp) Prof. Antonin Holy, Academy of Sciences of the Czech Republic 4. Phosphorylated nucleoside analogues (40 pp) Prof. Giovanni Romeo, University of Messina. Italy 5. Triphosphorylated nucleoside analogues (20 pp) Prof. Chris Meier, University of Hamburg. Germany 6. Pro-nucleotides (30 pp) Prof. Christian Perigaud, University of Montpellier 2. France 7. C-Nucleosides (50 pp) Prof. Sergio Castillon, University Rovira i Virgili. Spain 8. Isonucleosides (30 pp) Prof. Vasu Nair, University of Georgia. USA 9. Conformationally constrained nucleosides (40 pp) Prof. Jacques Lebreton, University of Nantes. France 10. Spironucleosides (30 pp) Prof. Maria Jose Camarasa, Spanish Council of Scientific Research. Spain 11. L-nucleosides (30 pp) Dr. Daniela Perrone, University of Ferrara. Italy 12. Carbocyclic Nucleosides (60 pp) Dr. Eric Leclerc, University of Rouen. France 13. Uncommon three-, four and six-membered nucleosides (40 pp) Dr. Elisabetta Groaz, University of Leuven. Belgium 14. Thionucleosides (25 pp) Prof. L. S. Jeong, Ewha University. South Korea 15. Azanucleosides and related compounds (40 pp) Prof. Tomas Tejero, University of Zaragoza. Spain 16. Oxathiolane and dioxolane nucleosides (30 pp) Dr. Annalisa Guaragna, University of Napoli. Italy 17. Isoxazolidinyl nucleosides (30 pp) Prof. Ugo Chiacchio, University of Catania. Italy 18. Nucleoside antibiotics (40 pp) Prof. Apurba Dutta, University of Kansas. USA 19. Building blocks for peptide nucleic acids (30 pp) Prof. Pedro Merino, University of Zaragoza. Spain Index