Compiles current tested and proven approaches to synthesize novel nucleoside analogues Featuring contributions from leading synthetic chemists from around the world, this book brings together and describes tested and proven approaches for the chemical synthesis of common families of nucleoside analogues. Readers will learn to create new nucleoside analogues with desired therapeutic properties by using a variety of methods to chemically modify natural nucleosides, including:
Changes to the heterocyclic base Modification of substituents at the sugar ring Replacement of the furanose ring by a different carbo- or heterocyclic ring Introduction of conformational restrictions Synthesis of enantiomers Preparation of hydrolitically stable C-nucleosides Chemical Synthesis of Nucleoside Analogues covers all the major classes of nucleosides, including pronucleotides, C-nucleosides, carbanucleosides, and PNA monomers which have shown great promise as starting points for the synthesis of nucleoside analogues. The book also includes experimental procedures for key reactions related to the synthesis of nucleoside analogues, providing a valuable tool for the preparation of a number of different compounds.
Throughout the book, chemical schemes and figures help readers better understand the chemical structures of nucleoside analogues and the methods used to synthesize them. Extensive references serve as a gateway to the growing body of original research studies and reviews in the field.
Synthetically modified nucleosides have proven their value as therapeutic drugs, in particular as antiviral and antitumor agents. However, many of these nucleoside analogues have undesirable side effects. With Chemical Synthesis of Nucleoside Analogues as their guide, researchers have a new tool for synthesizing a new generation of nucleoside analogues that can be used as therapeutic drugs with fewer unwanted side effects.
Biocatalytic methodologies for selective modified nucleosides
Miguel Ferrero Fuertes, Susana Fernández González, Vicente Gotor Fernández
págs. 1-48
págs. 49-102
págs. 103-162
Phosphonated nucleoside analogues
Roberto Romeo, Caterina Carnovale, Antonio Rescifina, Maria Assunta Chiacchio
págs. 163-208
págs. 209-228
págs. 229-262
Omar Boutureira Martin, Maria Isabel Matheu Malpartida, Yolanda Díaz Giménez, Sergio Castillón Miranda
págs. 263-316
págs. 317-344
Synthesis of conformationally constrained nucleoside analogues
Esma Maougal, Jean Marc Escudier, Christophe Len, Didier Dubreuil, Jacques Lebreton
págs. 345-426
Synthesis of 3'-Spiro-Substituted nucleosides: chemistry of TSAO nucleoside derivatives
María José Camarasa Ríus, Sonsoles Velázquez Díaz, Ana Rosa San Félix, María Jesús Pérez Pérez
págs. 427-472
págs. 473-534
págs. 535-604
Uncommon Three-, four-, and six-membered nucleosides
E. Groaz, Piet Herdewijn
págs. 605-654
Recent Advances in synthesis and biological activity of 4'-Thionucleosides
Varughese A. Mulamoottil, Mahesh S. Majik, Girish Chandra, Lak Shin Jeong
págs. 655-698
Recent advances in the chemical synthesis of Aza-Nucleosides
Tomás Tejero López, José Ignacio Delso Hernández, Pedro Merino Filella
págs. 699-726
págs. 727-780
págs. 781-818
págs. 819-846
págs. 847-880
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