16.17. 7 Purines (Update 2020)
Book
Editors: Christmann, M.; Huang, Z.; Jiang, X.; Li, J.-J.; Oestreich, M.; Petersson, E. J.; Schaumann, E.; Wang, M.
Title: Knowledge Updates 2020/1
Print ISBN: 9783132435582; Online ISBN: 9783132435605; Book DOI: 10.1055/b000000102
1st edition © 2020 Thieme. All rights reserved.
Georg Thieme Verlag KG, Stuttgart
Subjects: Organic Chemistry;Chemical Reactions, Catalysis;Organometallic Chemistry;Laboratory Techniques, Stoichiometry
Science of Synthesis Knowledge Updates
Parent publication
Title: Science of Synthesis
DOI: 10.1055/b-00000101
Series Editors: Fürstner, A. (Editor-in-Chief); Carreira, E. M.; Faul, M.; Kobayashi, S.; Koch, G.; Molander, G. A.; Nevado, C.; Trost, B. M.; You, S.-L.
Type: Multivolume Edition
Abstract
This chapter is an update to the earlier Science of Synthesis contribution (Section 16.17) describing methods for the synthesis and chemical modification of purine and purine derivatives. It focuses on the literature published in the period 2002–2019, with a particular emphasis on regioselective direct C—H functionalization of purines, transition-metal-catalyzed cross-coupling reactions of halopurines, and synthesis of purine analogues, including azidopurines, by exchange of substituents.
Key words
adenines - alkenylation - alkylation - alkynylation - amination - arylation - azidopurines - Buchwald–Hartwig reaction - carbon–carbon coupling - C-H bond activation - click reactions - cross-coupling reactions - cyclization - double C-H activation - fluorination - fused purines - guanines - halogen-exchange reactions - halogenation - halopurines - hypoxanthines - imidazoles - Negishi coupling - nucleosides - organometallic reagents - palladium catalysts - purines - pyrimidines - radical reactions - ring closure - Sonogashira coupling - Stille coupling - Suzuki–Miyaura coupling - transition metals- 11 Pineda de las Infantas y Villatoro MJ, Unciti-Broceta JD, Contreras-Montoya R, Garcia-Salcedo JA, Gallo Mezo MA, Unciti-Broceta A, Diaz-Mochon JJ. Sci. Rep. 2015; 5: 9139
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