Abstract
GlucoSiFA derivatives bearing an azide or alkynyl side chain were obtained from peracetyl- d -glucose using as key step a tosylate substitution by a SiFA thiolate obtained from 4-(di- tert -butylfluorsilyl)benzenethiol. In analogy, two-fold SiFA-substituted maltose and lactose derivatives were synthesized via bistosylates. Introduction of an acetal-protecting group in β- d -azidolactose allowed the synthesis of a LactoSiFA derivative bearing only one SiFA moiety.
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Wiegand, A., Wiese, V., Glowacki, B., Iovkova, L., Schirrmacher, R., Jurkschat, K., & Krause, N. (2019). GlucoSiFA and LactoSiFA: New Types of Carbohydrate-Tagged Silicon-Based Fluoride Acceptors for 18 F-Positron Emission Tomography (PET). Synthesis (Germany), 51(5), 1196–1206. https://doi.org/10.1055/s-0037-1611656
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