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Beilstein J. Org. Chem. 2016, 12, 391–405, doi:10.3762/bjoc.12.42
Graphical Abstract
Scheme 1: Reaction of trimethylsilyl cyanide with tricarbonyl (η5-cyclohexadienyl)iron(1+) salts. Reproduced ...
Figure 1: (a) Supramolecular pore formers. Reproduced with permission from [6]. Copyright 1990 Elsevier. (b) Uni...
Figure 2: An intelligent liquid crystal to read out saccharide structure as a color-change. Picture provided ...
Scheme 2: Polymeric boronic acid receptor units developed by Wulff. Reproduced from [16]. Copyright 1982 Internat...
Figure 3: Fluorescence photoinduced electron transfer (PET) pH sensor developed by A. P. De Silva.
Figure 4: Fluorescence PET sensor for saccharides.
Figure 5: (a) Glucose selective PET system. (b) Chiral discriminating PET system.
Figure 6: (a) Fluorescence photoinduced electron transfer (PET) cation sensors developed by A. P. De Silva. (...
Figure 7: (a) Pyrene diboronic acids (n = 3–8). (b) Pyrene monoboronic acid. (c) Block chart showing the rela...
Figure 8: Glysure Continuous Intravascular Glucose Monitoring (CIGM) System. Image provided by Nicholas P. Ba...
Figure 9: Chiral discrimination of D- and L-tartaric acid by (R)-8 at pH 5.6. [(R)-8] = 5.0 × 10−6 mol dm−3, ...
Figure 10: Chiral discriminating sensor (relative stereochemistry shown) constructed using a good fluorophore ...
Figure 11: Fluorescence emission intensity-pH profile of: (a) Sensor 15: 1.0 × 10−6 mol dm−3 (λex 370 nm, λem ...
Figure 12: Modular chiral discriminating d-PET systems (relative stereochemistry shown).
Figure 13: With Matthew Davidson and Steven Bull during “World Cup” lecture tour of Japan in 2002. (Left) Priv...
Figure 14: Preparation of chiral boron reagent and use as catalyst for aza-Diels–Alder reactions.
Figure 15: Chiral three component self-assembling system.