Interactions between 4-thiothymidine and water-soluble cyclodextrins: Evidence for supramolecular structures in aqueous solutions

• Vito Rizzi,
• Sergio Matera,
• Paola Semeraro,
• Paola Fini and
• Pinalysa Cosma

Beilstein J. Org. Chem. 2016, 12, 549–563, doi:10.3762/bjoc.12.54

• complexation mode of the inclusion complexes involving 4-thiothymidine (S4TdR, a known photosensitizer) and five CDs, namely 2-hydroxypropyl-α-cyclodextrin (2-HP-α-CD), 2-hydroxypropyl-β-cyclodextrin (2-HP-β-CD), 2-hydroxypropyl-γ-cyclodextrin (2-HP-γ-CD), heptakis-(2,6-di-O-methyl)-β-cyclodextrin (DIMEB CD

• potential method to improve/change the photochemical behavior of the thiobase. In particular, the protection of S4TdR, as photosensitizer, from degradation through reactive oxygen species during photodynamic therapy applications could be attained in the presence of all analyzed CDs. A study in this

Stereoselective synthesis of hernandulcin, peroxylippidulcine A, lippidulcines A, B and C and taste evaluation

• Marco G. Rigamonti and
• Francesco G. Gatti

Beilstein J. Org. Chem. 2015, 11, 2117–2124, doi:10.3762/bjoc.11.228

• [32] of (+)-hernandulcin in a mixed solvent system (CH2Cl2/MeOH, 4:1) and in presence of a catalytic amount of the methylene blue photosensitizer (<0.1% in weight, λ = 280 nm) afforded a mixture of peroxylippidulcines A, B and C, i.e., 2a–c, in the ratio of 47:21:32 (by 1H NMR) and in an almost

Effective ascorbate-free and photolatent click reactions in water using a photoreducible copper(II)-ethylenediamine precatalyst

• Redouane Beniazza,
• Natalia Bayo,
• Florian Molton,
• Carole Duboc,
• Stéphane Massip,
• Nathan McClenaghan,
• Dominique Lastécouères and
• Jean-Marc Vincent

Beilstein J. Org. Chem. 2015, 11, 1950–1959, doi:10.3762/bjoc.11.211

• water in the absence of sodium ascorbate is an active area of current research with strong potential for applications in bioconjugation. The water-soluble and photoreducible copper(II)–EDA (EDA = ethylenediamine) complex 1, which has two 4-benzoylbenzoates acting as both counterion and photosensitizer

• photogenerated copper(I) being very reactive. On irradiating aqueous reaction mixtures containing 1 mol % of 1 at 365 nm (TLC lamp) for 1 h, click reactions were shown to proceed to full conversion. Keywords: benzophenone photosensitizer; bioconjugation; click chemistry; copper; photoreduction; Introduction

• tren (tren = tris(2-aminoethyl)amine) ligand derivative [11][12] or the dmeda (dmeda = N,N’-dimethylethylenediamine) ligand [13][14] (Scheme 1). Irradiation at 365 nm of the benzophenone photosensitizer (n→π* electronic transition), introduced through the carboxylate counterion, mediated a highly

The synthesis of active pharmaceutical ingredients (APIs) using continuous flow chemistry

• Marcus Baumann and
• Ian R. Baxendale

Beilstein J. Org. Chem. 2015, 11, 1194–1219, doi:10.3762/bjoc.11.134

• -polymer tubing wrapped around a cooled medium pressure mercury lamp was used to efficiently generate and react the singlet oxygen in the presence of tetraphenylporphyrin (TPP) as a photosensitizer. Upon exiting the photoreactor, the reaction stream was acidified by combining with a stream of TFA in order

An integrated photocatalytic/enzymatic system for the reduction of CO₂ to methanol in bioglycerol–water

• Michele Aresta,
• Angela Dibenedetto,
• Tomasz Baran,
• Antonella Angelini,
• Przemysław Łabuz and
• Wojciech Macyk

Beilstein J. Org. Chem. 2014, 10, 2556–2565, doi:10.3762/bjoc.10.267

• photosensitizer by injecting electrons into the conduction band of titania [20]. Photocatalytic tests of NADH regeneration using these materials have been performed using visible light irradiation (λ > 400 nm). The results are summarized in Figure 3. Figure 3a shows that the conversion yield of NAD+ into NADH is

• described in this paper consists of the use of visible light and the coupling of an inexpensive photocatalyst with robust e−- and H−-transfer mediators, which can be used for days. Furthermore, we have demonstrated the entire mechanism of the electron flow from the photo-excited photosensitizer to NAD

A versatile δ-aminolevulinic acid (ΑLA)-cyclodextrin bimodal conjugate-prodrug for PDT applications with the help of intracellular chemistry

• Chrysie Aggelidou,
• Theodossis A. Theodossiou,
• Antonio Ricardo Gonçalves,
• Mariza Lampropoulou and
• Konstantina Yannakopoulou

Beilstein J. Org. Chem. 2014, 10, 2414–2420, doi:10.3762/bjoc.10.251

• , molecular/drug carrier with the capacity to undergo intracellular transformation into protoporphyrin IX (PpIX), an endogenous powerful photosensitizer for photodynamic therapy (PDT). The water-soluble derivative 2 was prepared by esterifying δ-azidolevulinic acid with heptakis(6-hydroxyethylamino-6-deoxy)-β

• cancerous rather than squamous tissues [1]. δ-Aminolevulinic acid (1, ALA, Scheme 1) is a δ-amino acid precursor in the cellular biosynthesis of heme [2]. The penultimate step in this biosynthetic cycle is the iron chelation of protoporphyrin IX (PpIX), a porphyrin photosensitizer (PS) which was shown to be

• ) cleavable ester bonds expected to release 1 by the action of intracellular enzymes. Taken together, the strategy would combine prodrug photosensitizer capability with molecular/drug transport in a single versatile bimodal system. Results and Discussion Synthesis: The suitable β-CD derivative to be linked

Tailoring of organic dyes with oxidoreductive compounds to obtain photocyclic radical generator systems exhibiting photocatalytic behavior

• Christian Ley,
• Julien Christmann,
• Ahmad Ibrahim,
• Luciano H. Di Stefano and
• Xavier Allonas

Beilstein J. Org. Chem. 2014, 10, 936–947, doi:10.3762/bjoc.10.92

• spectral limitation, Type II PIS were developed. They contain the photosensitizer (PS) which absorbs the light and a coinitiator (Co) which reacts with PS excited states through hydrogen abstraction or electron transfer reaction (see Scheme 1). Numerous dyes were reported as PS [9][27][28][29][30][31][32

• photosensitizer (PS) molecules present (NPS) to the total number of absorbed photons (Nabs). It could be expressed by the following equation: where V is the volume of the irradiated solution. The absorbed photon concentration is given by: where I0 is the incident light intensity on the cell (9 mW·cm−3, i.e., 4·10

• system The Type II system studied here contains only RB as photosensitizer and an electron acceptor TA (or donor EDB). Both RB/TA and RB/EDB systems were calculated. Figure 4 shows the changes in RB, RB•+, TA, and TA•− concentrations for the former system. Two important conclusions are to be outlined

Synthesis of nucleotide–amino acid conjugates designed for photo-CIDNP experiments by a phosphotriester approach

• Tatyana V. Abramova,
• Olga B. Morozova,
• Vladimir N. Silnikov and
• Alexandra V. Yurkovskaya

Beilstein J. Org. Chem. 2013, 9, 2898–2909, doi:10.3762/bjoc.9.326

• which pronounced CIDNP effects could be detected [13]. Tryptophan was found as one of the most efficient reducing agents for different protonated forms of oxidized guanosine 5′-monophosphate in a wide pH range [14]. The 2,2’-dipyridyl dye, which is used as a photosensitizer in most of our TR CIDNP

• photosensitizer) and CIDNP kinetics of the photoreactions of conjugates 7 or 8 under the same conditions. Synthesis of model compounds for time resolved photo-CIDNP NMR experiments It is easy to notice that conjugates 1–8 are designed as a kind of di- and trimer nucleotide species. So, the key points of its

Interplay of ortho- with spiro-cyclisation during iminyl radical closures onto arenes and heteroarenes

• Roy T. McBurney and
• John C. Walton

Beilstein J. Org. Chem. 2013, 9, 1083–1092, doi:10.3762/bjoc.9.120

• -furanylphenylethanone and 1,3-diphenylpropan-1-one. Ring closures of aryl-iminyl radicals Individual members of the set of substituted biphenyl O-ethoxycarbonyl oximes 1a–f were UV irradiated for 3 h at ambient temperature in deoxygenated benzotrifluoride solutions with 1 equiv wt/wt of MAP as a photosensitizer. As

Triple-channel microreactor for biphasic gas–liquid reactions: Photosensitized oxygenations

• Ram Awatar Maurya,
• Chan Pil Park and
• Dong-Pyo Kim

Beilstein J. Org. Chem. 2011, 7, 1158–1163, doi:10.3762/bjoc.7.134

• channel was used for the flow of the reaction solution containing the reactant and a photosensitizer, whereas the outer two channels were used for oxygen supply (Figure 3). Efficient oxygen supply to the reaction mixture was achieved by adjustment of the pressure in the outer channels. The overpressure of

Photosonochemical catalytic ring opening of α-epoxyketones

• Hamid R. Memarian and
• Ali Saffar-Teluri

Beilstein J. Org. Chem. 2007, 3, No. 2, doi:10.1186/1860-5397-3-2

• . [7][8][9][10][11][12][13][14][15][16][17] It is well known that the substituted pyridinium cations are good electron acceptors. [18] Garcia and coworkers have used N-alkyl-2,4,6-triphenylpyridinium tetrafluoroborate as photosensitizer in the photochemical cyclization of 5-methyl-4-hexenoic acid to