A mild and general method for the synthesis of 2-substituted-5-hydroxypyrimidines

5-Bromopyrimidines are converted to 5-hydroxypyrimidines using a mild synthetic procedure. The method is general and can be applied to compounds containing functional groups which are not compatible with the other reagents previously available for this conversion.     

Citrafungins A and B, two new fungal metabolite inhibitors of GGTase I with antifungal activity

[structure: see text] Screening of natural products extracts led to the discovery of citrafungins A and B, two new fungal metabolites of the alkylcitrate family that are inhibitors of GGTase I of various pathogenic fungal species with IC(50) values of 2.5-15 microM. These compounds exhibited antifungal activities with MIC values of 0.40-55 microM. The isolation, structure elucidation, relative and absolute stereochemistry, and biological activities of citrafungins are described.     

Racemic atropisomeric N,N-chelate ligands for recognizing chiral carboxylates via Zn(II) coordination: structure, fluorescence, and circular dichroism

Two racemic atropisomeric N,N'-chelate ligands, bis{3,3'-[N-Ph-2-(2'-py)indolyl]} (1) and bis{3,3'-N-4-[N-2-(2'-py)indolyl]phenyl-2-(2'-py)indolyl} (2), have been found to be able to distinguish the enantiomers of Zn((R)-BrMeBu)2 and Zn((S)-BrMeBu)2 where BrMeBu = O2CCH(Br)CHMe2, with a distinct and intense CD spectral response at approximately the 10 microM concentration range. Computational studies established that the (R)-1-Zn((R)-BrMeBu)2 or (S)-1-Zn((S)-BrMeBu)2 diastereomer is more stable than (R)-1-Zn((S)-BrMeBu)2 or (S)-1-Zn((R)-BrMeBu)2. In addition, computational studies showed that the CD spectra of (S)-1-Zn((S)-BrMeBu)2 and (S)-1-Zn((R)-BrMeBu)2 are similar. (1)H NMR spectra confirmed that these two diastereomers exist in solution in about a 2:1 ratio for both complexes of 1 and 2. The distinct CD response of the racemic ligands 1 and 2 toward the chiral zinc(II) carboxylate is therefore attributed to the preferential formation of one diastereomer. The binding modes of the zinc(II) salt with ligands 1 and 2 were established by the crystal structures of the model compounds 1-Zn(tfa)2 and 2-Zn(tfa)2 (tfa = CF3CO2(-)), where the Zn(II) ion is chelated by the two central pyridyl groups in the ligand. Fluorescent titration experiments with various zinc(II) salts showed that the fluorescent spectrum of the atropisomeric ligand displays an anion-dependent change. The zinc(II) binding strength to the N,N'-chelate site of the atropisomeric ligand has been found to play a key role in the selective recognition of different chiral zinc(II) carboxylate derivatives by the racemic atropisomeric ligands.     

Determination of metal ion content of beverages and estimation of target hazard quotients: a comparative study

Background  

Considerable research has been directed towards the roles of metal ions in nutrition with metal ion toxicity attracting particular attention. The aim of this study is to measure the levels of metal ions found in selected beverages (red wine, stout and apple juice) and to determine their potential detrimental effects via calculation of the Target Hazard Quotients (THQ) for 250 mL daily consumption.     

Implementation of dynamical nucleation theory effective fragment potentials method for modeling aerosol chemistry

In this work, the dynamical nucleation theory (DNT) model using the ab initio based effective fragment potential (EFP) is implemented for evaluating the evaporation rate constant and molecular properties of molecular clusters. Predicting the nucleation rates of aerosol particles in different chemical environments is a key step toward understanding the dynamics of complex aerosol chemistry. Therefore, molecular scale models of nanoclusters are required to understand the macroscopic nucleation process. On the basis of variational transition state theory, DNT provides an efficient approach to predict nucleation kinetics. While most DNT Monte Carlo simulations use analytic potentials to model critical sized clusters, or use ab initio potentials to model very small clusters, the DNTEFP Monte Carlo method presented here can treat up to critical sized clusters using the effective fragment potential (EFP), a rigorous nonempirical intermolecular model potential based on ab initio electronic structure theory calculations, improvable in a systematic manner. The DNTEFP method is applied to study the evaporation rates, energetics, and structure factors of multicomponent clusters containing water and isoprene. The most probable topology of the transition state characterizing the evaporation of one water molecule from a water hexamer at 243 K is predicted to be a conformer that contains six hydrogen bonds, with a topology that corresponds to two water molecules stacked on top of a quadrangular (H(2)O)(4) cluster. For the water hexamer in the presence of isoprene, an increase in the cluster size and a 3-fold increase in the evaporation rate are predicted relative to the reaction in which one water molecule evaporates from a water hexamer cluster.     

Full Characterization and some reactions of 1‐(2‐adamantyl)‐3‐(1‐adamantyl)aziridin‐2‐one

We found that 1‐(2‐adamantyl)‐3‐tert‐butylaziridin‐2‐one ( 5a ) is unstable. It slowly decomposes at room temperature, although detectable by IR spectroscopy (1840 cm^?1 band in CCl₄). On the other hand, a closely related analogue, 1‐(2‐adamantyl)‐3‐(1‐adamantyl)aziridin‐2‐one ( 5b ), is very stable, in concurrence with an earlier report [1]. We fully characterized aziridinone 5b , identified its thermal decomposition products ( 7 and 8 ) and reacted it with two aprotic ionic (tBuO^? and HO^?) and one protic non‐ionic nucleophile (benzylamine). All three products ( 9b , 10 , and 11 ) result from exclusive cleavage of the lactam (1‐2) bond.     

Parallel algorithm for integral transformations and GUGA MCSCF

Summary An algorithm for the parallelization of the atomic to molecular integral transformation and the subsequent steps in a GUGA based MCSCF calculation is presented. Timing data shows that the transformation and diagonalization steps are well parallelized and that several of the other portions of the MCSCF code are moderately parallel. Remaining sequential bottlenecks are identified.     

Efficacy of different targeting agents in the photolysis of interleukin-2 receptor bearing cells

The multichain interleukin-2 receptor (IL-2R) has been proposed as a target for immunotherapy in the treatment of certain cancers including adult T-cell leukemia and cutaneous T-cell lymphoma as well as certain autoimmune diseases. The IL-2R is abnormally expressed on cells associated with each of these diseases; while normal, non-activated T-cells do not express the receptor. This report describes the selective photolysis of activated and non-activated IL-2R expressing cells using several immunoconjugates synthesized with one of two photosensitizers, hematoporphyrin (HP) or chlorin-e(6) (Ce(6)), covalently linked to IL-2 or an anti-IL-2R antibody. Destruction of IL-2R bearing cells was achieved after photosensitizer internalization and irradiation using all tested photosensitizer conjugates. Chlorin containing conjugates were more effective, by a factor of 4 or more, than HP containing conjugates. Conjugates made with IL-2 were up to 30 times more effective than conjugates that used a monoclonal antibody against the IL-2R for targeting. Activation of the cells to increase IL-2R expression decreased the internalization time required for optimal therapeutic efficacy; however, stimulation of the cell to increase IL-2 secretion greatly reduced conjugate effectiveness. This work could lead to the development of more effective strategies to treat T-cell diseases.     

K2NdP2S7: A Mixed‐Valent Neodymium(III) Thiophosphate According to K4Nd2[PS4]2[P2S6] with Discrete [PS4]3– and [S3P–PS3]4– Anions

Pale blue, lath‐shaped single crystals of K₂NdP₂S₇ (≡ K₄Nd₂[PS₄]₂[P₂S₆]; monoclinic, P2₁/n, a = 904.76(8), b = 677.38(6), c = 1988.7(2) pm, β = 97.295(5)°, Z = 2) are obtained by the reaction of Nd, S and P₂S₅ with an excess of KCl as a flux in evacuated silica tubes at 750 °C (7 d) which should produce Nd[PS₄] instead. Beside isolated [PS₄]^3– tetrahedra, the crystal structure contains discrete ethane‐analogous [P₂S₆]^4– (≡ [S₃P–PS₃]^4–) units in staggered conformation with tetravalent phosphorus cations and a P–P distance of 219 pm. The two crystallographically different potassium cations show coordination numbers of nine and ten in the shape of distorted mono‐ and bicapped square antiprisms. Finally, the Nd³⁺ cations are surrounded by eight sulfur atoms arranged as (uncapped) square antiprisms. The entire structure is dominated by (K1)⁺ containing {(Nd₂[PS₄]₂[P₂S₆])^4–} layers parallel (101) which are three‐dimensionally interconnected by (K2)⁺ cations.