Effects of nitrogen and alkene substitution on the PtCl2 catalyzed cycloisomerization of N-tethered 1,6-enyne precursors to the triple reuptake inhibitor GSK1360707

The effects of nitrogen and alkene substitution on the cycloisomerization of N-tethered 1,6-enynes into 3-azabicyclo[4.1.0]heptene precursors to the triple reuptake inhibitor GSK1360707 are described. In general, electron donating substituents proved beneficial both in terms of the reaction rate and chemoselectivity.     

Vibroacoustic characteristics of a gothic harp

The "gothic" style of harp was popular across most of Europe from the late medieval period to the Renaissance. These harps have a one-piece, longitudinally oriented hardwood soundboard, as opposed to the transverse-oriented bonded softwood structure on a modern instrument. In addition, the one-piece back is flexible, whereas the back of a modern instrument is a rigid molded shell. To study the gothic harp, one was constructed from plans created by the Boston Museum of Fine Arts from a late German model in their collection. The vibrational behaviors of the soundboard and soundbox were measured at various stages of construction. The completed instrument was subjected to modal analysis and radiativity measurements. The sound radiation is dominated by two breathing modes at 188 and 273 Hz, each with strong motion of the back, and modes around 350 Hz. Taken together, these modes function like the A0/T1 resonance pairs seen in the soundboxes of other instruments, and a comparison is made with the guitar. Also observed is that as the frequency increases, radiation is emitted from higher up the soundboard, and from higher soundholes. This feature has been observed in other harps, and is a consequence of the harp family's unique geometry.     

Evaluation of Energy Balance in a Batch and Circulating Non-thermal Plasma Reactors During Organic Pollutant Oxidation in Aqueous Solution

Plasma Chemistry and Plasma Processing - This work presents the treatment of an organic waste solution using gliding arc plasma in moist air, which is an excellent source of oxidizing species....     

On the strong liouville property for co-compact Riemannian covers

This note discusses the existence of non-negative non-constant harmonic functions on co-compact covers with linear deck group. Conferenza tenuta da P. Bougerol il 4 ottobre 1993     

Sets of degrees of computable fields

Given a Σ₂ (resp. Σ₁) degree of recursive unsolvability a, a computable field (resp. a computable field with a splitting algorithm)F is constructed in any given characteristic, such that the set of dimensions of all finite extensions ofF has degree a. This is part of an M.Sc. Thesis presented at The Hebrew University. The author wishes to express his indebtedness to his Supervisor Professor H. Gaifman for his constant guidance and encouragement. Thanks are also due to Professor G. Sabbagh (University of Paris VII) for several useful suggestions.     

Barbatusin and cyclobutatusin,two novel diterpenoids from coleus barbatus bentham

The structure of three diterpenoids from Coleus barbatus, Bentham (Labiatae) having a spirocyclopropyl side chain have been determined: they are barbatusin (1a), 3β-hydroxy-3-deoxybarbatusin (2) and cyclobutatusin (3a). The structures of 1a and 3a were established by X-ray diffraction analysis, and the latter compound has been shown to have an unusual 4-membered ring produced by a bond across C(1) to C(11). Chemical transformations and interconversions are presented, together with spectroscopic studies.     

Aminomethyl-bipyridine bearing two flexible nitronyl-nitroxide arms: a new podand for complexation of transition metals in a facial or meridional conformation

Transition metal complexes of 6-aminomethyl-bis[methyl-2-(4,5-dihydro-4,4,5,5- tetramethylimidazolinyl-3-oxide-l-oxy)]-2,2'-bipyridine, bpyN(NIT)(2), 1, have been synthesized and characterized by FAB-MS, UV-vis, FT-IR, and EPR spectroscopies, elemental analysis, and susceptibility measurements. Single-crystal X-ray diffraction studies have been performed on all compounds giving the following crystal data: bpyN(NIT)(2), 1, triclinic, P(-)1, Z = 2, a = 10.7224(4) A, b = 11.0995(4) A, c = 13.1134(3) A, alpha = 114.101(9) degrees, beta = 97.476(9) degrees, gamma = 99.667(9) degrees; ZnbpyN(NIT)(2), 2, hexagonal, P3(2), Z = 3, a = 15.4545(3) A, b = 15.4545(3) A, c = 13.5594(3) A; NibpyN(NIT)(2), 3, hexagonal, P3(2), Z = 3, a = 15.2867(1) A, b = 15.2867(1) A, c = 13.7160(1) A; CubpyN(NIT)(2), 4, triclinic, P(-)l, Z = 2, a = 11.8640(4) A, b = 13.2023(4) A, c = 13.2661(5) A, alpha = 90.539(9) degrees, beta = 104.983(9) degrees, gamma = 113.252(9) degrees. The two radicals of the free ligand 1 are almost perpendicular to one another in the solid state, favoring a weak ferromagnetic interaction (J/k(B) = 8.8 K). The complexes obtained by wrapping the ligand around a single metal center gave rise to two different coordination schemes where the two radicals of 1 adopt a ON(3)O meridional (with Ni and Zn) or a ON(3)O facial conformation (with Cu), which strongly affects the magnetic and electronic properties (O accounts for the coordinated oxygen atoms of the nitroxide radicals and N(3) accounts for the tertiary amine). For 2, a model of a dimer has been used giving rise to a weak antiferromagnetic interaction between the radicals (J/k(B) = -5.3 K). For 3, a very strong intramolecular antiferromagnetic coupling has been found and estimated at J/k(B) = -230 K and J'/k(B) = -110 K between the nickel and each radical using an asymmetric model of a trimer. For 4, an unusual magnetic behavior is observed, dominated by antiferromagnetic interactions with a residual plateau at chiT = 0.63 emu.K.mol(-)(1). Molecular modeling at the CASSCF level is in keeping with an antiferromagnetic coupling of the radical bound with the Cu(II) in the equatorial position. The combined structural, electronic, and magnetic characteristics suggest that the use of a flexible molecule provide an additional approach for fine-tuning magnetic interactions.     

A practical synthesis of ethyl 1,2,4-triazole-3-carboxylate and its use in the formation of chiral 1′,2′-seco-nucleosides of ribavirin

A practical and efficient synthesis of ethyl 1,2,4-triazole-3-carboxylate ( 6a , R' = H) from ethyl carboethoxyformimidate hydrochloride ( 7 ) is described. Alkylation of this heterocycle with the chloromethyl ethers of 1,3-O-dibenzylbutane-1,2R,3S-triol ( 8a ) and 1,3,4-O-tribenzylbutane-1,2R,3S,4-tetrol ( 8b ), followed by conversion of the ester function to the amide and deprotection, furnished the chiral 1′,2′-seco-nucleosides of ribavirin, 11a and 11b , respectively.     

Some models for evaluating the cavity formation energies in liquids

In the mixing process of solutes into solvents, the cavity formation energy is generally introduced into the energy balance. In this study, models for calculating this type of energy are proposed. These models are based on the Hansen's partial solubility parameters δ_d (MPa^1/2) dispersive, δ_p (MPa^1/2) polar and δ_h (MPa^1/2) hydrogen-bonding, and on the internal pressure P_j (J cm^?3) of the solvents.     

First enantioselective synthesis and determination of the absolute configuration of natural (+)-dehydro-β-monocyclonerolidol

The enantioselective synthesis and determination of the absolute configuration of (+)-dehydro-β-monocyclonerolidol, a natural product isolated from the liverwort P. subobtusa, has been achieved starting from (+)-karahana lactone as an enantiopure building block. Furthermore, the methodology applied provided a new approach towards the known (+)-γ-cyclohomocitral, a key intermediate in the sequence, and natural (+)-pallescensone.