Fully automated polymer-assisted synthesis of 1,5-biaryl pyrazoles

The polymer-assisted solution-phase (PASP) synthesis of a 192-member 2-D array of 1,5-biaryl pyrazoles 4[1-12,1-16] is reported. The synthesis was performed in a fully automated manner using a multiprobe top-filtration robot and incorporates a "catch and release" step to afford library compounds directly in high yield and purity.     

Hydrodynamics of a bounded vertical film with nonlinear surface properties

The drainage of a thin liquid film with an insoluble monolayer down a vertical wall is studied. Lubrication theory is used to develop a model where the film is pinned at the top with a given thickness and the film drains into a bath at the bottom. A nonlinear equation of state is used for the surface tension and the surface viscosity is a nonlinear function of the surfactant concentration; these are appropriate for some aqueous systems. The three partial differential equations are solved via discretization in space and then the resulting differential algebraic system is solved. Results are described for a wide range of parameters, and the conditions under which the free surface is immobilized are discussed.     

The heats of reaction of phosphines and phosphites with toluene-molybdenum tricarbonyl. Importance of both steric and electronic factors in determining the Mo---PR3 bond strength

The heats of reaction of tolueneMo(CO)₃ with a series of phosphines and phosphites have been measured by solution calorimetry. The order of stability toward formation of fac-(PR₃)₃Mo(CO)₃ in THF solution is: P(OCH₃)₃s> PMe₃ > PⁿBu₃ > PMe₂Ph> PEt₃ > triphos> P(OPh)₃ > PMePh₂ > PPh₃ > PCl₃ and spans a range of 25 kcal/mol reflecting individual bond strength differences up to 8 kcal/mol. The bulky phosphines PCy₃ and P^tBu₃ react with tolueneMo(CO)₃ in THF, but 30–40 kcal/mol less heat is evolved in these reactions than with the other phosphines and phosphites. The coordinately unsaturated five-coordinate complexes (PR₃)₂Mo(CO)₃ are proposed as the reaction products. The importance of both steric and electronic factors in the Mo---P bond is discussed.     

Poly(choloyl)-based amphiphiles as pore-forming agents: transport-active monomers by design

This paper describes the design and synthesis of a family of pore-forming amphiphiles. Two of these amphiphiles, which are derived from cholic acid, lysine, and p-phenylenediamine, can produce pores in lipid bilayers as individual molecules. In sharp contrast, analogous amphiphiles that do not contain a rigid 1,4-phenylenediamide moiety favor the formation of dimer-based pores. Kinetic evidence in support of monomer- and dimer-based pores has been obtained from Na+ transport measurements across bilayers made from 1-palmitoyl-2-oleoyl-2-sn-glycero-3-phosphocholine (POPC). Structure-activity studies that have been carried out with pore-forming, dimer-based amphiphiles have also revealed a significant activity dependence on their overall compactness. The practical potential of pore-forming amphiphiles with controllable supramolecular properties is briefly discussed.     

Unusual regiochemistry in a beckmann-like rearrangement of camphor. α-Camphidone via methylene migration.

Reaction of camphor with hydroxylamine-O-sulfonic acid affords the nitrogen insertion product α-camphidone by migration of the methylene group rather than the bridgehead. Since Beckmann rearrangements of trigonal oximes afford bridgehead cleavage products with camphor, an alternative synchronous rearrangement of a tetrahedral intermediate is proposed for this Beckmann-like reaction.     

Synthesis of homoceramides, novel ceramide analogues, and their lack of effect on the growth of hippocampal neurons

The synthesis of a new series of D-erythro-homoceramide analogues is described. Several synthetic approaches were investigated. Homoceramides can be successfully synthesized from L-homoserine as chiral building block and a protected Weinreb-amide as a key intermediate. The synthesis of short-chain analogues with a heptyl side chain, as well as with a phenyl residue in the sphingoid part (instead of the naturally occurring tridecyl side chain), was effected. The homoceramides 15-17 and 24 were investigated for their potential to reverse the inhibitory effect of fumonisin B(1) on axonal growth. Unfortunately, none of the tested compounds showed any biological activity due to their lack of metabolism to glucosylhomoceramide.     

Synthesis and characterisation of phosphane-substituted Co3C clusters having a pendant allyl side-chain

Substituted μ₃-carbido-capped tricobalt carbonyl clusters have been synthesised by reaction of [Co₃(μ₃-C(O)OCH₂CHCH₂)(CO)₉] with a range of monodentate and chelating phosphane ligands. The products have been characterised by microanalysis, IR and NMR spectroscopy, mass spectrometry and, in the case of [Co₃(μ₃-CR)(CO)₇(dppe)], [Co₃(μ₃-CR)(CO)₇(dppm)], [Co₃(μ₃-CR)(CO)₇(PPh₃)₂], [Co₃(μ₃-CR)(CO)₇(PMe₃)₂] and [Co₃(μ₃-CR)(CO)₆(PEt₃)₃] (R=C(O)OCH₂CHCH₂), single crystal X-ray diffraction.     

A host-guest complex between a metal-organic cyclotriveratrylene analog and a polyoxometalate: [Cu6(4,7-phenanthroline)8(MeCN)4]2PM12O40(M = Mo or W)

The synthesis and crystal structure of Cu(6)(4,7-phenanthroline)(8)(MeCN)(4)(6+) a novel Cu(i)-molecular hexamer is described in which the metal cations and phenanthroline molecules self-assemble into a dimer of shallow triangular-shaped bowls, within which are located large spherical polyoxometalate anions PM(12)O(40)(3-)(M = Mo or W).     

Synthesis of methyl-1,6-dioxaspiro[4,5]decanes using organoselenium mediated cyclization reactions

Three naturally occurring methyl-1,6-dioxaspiro[4.5]decanes have been prepared in good yield using organoselenium mediated reactions during the crucial cyclization process.