The local time of self-intersections of Brownian motions as generalized Brownian functionals

In this Letter, we show that the local time of self-intersections ofd-dimensional Brownian motions is a generalized Brownian functional in the sense of Hida.     

1-Phosphacephalosporin. I. Synthesis of racemic 7-unsubstituted-1-phosphadethia-3-cephem 1-oxides

The novel unnatural ring system, 1-phosphacephalosporin, was synthesized for the first time from 4-acetoxy-2-azetidinone.     

Efficient N-sulfenylation of 2-azetidinones using S-substituted thiophthalimides

Reaction of N-unsubstituted β-lactams with various S-substituted thiophthalimides provides an efficient route to the corresponding N-thio-2-azetidinones.     

Time-resolved ESR study of the lowest excited triplet states of para-quinones in glassy matrices at 77 k

The lowest excited nπ* triplet of 9.10-anthraquinone, 1.4-naphthoquinone and 1,4-benzoquinone were studied in glassy matrices at 77 K using a time-resolved ESR method. The D value of the triplet state of 9,10-anthraquinone varied from ?0.351 cm^?1 in a polar solvent to ?0.318 cm^?1 in a non-polar solvent. Both 1,4-naphthoquinone and 1,4-benzoquinone in polar solvents showed triplet state spectra with a D value of ?0.330 cm^?1. A computer simulation revealed the existence of widely distributed zero-field splitting parameters in the glassy condition. These data are compared with an analysis of CIDEP results of para-quinones.     

The primary fragmentation step of isoxazole upon electron impact. A correlation with photochemistry

Three isomeric compounds, I, II and III, were prepared and their mass spectra recorded. Comparisons of the spectra showed that the fragmentation of I proceeds only by way of II, and that II itself is transformed in part to III upon electron impact. It is suggested that selective ionization of each one of the two isolated functional groups in II may afford two isomeric radical ions, IIa and IIb. A possible interrelation to the photochemistry of these compounds is also discussed.     

High-performance gel filtration of water-soluble samples on polyvinyl alcohol columns

The chromatographic behaviour in aqueous solution of pullulans, polyethylene glycols, peptides and proteins with different molecular weights on newly developed polyvinyl alcohol columns (Asahipak GS column series: GS-310, GS-320, GS-510 and GS-520) has been investigated. Pullulans and polyethylene glycols eluted according to the gel filtration mode, so both series of compounds produced almost equal calibration curves for GS-310 and GS-320 and for GS-510 and GS-520; the exclusion limits on GS-310 and GS-320 and on GS-510 and GS-520 were found to be ca. 40,000 and 300,000, respectively. Peptides and proteins were found to adsorb slightly on the columns. However, the plots of the elution volumes against the logarithm of the molecular weights for many of the substrates tested gave rise to the linear calibration curves. Recovery of several crude proteins was also studied for the columns and high values were obtained (81–100%). The effects of changes in the flow-rate, temperature and concentration of electrolytes added to the eluents, on the retention of all four types of compound are also reported.     

Role of hydroxyl groups in the stereochemistry of hydrogen transfer from chiral NAD(P)H model to carbonyl

Asymmetric reduction of α-ketoester with a chiral dihydronicotinamide was significantly affected by chiral aromatic additives, capable of exerting an attractive interaction with dihydropyridine ring, which was further consolidated through with magnesium.     

A peptide motif recognizing a polymer stereoregularity

A combinatorial phage display method was applied to films composed of a stereoregular polymer of methacrylates. The phage clones with selective affinity for isotactic (it) poly(methyl methacrylate) (PMMA) were isolated. Greater amounts of the phage clones bound to it-PMMA, compared to other stereoregular PMMAs. The phage expressing ELWRPTR most strongly bound to the polymer, and the selectivity was also the best. The peptide motif essential for the specific interaction with the stereoregular polymer was revealed.