Software reliability assessment models based on cumulative bernoulli trial processes

The binomial software reliability growth model (SRGM) contains most existing SRGMs proposed in earlier work as special cases, and can describe every software failure-occurrence pattern in continuous time. In this paper, we propose generalized binomial SRGMs in both continuous and discrete time, based on the idea of cumulative Bernoulli trials. It is shown that the proposed models give some new unusual discrete models as well as the well-known continuous SRGMs. Through numerical examples with actual software failure data, two estimation methods for model parameters with grouped data are provided, and the predictive model performance is examined quantitatively.     

Phase type approximation for optimal auto-sleep scheduling

This paper addresses the problem of how to determine optimal sleep timing when the computer user should turn the hard disk or the display off in order to save electric power after the computer has not been used. We propose a stochastic model to obtain an optimal sleep timing strategy which minimizes the expected power consumed per unit time in the steady state, where access requirements of the system occur in a renewal process and processing is described by a general service time. Phase type approximation is proposed to represent the expected power consumed per unit time. We investigate the performance of this approximation through a simulation study, and design an optimal auto-sleep schedule for a computer workstation system using real data.     

A generalized discrete-time order replacement model

In this article, we consider a discrete-time order replacementproblem. More precisely, we treat a generalized model with morecomplex cost structure than Kaio & Osaki (1979, IEEE Trans.Reliab., R-29, 405–406) and with two decision variables:allowable inventory time and ordering time. Based on the discreteprobabilistic argument, we derive the optimal ordering policyto deliver a spare unit preventively by a regular order, soas to minimize the expected cost per unit time in the steadystate. Numerical examples are devoted to carrying out the sensitivityanalysis of model parameters on the optimal ordering policyand its associated expected cost value.     

Convenient use of ortho-formylphenyl thioglycoside for regioselective conjugation with glycosyl acceptors towards regioselective 1,2-cis-glycosylation

A facile methodology is proposed for regioselective conjugation between glycosyl donors and acceptors towards the development of regioselective 1,2-cis-glycosylation method. ortho-Formylphenyl 1-thio-β-d-galactopyranoside was regioselectively tethered to methyl α-d-glucopyranoside under acidic condition to furnish an 4,6-O-arylidene acetal-linked conjugate. This conjugate can be readily converted to an ether-linked 4-O- or 6-O-derivative by regioselective cleavage of the acetal ring. In the glycosylation reaction, the ether-linked 4-OH conjugate was found to show excellent 1,2-cis selectivity via an intramolecular 1,9-transfer.     

Efficient N-arylation of azole compounds utilizing selective aryl-transfer TMP-iodonium(III) reagents

It was determined that diaryliodonium(III) triflates bearing a trimethoxybenzene (TMP) auxiliary are more reactive than the reported selective aryl-transfer iodonium salts in the N-arylation of benzimidazoles and other types of azole compounds under catalytic conditions. The TMP-iodonium(III) salts can thus effectively facilitate the reaction at 50?°C or below, producing the corresponding N-arylated biaryls without the formation of TMP-derived coupling byproducts. Utilization of this TMP reagent under mild conditions would prevent the underlying problem of participation of the auxiliary group in the coupling reactions, which is observed while using the iodonium(III) salts that require elevated temperatures.     

Recyclable synthesis of mesityl iodonium(III) salts

An efficient protocol for C–H condensation of hypervalent iodine compounds toward arenes in fluoroalcohols has been applied to the recyclable preparation of mesityl iodonium(III) salts. The electrophilicities of [hydroxy(tosyloxy)iodo]mesitylene (MesI(OH)OTs) and iodomesitylene diacetate (MesI(OAc)₂) are suitably enhanced in 2,2,2-trifluoroethanol. A series of nucleophilic aromatic compounds react smoothly with MesI(OH)OTs and MesI(OAc)₂ or in situ hypervalent iodine(III) species, generated from iodomesitylene, to provide the target mesityl iodonium(III) salts in good yields at room temperature with broad functional group tolerance. This C–H condensation strategy merits high para-regioselectivities during the diaryliodonium(III) salt formation, but the major limitation in the case of low-reactive aromatic substrates is byproduct formation resulting from the self-condensation of the nucleophilic mesitylene ring in MesI(OH)OTs and MesI(OAc)₂.     

Three-dimensional display with a long viewing distance by use of integral photography

We developed a technique of three-dimensional (3-D) display for distant viewing of a 3-D image without the need for special glasses. The photobased integral photography (IP) method allows precise 3-D images to be displayed at long viewing distances without any influence from deviated or distorted lenses in a lens array. We calculate elemental images from a referential viewing area for each lens and project the corresponding result images to photographic film through each lens. We succeed in creating an image display that appears to have three dimensionality even when viewed from a distance, with an image depth of 5.7 m or more in front of the display and 3.5 m or more behind the display. To the best of our knowledge, the long-distance IP display presented here is technically unique because it is the first report of generation of an image with such a long viewing distance.     

An easy access to halide ion-catalytic alpha-glycosylation using carbon tetrabromide and triphenylphosphine as multifunctional reagents

The reaction of a 2-O-benzyl-1-hydroxy sugar with CBr4 and Ph3P generates a glycosyl bromide in situ, which is coupled with an acceptor alcohol in the presence of N,N-tetramethylurea to afford an alpha-glycosyl product virtually quantitatively. In a proposed pathway, the reagent combination plays multiple roles such as the generation of a glycosyl donor, the activation of glycosylation, and the dehydration of the reaction system. These roles allow a simple alpha-glycosylation to be performed without special attention to dehydration. Various alpha-glycosyl (D-gluco-, D-galacto- and L-fuco-) products including glycosyl glycerols and cholesterols have been prepared with this method.