Stereoselective synthesis of (±)-palitantin

Stereoselective synthesis of (±)-palitantin has been completed.     

Designing magnetics of capped perpendicular media with minor-loop analysis

A novel method of analyzing the switching field distribution (SFD) and magnetic correlation length of perpendicular magnetic recording media that uses major and minor magnetization loops is proposed. By applying the analysis to a series of capped perpendicular media, we found that a thick capping layer with a low saturation magnetization effectively reduced SFD without rapidly increasing the magnetic correlation length. Transmission electron microscope observation suggests that the SFD is narrowed by the increased uniformity of intergranular exchange coupling via the thick capping layer. Evaluations of recording characteristics demonstrated a close correlation between narrower SFDs and improved recording performance. Reducing exchange coupling dispersion is a clear solution for improving the performance of recording media.     

Fast polarimetry system for the application to spin quantum non-demolition measurement

We report the development of a fast pulse polarimeter for the application to quantum non-demolition measurement of atomic spin (spin QND). The developed system was tunable to the atomic resonance of a ytterbium atom and has narrow laser line width suitable for spin QND. Using the developed polarimeter, we successfully demonstrated the measurement of the vacuum noise, with 10⁶ to 10⁷ photon number per pulse. PACS 42.25.Ja; 42.50.Lc; 42.55.Px     

Polarization in projectile fragmentation andg-factor measurements for neutron-rich nuclei

A method to produce beams of polarized unstable nuclei was developed, which fully exploits the advantageous features of the projectile fragmentation reaction. The method was applied tog-factor measurements of several neutron-rich nuclei. We present experimental results so far obtained and discuss capabilities and limitations the present polarization method has.     

Two New Syntheses of the Pyranojuglone Pigment α-Caryopterone

By a simple process, 3-methoxyjuglone (= 8-hydroxy-2-methoxy-1,4-naphthoquinone; 9 ) has been synthesized from 1,2,4-trimethoxybenzene ( 5 ) and converted, after prenylation, to α-caryopterone ( 1 ; Scheme 1), a pyranojuglone pigment from Caryopteris clandonensis. On the other hand, juglone (= 5-hydroxy-1,4-naphthoquinone; 12 ) was regioselectively prenylated at C(2) via its 1-methoxy-cyclohexa-1,3-diene adduct 15 (Scheme 2). The 2-prenyljuglone ( 4 ) thus formed led to 1 after oxidation and other reactions.     

Stereoselective synthesis of (±)-senepoxyde and (±)-crotepoxide1

Stereoselective synthesis of (±)-senepoxyde and (±) crotepoxide is described starting from 2-hydroxymethyl-1, 4-benzoquinone through the retro-Diels-Alder reaction.     

Twelve new compounds from Ligularia melanothyrsa; isolation of melanothyrsins A–E,normelanothyrsin A,and other eremophilane sesquiterpenoids

Twelve new compounds, namely, five melanothyrsins A–E (1α-angeloyloxyeremophilenolides), normelanothyrsin A (1α-angeloyloxynoreremophilenone), and six other eremophilane-type compounds, have been isolated from Ligularia melanothyrsa Hand.-Mazz. (Asteraceae), collected in the Sichuan Province of China. Six of the compounds have a 1α-angeloyloxy moiety, while the other six have no functional group at the C-1 position. The absolute configuration was also determined using CD spectra. This is the first chemical study of compounds isolated from this species.     

Study of the dissociation of a charge-reduced phosphopeptide formed by electron transfer from an alkali metal target

Doubly protonated phosphopeptide (YGGMHRQET(p)VDC) ions obtained by electrospray ionization were collided with Xe and Cs targets to give singly and doubly charged positive ions via collision-induced dissociation (CID). The resulting ions were analyzed and detected by using an electrostatic analyzer (ESA). Whereas doubly charged fragment ions resulting from collisionally activated dissociation (CAD) were dominant in the CID spectrum with the Xe target, singly charged fragment ions resulting from electron transfer dissociation (ETD) were dominant in the CID spectrum with the Cs target. The most intense peak resulting from ETD was estimated to be associated with the charge-reduced ion with H2 lost from the precursor. Five c-type fragment ions with amino acid residues detached consecutively from the C-terminal were clearly observed without a loss of the phosphate group. These ions must be formed by N--Calpha bond cleavage, in a manner similar to the cases of electron capture dissociation (ECD) and ETD from negative ions. Although the accuracy in m/z of the CID spectra was about +/-1 Th because of the mass analysis using the ESA, it is supposed from the m/z values of the c-type ions that these ions were accompanied by the loss of a hydrogen atom. Four z-type (or y--NH3, or y--H2O) ions analogously detached consecutively from the N-terminal were also observed. The fragmentation processes took place within the time scale of 4.5 micros in the high-energy collision. The present results demonstrated that high-energy ETD with the alkali metal target allowed determination of the position of phosphorylation and the amino acid sequence of post-translational peptides.     

An SOS-QE Approach to Nonlinear Gain Analysis for Polynomial Dynamical Systems

Combined use of the method of sum of squares (SOS) and quantifier elimination (QE) is discussed with regard to the problem of nonlinear gain analysis for a class of dynamical systems. SOS, a numerical method, is used to search for the structure of a gain function quickly, and QE, a symbolic method, determines all gain functions in the structure to find the minimum gain function. QE can also be used for the infeasibility check of gain structures. A proposed analysis procedure for polynomial dynamical systems prevents unnecessary searching for a gain structure. Two illustrative examples show the effectiveness of the proposed gain analysis procedure.