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Chiral building blocks for macrolides and related natural products are obtained from 1,6-anhydrosugars by conversion of the bicyclic acetals 2 or 12 into the open chain chiral 1,3-dithianes 6 and 13. Branched precursors can be obtained by opening of the ?erný epoxide 1 with the 1,3-dithiane anion to yield 7, followed by ring opening with 1,3-propanedithiol to the bis-1,3-dithiane 8.  相似文献   
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Electrophilic trisubstituted ethylenes, ring-disubstituted ethyl 2-cyano-3-phenyl-2-propenoates, RPhCH?C(CN)CO2C2H5 (where R is 3-Br-4-CH3O, 5-Br-2-CH3O, 3-F-2- CH3, 3-F-4-CH3, 4-F-2-CH3, 4-F-3-CH3, 5-F-2-CH3, 2-Cl-5-NO2, 2-Cl-6-NO2, 4-Cl-3- NO2) were prepared and copolymerized with styrene. The monomers were synthesized by the piperidine catalyzed Knoevenagel condensation of ring-disubstituted benzaldehydes and ethyl cyanoacetate, and characterized by CHN analysis, IR, 1H and 13C-NMR. All the ethylenes were copolymerized with styrene (M1) in solution with radical initiation (ABCN) at 70°C. The composition of the copolymers was calculated from nitrogen analysis, and the structures were analyzed by IR, 1H and 13C-NMR. The order of relative reactivity (1/r 1) for the monomers is 5-Br-2-CH3O (1.02) > 4-Cl-3-NO2 (0.93) > 3-F-4-CH3 (0.81) > 2-Cl-6-NO2 (0.77) > 2-Cl-5-NO2 (0.71) > 3-Br-4-CH3O (0.66) > 4-F-3-CH3 (0.60) > 3-F-2-CH3 (0.38) > 4-F-2-CH3 (0.31) > 5-F-2-CH3 (0.16). Relatively high Tg of the copolymers in comparison with that of polystyrene indicates a decrease in chain mobility of the copolymer due to the high dipolar character of the trisubstituted ethylene monomer unit. Decomposition of the copolymers in nitrogen occurred in two steps, first in the 250–500°C range with residue (2–26% wt.), which then decomposed in the 500–800°C range.  相似文献   
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[reaction: see text] Fully protected triphenylmethyl 2-O-mesyl-1-thio-beta-d-gluco- (14) and -alpha-d-mannopyranoside (28) were transformed by a stereoselective intramolecular 1 --> 2 trans-arylthio migration into methyl 2-S-triphenylmethyl-alpha-d-manno- (15) and -beta-d-glucopyranoside (29), respectively, using NaOCH(3) as nucleophile. The 2-S-triphenylmethyl ethers (15 and 29) were directly oxidized to sugar 2-C-sulfonic acids by using oxone (2KHSO(5), KHSO(4), K(2)SO(4)). Compounds (21, 23, 32, and 35) are the first representatives of secondary sugar C-sulfonic acids.  相似文献   
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Gehle  R. W.  Masri  S. F. 《Nonlinear dynamics》1998,17(1):77-94
This study presents a practical, fieldable active controller applicable to shallow, slack cables. The controller is based upon an underlying theory that does not assume that the inertial forces are negligible in the direction of the cable chord. The theoretical framework is developed, and an experimental verification is presented. The experiments utilized a TV camera to track a small number of LED targets on the controlled cable, a commercial X-Y tracker and a PC to compute the cable's present position and velocity, and a linear actuator to vary the cable's tension. A Kalman filter was employed to smooth the position estimates and provide least-squares estimates of the cable velocity. The stability limits for the phase and amplitude of the control signal were established. An analytical estimate of the induced damping expected from the control algorithm is derived. Experimental measurements of the cable frequency and induced damping compared well with theoretical predictions. It is shown that he proposed active control approach is a simple, reliable, as well as an effective, method for vibration attenuation in lightly damped, shallow, slack cables.  相似文献   
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A synthesis of a new alkaloid-fullerene conjugate (1) is reported. The reaction was carried out by photoinduced [3+2] cycloaddition of the Alstonia indole alkaloid, 6,7-seco-angustilobine B (2), to fullerene[C60] (3) under aerobic conditions. The major monoaddition photoadduct (1) was characterized unambiguously by UV, IR, MALDI-TOFMS and NMR experiments. A mechanism highlighted by sequential photoinduced electron transfer andradical recombination pathways is also proposed. No significant enhancement in inhibition against M. tuberculosis H37Rv was observed for 1 compared with its parent compounds 2 and 3.  相似文献   
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