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21.
Raghunath O. Ramabhadran Mohamed Husaini bin Abdul Rahman Steven J. Collier Richard C. Storr Roderick W. Bates 《Tetrahedron》2018,74(1):1-5
Trapping of a pyrimidinone-derived o-quinodimethane with tetraphenylcyclopentadienone gives a mixture of the [4 + 2] and formal [4 + 4] adducts. Computational studies show that the latter arises by a sequence of [4 + 2] cycloaddition, homolysis, radical recombination to a spiro-tetrahydrofuran and Claisen rearrangement under the thermolytic conditions. 相似文献
22.
Formal syntheses of lasubine II and subcosine II have been completed by the synthesis of epi-lasubine II. The synthesis involves diastereoselective allylation of a methoxy isoxazolidine and a tandem hydrogenation process leading stereoselectively to a trisubstituted piperidine. 相似文献
23.
G. R. Bates 《Journal of Optimization Theory and Applications》1978,24(4):639-649
Lower closure theorems are proved for optimal control problems governed by ordinary differential equations for which the interval of definition may be unbounded. One theorem assumes that Cesari's property (Q) holds. Two theorems are proved which do not require property (Q), but assume either a generalized Lipschitz condition or a bound on the controls in an appropriateL
p-space. An example shows that these hypotheses can hold without property (Q) holding. 相似文献
24.
It is found that the forced common turning point procedure is satisfactory for treating the excitation of hydrogen atoms by slow protons evan at an energy of relative motion as low as 30 eV. 相似文献
25.
Karen A. Switek Kwanho Chang Frank S. Bates Marc A. Hillmyer 《Journal of polymer science. Part A, Polymer chemistry》2007,45(3):361-373
Block copolymers containing polystyrene and polycyclooctene were synthesized with a ring‐opening metathesis polymerization/chain‐transfer approach. Polystyrene, containing appropriately placed olefins, was prepared by anionic polymerization and served as a macromolecular chain‐transfer agent for the ring‐opening metathesis polymerization of cyclooctene. These unsaturated polymers were subsequently converted to the corresponding saturated triblock copolymers with a simple heterogeneous catalytic hydrogenation step. The molecular and morphological characterization of the block copolymers was consistent with the absence of significant branching in the central polycyclooctene and polyethylene blocks [high melting temperatures (114–127 °C) and levels of crystallinity (17–42%)]. A dramatic improvement in both the long‐range order and the mechanical properties of a microphase‐separated, symmetric polystyrene–polycyclooctene–polystyrene block copolymer sample was observed after fractionation. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 361–373, 2007 相似文献
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Conductance measurements of 12 quaternary ammonium salts in propylene carbonate (PC) have been made at 25°C. The cations were either tetramethylammonium, tetraethylammonium, or tetra-n-butylammonium, and the concentrations of salt varied from about 2×10–4 to 5×10–3
M. The data were analyzed by the equation of Pitts. The results showed that the benzoate, nitrobenzoate, and pentachlorophenolate salts are completely dissociated. The nitrophenolate, chlorophenolate, methylsulfonate, and nitrate salts are only slightly associated (K
A
from 2.5 to 6.5), while the acetate, phenylacetate, and nitrophenolate salts display somewhat more extensive association, with ionpair association constants from 17 to 45. Limiting molar conductances for the anions were derived. The factors affecting ionic mobilities in this dipolar aprotic solvent are discussed.On leave 1973–1975 from the University of Gdask, Poland. 相似文献
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