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D Pletcher

Publications and source records attributed to D Pletcher.

3 recordsLinked to original sources

MINERVA: a multi-modality plugin-based radiation therapy treatment planning system.

Researchers at the INEEL, MSU, LLNL and UCD have undertaken development of MINERVA, a patient-centric, multi-modal, radiation treatment planning system, which can be used for planning and analysing several radiotherapy modalities, either singly or combined, using common treatment planning tools. It employs an integrated, lightweight plugin architecture to accommodate multi-modal treatment planning using standard interface components. The design also facilitates the future integration of improved planning technologies. The code is being developed with the Java programming language for interoperability. The MINERVA design includes the image processing, model definition and data analysis modules with a central module to coordinate communication and data transfer. Dose calculation is performed by source and transport plugin modules, which communicate either directly through the database or through MINERVA's openly published, extensible markup language (XML)-based application programmer's interface (API). All internal data are managed by a database management system and can be exported to other applications or new installations through the API data formats. A full computation path has been established for molecular-targeted radiotherapy treatment planning, with additional treatment modalities presently under development.

Body Burden↗

Electrosyntheses from aromatic aldehydes in a flow cell. Part I. The reduction of benzaldehyde.

The reduction of benzaldehyde in acidic water-methanol mixtures has been re-investigated in a membrane flow cell with a lead cathode with the objective of defining conditions where le- reduction occurs and the C6H5CH.OH radical intermediate is formed in high selectivity. It is shown that it is the cathode potential which controls the ratio of le-/2e- product (i.e. hydrobenzoin to benzyl alcohol) and a high rate generation of the radicals is also favoured by an efficient mass transport regime.

Benzaldehydes↗

Electrosyntheses from aromatic aldehydes in a flow cell. Part II. The cross-coupling of benzaldehydes to unsymmetrical diols.

It is demonstrated that the reduction of mixtures of two benzaldehydes in acidic water-methanol in a membrane flow cell with a lead cathode can lead to a mixture of diols including the unsymmetrical diol, e.g. 4-F-C6H4-CH(OH)-CH(OH)-C6H5. In the conditions employed, the ratio of the three diol products follows the statistical distribution expected for the coupling of two different radical intermediates produced in the same ratio as the concentrations of their precursors. The yield and current efficiency for the diols are excellent when the pH and potential are selected so that a le- reduction of both benzaldehydes occurs. The yield of unsymmetrical dimer based on one reactant can be increased substantially by using the other carbonyl compound as a sacrificial reagent.

Acetophenones↗