Mostrando 81 - 100 Resultados de 11,307 Para Buscar '"A. D."', tiempo de consulta: 0.19s Limitar resultados
  1. 81
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  4. 84
    “…This work implements the general Quantum Annealer Eigensolver (QAE) algorithm to solve the molecular electronic Hamiltonian eigenvalue-eigenvector problem on a D-Wave 2000Q quantum annealer. The approach is based on the matrix formulation, efficiently uses qubit resources based on a power-of-two encoding scheme and is hardware-dominant relying on only one classically optimized parameter. …”
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  5. 85
    “…In this work, we demonstrate the use of a D-Wave quantum annealer for the calculation of excited electronic states of molecular systems. …”
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  6. 86
  7. 87
    “…Four new heptaketides, pseudonectrins A–D (1–4), and four known compounds (5–8) were isolated from cultures of an endophytic fungus Nectria pseudotrichia. …”
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  8. 88
  9. 89
    “…We experimentally explore a novel approach to this problem by using a D-Wave quantum annealer, benchmarking its performance for attaining a financial equilibrium. …”
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  10. 90
  11. 91
    Libro
  12. 92
    Publicado 1971
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  13. 93
    por Gordon, A. D.
    Publicado 1999
    Libro
  14. 94
    “…Structural tailoring has been made at the donor and acceptor units of two recently synthesized quinoline–carbazole molecules (Q1, Q2) and acceptor–donor–π–acceptor (A–D–π–A) and donor–acceptor–donor–π–acceptor (D–A–D–π–A) type novel molecules Q1D1–Q1D3 and Q2D2–Q2D3 have been quantum chemically designed, respectively. …”
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  15. 95
    Publicado 1989
    Libro
  16. 96
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  18. 98
    “…METHODS AND FINDINGS: The prospective multicenter study CryptoA/D was designed in France (1997–2001) to analyse the factors influencing clinical presentation and outcome without the bias of inclusion into therapeutic trials. …”
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  19. 99
  20. 100
    “…Six regioisomers associated with the tricyclic core of thiaplakortones A–D have been synthesized. Reaction of 1H-indole-4,7-dione and 1-tosyl-1H-indole-4,7-dione with 2-aminoethanesulfinic acid afforded a regioisomeric series, which was subsequently deprotected and oxidized to yield the tricyclic core scaffolds present in the thiaplakortones. …”
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