629 research outputs found

    Procedimiento de preparación de derivados de tipo arilo-heteroarilo y arilo-arilo y compuestos obtenidos

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    El objeto de la presente invención es un procedimiento de preparación de derivados de tipo arilo — heteroarilo y arilo - arilo a partir de anilinas o sales de diazonio y de compuestos aromáticos, que pueden ser arilos o heteroarilo, en el cual se utilizan materiales que aportan ácido ascórbico o sus derivados como catalizadores. Constituyen igualmente un objeto de la presente invención los compuestos obtenidos mediante el referido procedimiento.Peer reviewedConsejo Superior de Investigaciones CientíficasA1 Solicitud de adición a la patent

    Molecular Simplification in Bioactive Molecules: Formal Synthesis of (+)-Muconin

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    7 páginas, 1 figura, 7 esquemas, 1 tabla.-- El PDF es la versión post-print.The concept of molecular simplification as a drug design strategy to shorten synthetic routes, while keeping or enhancing the biological activity of the lead drug, has been applied to (+)-muconin, an acetogenin with remarkable cytotoxicity. A novel approach that enables the stereoselective synthesis of such a natural compound or its enantiomer from a common precursor is described. An additional advantage of the method is complete stereochemical control and the decrease in the number of chemical steps required, thus providing an enhancement of the overall yield. Antiproliferative studies against the human solid tumor cell lines showed that the aliphatic chain-THF/THP fragment of (+)-muconin has modest cytotoxic activity. The strategy opens the way to preparing novel bioactive acetogenin analogues by shorter synthetic routes.The authors thank the MYCT (PPQ2002- 04361-C04-02) of Spain and the Canary Islands Government for supporting this research. F.R.P.C. thanks CajaCanarias for a FPI fellowship. R.C. thanks the Spanish MEC for a FPU fellowship. J.M.P. thanks ICIC for a postdoctoral fellowship.Peer reviewe

    It’s a Wonderful Life

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    It’s a Wonderful Life

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    Online Coalition Formation under Random Arrival or Coalition Dissolution

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    Coalition formation considers the question of how to partition a set of nn agents into disjoint coalitions according to their preferences. We consider a cardinal utility model with additively separable aggregation of preferences and study the online variant of coalition formation, where the agents arrive in sequence and whenever an agent arrives, they have to be assigned to a coalition immediately. The goal is to maximize social welfare. In a purely deterministic model, the greedy algorithm, where an agent is assigned to the coalition with the largest gain, is known to achieve an optimal competitive ratio, which heavily relies on the range of utilities. We complement this result by considering two related models. First, we study a model where agents arrive in a random order. We find that the competitive ratio of the greedy algorithm is Θ(1n2)\Theta\left(\frac{1}{n^2}\right), whereas an alternative algorithm, which is based on alternating between waiting and greedy phases, can achieve a competitive ratio of Θ(1n)\Theta\left(\frac{1}{n}\right). Second, we relax the irrevocability of decisions by allowing to dissolve coalitions into singleton coalitions, presenting a matching-based algorithm that once again achieves a competitive ratio of Θ(1n)\Theta\left(\frac{1}{n}\right). Hence, compared to the base model, we present two ways to achieve a competitive ratio that precisely gets rid of utility dependencies. Our results also give novel insights in weighted online matching.Comment: Appears in the 31st Annual European Symposium on Algorithms (ESA 2023
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