<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns="http://purl.org/rss/1.0/" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <channel rdf:about="https://ria.asturias.es/RIA/handle/123456789/1">
    <title>DSpace Community:</title>
    <link>https://ria.asturias.es/RIA/handle/123456789/1</link>
    <description />
    <items>
      <rdf:Seq>
        <rdf:li rdf:resource="https://ria.asturias.es/RIA/handle/123456789/6501" />
        <rdf:li rdf:resource="https://ria.asturias.es/RIA/handle/123456789/10445" />
        <rdf:li rdf:resource="https://ria.asturias.es/RIA/handle/123456789/10447" />
        <rdf:li rdf:resource="https://ria.asturias.es/RIA/handle/123456789/8188" />
      </rdf:Seq>
    </items>
    <dc:date>2026-01-04T13:34:43Z</dc:date>
  </channel>
  <item rdf:about="https://ria.asturias.es/RIA/handle/123456789/6501">
    <title>“ἔπεα πτερόεντα”, una fórmula homérica recurrente</title>
    <link>https://ria.asturias.es/RIA/handle/123456789/6501</link>
    <description>Title: “ἔπεα πτερόεντα”, una fórmula homérica recurrente
Authors: Torre Beivide, Abigail
Description: Para este trabajo subimos dos archivos, uno con la comunicación y otro con un PowerPoint en el que se pueden encontrar los textos a los que se remite.</description>
    <dc:date>2015-04-15T00:00:00Z</dc:date>
  </item>
  <item rdf:about="https://ria.asturias.es/RIA/handle/123456789/10445">
    <title>Zinc‐Catalyzed Synthesis of Conjugated Dienoates through Unusual Cross‐Couplings of Zinc Carbenes with Diazo Compounds</title>
    <link>https://ria.asturias.es/RIA/handle/123456789/10445</link>
    <description>Title: Zinc‐Catalyzed Synthesis of Conjugated Dienoates through Unusual Cross‐Couplings of Zinc Carbenes with Diazo Compounds
Authors: Mata García, Sergio; Vicente Arroyo, Rubén; López García, Luis Ángel; Gonzalez Rodríguez, Maria José; González Martínez, Jesús
Abstract: Zinc‐catalyzed selective cross‐coupling of two carbene sources, such as vinyl diazo compounds and enynones, enabled the synthesis of conjugated dienoate derivatives. This reaction involved the unprecedented coupling of a zinc furyl carbene with vinyl diazo compounds through the γ‐carbon. Alternatively, dienoates were also prepared by a commutative cross‐coupling of zinc vinyl carbenes generated from cyclopropenes and simple diazo compounds.
Description: En este artículo de investigación se describe el acoplamiento cruzado catalizado por cloruro de zinc entre diazocompuestos y   vinil diazocompuestos con distintos precursores de carbenos como son los ciclopropenos y eninonas.</description>
    <dc:date>2016-11-30T00:00:00Z</dc:date>
  </item>
  <item rdf:about="https://ria.asturias.es/RIA/handle/123456789/10447">
    <title>Zinc-Catalyzed Synthesis of Allylsilanes via Si–H Bond Insertion of Vinyl Carbenoids Generated from Cyclopropenes</title>
    <link>https://ria.asturias.es/RIA/handle/123456789/10447</link>
    <description>Title: Zinc-Catalyzed Synthesis of Allylsilanes via Si–H Bond Insertion of Vinyl Carbenoids Generated from Cyclopropenes
Authors: Mata García, Sergio; Vicente Arroyo, Rubén; López García, Luis Ángel
Abstract: Allylsilanes have long been recognized as valuable building blocks for organic synthesis. A zinc‐catalyzed reaction of cyclopropenes and hydrosilanes provides a convenient route to these versatile unsaturated organosilanes. In this transformation, ZnBr2 serves as an efficient catalyst, allowing the generation of a zinc vinyl carbenoid intermediate, which is subsequently involved in a Si−H bond insertion. The process shows broad scope, and is amenable to substituted and functionalized cyclopropenes or the functionalization of polysiloxanes. Moreover, zinc‐catalyzed carbene insertion into a Ge−H bond is reported for the first time.
Description: En este artículo de investigación se describe una metodología catalítica para la síntesis de alilsilanos a partir de ciclopropenos en presencia de cantidades catalíticas de bromuro de zinc.</description>
    <dc:date>2017-05-10T00:00:00Z</dc:date>
  </item>
  <item rdf:about="https://ria.asturias.es/RIA/handle/123456789/8188">
    <title>Zinc-Catalyzed Multicomponent Reactions: Easy Access to Furyl- Substituted Cyclopropane and 1,2-Dioxolane Derivatives</title>
    <link>https://ria.asturias.es/RIA/handle/123456789/8188</link>
    <description>Title: Zinc-Catalyzed Multicomponent Reactions: Easy Access to Furyl- Substituted Cyclopropane and 1,2-Dioxolane Derivatives
Authors: López García, Luis Ángel; Vicente Arroyo, Rubén; González, Jesús
Abstract: An efficient synthesis of furyl-substituted&#xD;
cyclopropane derivatives through a zinc-catalyzed three component&#xD;
coupling of 1,3-dicarbonyl compounds, alkynals and alkenes are described.On the other hand, the synthesis  of 1,2-dioxolane derivatives through a zinc-promoted aerobic&#xD;
oxidation of cyclopropane derivatives has been also developed.&#xD;
A four-component process yielding these cyclic peroxide&#xD;
derivatives has been also realized.
Description: Reacciones multicomponentes catalizadas por sales de zinc. Acceso a ciclopropilfuranos y derivados de 1,2-dioxolanos.</description>
    <dc:date>2016-04-27T00:00:00Z</dc:date>
  </item>
</rdf:RDF>

