<?xml version="1.0" encoding="UTF-8"?>
<feed xmlns="http://www.w3.org/2005/Atom" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <title>DSpace Collection:</title>
  <link rel="alternate" href="https://ria.asturias.es/RIA/handle/123456789/6368" />
  <subtitle />
  <id>https://ria.asturias.es/RIA/handle/123456789/6368</id>
  <updated>2025-12-21T10:06:11Z</updated>
  <dc:date>2025-12-21T10:06:11Z</dc:date>
  <entry>
    <title>Zinc‐Catalyzed Synthesis of Conjugated Dienoates through Unusual Cross‐Couplings of Zinc Carbenes with Diazo Compounds</title>
    <link rel="alternate" href="https://ria.asturias.es/RIA/handle/123456789/10445" />
    <author>
      <name>Mata García, Sergio</name>
    </author>
    <author>
      <name>Vicente Arroyo, Rubén</name>
    </author>
    <author>
      <name>López García, Luis Ángel</name>
    </author>
    <author>
      <name>Gonzalez Rodríguez, Maria José</name>
    </author>
    <author>
      <name>González Martínez, Jesús</name>
    </author>
    <id>https://ria.asturias.es/RIA/handle/123456789/10445</id>
    <updated>2018-06-27T06:41:14Z</updated>
    <published>2016-11-30T00:00:00Z</published>
    <summary type="text">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.</summary>
    <dc:date>2016-11-30T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Zinc-Catalyzed Synthesis of Allylsilanes via Si–H Bond Insertion of Vinyl Carbenoids Generated from Cyclopropenes</title>
    <link rel="alternate" href="https://ria.asturias.es/RIA/handle/123456789/10447" />
    <author>
      <name>Mata García, Sergio</name>
    </author>
    <author>
      <name>Vicente Arroyo, Rubén</name>
    </author>
    <author>
      <name>López García, Luis Ángel</name>
    </author>
    <id>https://ria.asturias.es/RIA/handle/123456789/10447</id>
    <updated>2018-11-06T16:13:39Z</updated>
    <published>2017-05-10T00:00:00Z</published>
    <summary type="text">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.</summary>
    <dc:date>2017-05-10T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Zinc-Catalyzed Multicomponent Reactions: Easy Access to Furyl- Substituted Cyclopropane and 1,2-Dioxolane Derivatives</title>
    <link rel="alternate" href="https://ria.asturias.es/RIA/handle/123456789/8188" />
    <author>
      <name>López García, Luis Ángel</name>
    </author>
    <author>
      <name>Vicente Arroyo, Rubén</name>
    </author>
    <author>
      <name>González, Jesús</name>
    </author>
    <id>https://ria.asturias.es/RIA/handle/123456789/8188</id>
    <updated>2018-04-20T11:35:54Z</updated>
    <published>2016-04-27T00:00:00Z</published>
    <summary type="text">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.</summary>
    <dc:date>2016-04-27T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Zinc-catalyzed multicomponent reactions:  Straightforward synthesis of functionalized furan derivatives</title>
    <link rel="alternate" href="https://ria.asturias.es/RIA/handle/123456789/8185" />
    <author>
      <name>Mata García, Sergio</name>
    </author>
    <author>
      <name>López García, Luis Ángel</name>
    </author>
    <author>
      <name>Vicente Arroyo, Rubén</name>
    </author>
    <id>https://ria.asturias.es/RIA/handle/123456789/8185</id>
    <updated>2018-04-20T11:35:42Z</updated>
    <published>2016-06-27T00:00:00Z</published>
    <summary type="text">Title: Zinc-catalyzed multicomponent reactions:  Straightforward synthesis of functionalized furan derivatives
Authors: Mata García, Sergio; López García, Luis Ángel; Vicente Arroyo, Rubén
Abstract: A sequence consisting of an initial zinc-catalyzed Knoevenagel condensation of and forms enynone. Then a 5-exo-dig cyclization takes place to give rise to 2-furyl-zinc carbene intermediate. A final cyclopropanation reaction or insertion into the Si-H bond would account for the formation of the final products
Description: En el póster se describe la generación de ciclopropilfuranos y sililfuranos mediante metodologías multicomponente.</summary>
    <dc:date>2016-06-27T00:00:00Z</dc:date>
  </entry>
</feed>

