<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-17T06:18:16Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:10256/25120" metadataPrefix="marc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:10256/25120</identifier><datestamp>2024-10-29T23:15:25Z</datestamp><setSpec>com_2072_452955</setSpec><setSpec>com_2072_2054</setSpec><setSpec>col_2072_453073</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Díaz Jiménez, Àlex</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Roglans i Ribas, Anna</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Solà i Puig, Miquel</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Pla i Quintana, Anna</subfield>
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      <subfield code="c">2024-07-07</subfield>
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      <subfield code="a">The continued progress in creating novel acceptorless dehydrogenations for environmentally friendly and efficient chemical synthesis is anticipated to be significantly shaped by the design of efficient catalysts that can do the job. In this study, we present a comprehensive mechanistic investigation utilizing DFT calculations to elucidate the mechanism of the [RhCl(PPh3)3]-catalysed dehydrogenative cycloaddition of cyano-yne-allene substrates. Overall, the reaction can be described as a cycloaddition involving the three unsaturations, followed by a hydrogen shift, 6π electrocyclization and acceptorless H2 elimination. The crucial factors contributing to the observed reactivity are as follows: (i) the favoured cycloaddition pathway involves the external double bond of the allene in the formation of the initial metallacycle; (ii) the stabilization of the alkyne insertion intermediate that occurs through η3-coordination to the rhodium; and (iii) the presence of a weak base that assists in deprotonation</subfield>
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      <subfield code="a">We are grateful for the financial support from the Ministerio de Ciencia, Innovación y Universidades (Projects PID2020-113711GB-I00 MCIN/AEI/10.13039/50110001103, RED2022-134074-T, RED2022-134331-T, and predoctoral fellowship FPU18/02912 to A. D.-J.) and the Generalitat de Catalunya (Project 2021-SGR-623)</subfield>
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   <datafield ind2=" " ind1=" " tag="520">
      <subfield code="a">Open Access funding provided thanks to the CSUC agreement with Royal Society of Chemistry (RSC)</subfield>
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      <subfield code="a">http://hdl.handle.net/10256/25120</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">Reaccions d'addició</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">Addition reactions</subfield>
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      <subfield code="a">Catàlisi</subfield>
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      <subfield code="a">Catalysis</subfield>
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      <subfield code="a">Catalitzadors de rodi</subfield>
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      <subfield code="a">Rhodium catalyst</subfield>
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      <subfield code="a">Rodi</subfield>
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      <subfield code="a">Rhodium</subfield>
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      <subfield code="a">Ciclització (Química)</subfield>
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      <subfield code="a">Ring formation (Chemistry)</subfield>
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      <subfield code="a">Mechanistic insights into the rhodium catalysed dehydrogenative cycloaddition of cyano-yne-allene substrates</subfield>
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