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<field name="value">Muñoz Torres, Miguel Ángel</field>
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<field name="orcid_id">0000-0003-4372-9144</field>
<field name="value">Martínez Lara, Fernando</field>
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<field name="confidence">600</field>
<field name="orcid_id">0000-0002-2783-6778</field>
<field name="value">Solas Luera, Marta</field>
<field name="authority">542</field>
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<field name="orcid_id">0000-0002-0052-7270</field>
<field name="value">Suarez Pantiga, Samuel</field>
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<field name="orcid_id">0000-0002-4249-7807</field>
<field name="value">Sanz Díez, Roberto</field>
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<field name="confidence">600</field>
<field name="orcid_id">0000-0003-2830-0892</field>
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<field name="value">2023-02-07T13:34:36Z</field>
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<field name="value">2023-02-07T13:34:36Z</field>
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<field name="value">2022-09</field>
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<field name="value">1615-4150</field>
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<field name="value">http://hdl.handle.net/10259/7416</field>
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<field name="value">10.1002/adsc.202200824</field>
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<field name="value">1615-4169</field>
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<field name="value">The combination of organolithium chemistry with gold catalysis has enabled the development of a&#xd;
synthetic strategy for accessing polysubstituted indoles and carbazoles from readily available starting materials.&#xd;
This method is based on a “back-to-front” approach from ketopyrroles, generated by intramolecular&#xd;
carbolithiation of N,N-bis-(2-lithioallyl)amines that evolve into 3,4-bis(lithiomethyl)dihydropyrrole intermediates capable of reacting with carboxylic esters and Weinreb amides. These ketopyrroles have demonstrated to&#xd;
be excellent precursors of mono or bis(alkynols)pyrroles that, under gold-catalysis, experience a&#xd;
benzannulation reaction providing access to regioselectively substituted indoles or carbazoles.</field>
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<field name="value">We gratefully acknowledge Ministerio de Ciencia e Innovación MCIN/AEI/10.13039/501100011033 (PID2020-115789GBC21), and Junta de Castilla y León and FEDER (BU049P20) for financial support. The project leading to these results has received funding from “la Caixa” Foundation, under the Agreement LCF/PR/PR18/51130007> (CAIXA-UBU001). M.A.M., F.M.-L., M.S. and S.S.-P. thank Junta de Castilla y León (Consejería de Educación) and Fondo Social Europeo for predoctoral (M.A.M, F.M.-L. and M.S.) and postdoctoral (S.S.- P.) contracts, respectively.</field>
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<field name="value">eng</field>
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<field name="value">Wiley</field>
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<field name="value">Advanced Synthesis &amp; Catalysis. 2022, V. 364, n. 21, p. 3716-3724</field>
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<field name="value">info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-115789GB-C21/ES/ESTRATEGIAS SINTETICAS SOSTENIBLES PARA LA TRANSFORMACION DIRECTA DE NITROCOMPUESTOS Y DESARROLLO DE NUEVAS REACCIONES CATALIZADAS POR ORO/</field>
<field name="value">info:eu-repo/grantAgreement/Junta de Castilla y León//BU049P20//Estrategias sintéticas sostenibles para la halogenación directa de nitrocompuestos y la preparación de electrolitos orgánicos para baterías de flujo redox/</field>
<field name="value">info:eu-repo/grantAgreement/Fundación Bancaria Caixa d'Estalvis i Pensions de Barcelona//LCF%2FPR%2FPR18%2F51130007// Fluoración Directa de Nitrocompuestos y Sales de Heteroaril Fosfonio: Síntesis de Fluorocompuestos/FluNitroPhos/</field>
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<field name="value">Carbolithiation</field>
<field name="value">Gold</field>
<field name="value">Homogeneous catalysis</field>
<field name="value">Nitrogen heterocycles</field>
<field name="value">Organolithiums</field>
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<field name="value">“Back‐to‐Front” Indole and Carbazole Synthesis from N,N‐Bis‐(2‐bromoallyl)amines by Combining Carbolithiation Reactions with Gold‐Catalysis</field>
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<field name="value">Advanced Synthesis &amp; Catalysis</field>
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