Zobrazeno 1 - 10
of 144
pro vyhledávání: '"Joaquín García-Álvarez"'
Autor:
María Jesús Rodríguez-Álvarez, Nicolás Ríos-Lombardía, Sergio E. García-Garrido, Carmen Concellón, Vicente del Amo, Vito Capriati, Joaquín García-Álvarez
Publikováno v:
Molecules, Vol 29, Iss 7, p 1422 (2024)
This mini-review offers a comprehensive overview of the advancements made over the last three years in utilizing highly polar s-block organometallic reagents (specifically, RLi, RNa and RMgX compounds) in organic synthesis run under bench-type reacti
Externí odkaz:
https://doaj.org/article/86f4e7168c3a47a69cfb158491d20a60
Autor:
Andrea Francesca Quivelli, Federico Vittorio Rossi, Chiara Alario, Francesco Sannicolò, Paola Vitale, Joaquín García-Álvarez, Filippo Maria Perna, Vito Capriati
Publikováno v:
Molecules, Vol 27, Iss 21, p 7594 (2022)
Dimethindene is a selective histamine H1 antagonist and is commercially available as a racemate. Upon analyzing the synthetic pathways currently available for the industrial preparation of dimethindene, we set up a sustainable approach for the synthe
Externí odkaz:
https://doaj.org/article/dd23def2d19e4a60ad8dedebc060825b
Autor:
Nicolás Ríos-Lombardía, María Jesús Rodríguez-Álvarez, Francisco Morís, Robert Kourist, Natalia Comino, Fernando López-Gallego, Javier González-Sabín, Joaquín García-Álvarez
Publikováno v:
Frontiers in Chemistry, Vol 8 (2020)
The self-assembly of styrene-type olefins into the corresponding stilbenes was conveniently performed in the Deep Eutectic Solvent (DES) mixture 1ChCl/2Gly under air and in the absence of hazardous organic co-solvents using a one-pot chemo-biocatalyt
Externí odkaz:
https://doaj.org/article/f07ef966cc9f4e14a4a38a9237ac276c
Autor:
Noel Nebra, Joaquín García-Álvarez
Publikováno v:
Molecules, Vol 25, Iss 9, p 2015 (2020)
This mini-review presents a general overview of the progress achieved during the last decade on the amalgamation of CuAAC processes (copper-catalyzed azide-alkyne cycloaddition) with the employment of sustainable solvents as reaction media. In most o
Externí odkaz:
https://doaj.org/article/f3cb56175d6948d3a9dea395fe98139c
Autor:
Joaquín García-Álvarez
Publikováno v:
Molecules, Vol 25, Iss 7, p 1493 (2020)
The use of enzymes, organo-catalysts or transition metal catalysts, as opposed to the employment of stoichiometric quantities of other traditional promoters of different organic synthetic processes (like, inorganic/organic bases, Brønsted acids, rad
Externí odkaz:
https://doaj.org/article/7d6be5eaa90449f1a911a09c3279249e
Publikováno v:
Molecules, Vol 21, Iss 11, p 1527 (2016)
To overcome the well-established drawbacks of conventional organic solvents (toxicity, non-biodegradability, flammability, accumulation in the atmosphere) remarkable research efforts have been recently devoted to the replacement of traditional organi
Externí odkaz:
https://doaj.org/article/ccefca3e83394c0c9258b33b19192439
Autor:
Davide Arnodo, Marina Ramos-Martín, Luciana Cicco, Vito Capriati, Nicolás Ríos-Lombardía, Javier González-Sabín, Alejandro Presa Soto, Joaquín García-Álvarez
Publikováno v:
Organic & Biomolecular Chemistry. 21:4414-4421
The design of a hybrid one-pot tandem protocol through the combination of biodeoximations (promoted by laccase from Trametes versicolor) and s-block polar organometallics (RLi/RMgX) in aqueous media, at room temperature and under air is reported.
Publikováno v:
Palabras preliminares ISBN: 9788413117324
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e47d88512efb7f8e1490c7ca1a91849c
https://doi.org/10.14201/0bcl0111235
https://doi.org/10.14201/0bcl0111235
Autor:
Andrea Francesca Quivelli, Federico Vittorio Rossi, Paola Vitale, Joaquín García-Álvarez, Filippo Maria Perna, Vito Capriati
Publikováno v:
ACS Sustainable Chemistry & Engineering. 10:4065-4072
Autor:
Antonio Antiñolo, Joaquín García-Álvarez, FERNANDO CARRILLO-HERMOSILLA, Blanca Parra Cadenas, David Elorriaga
Publikováno v:
Green Chemistry. 24:800-812
Addition of lithium amides (LiNR2) to carbodiimides/nitriles was achieved in sustainable solvents, under air, allowing the synthesis of guanidines/amidines.