Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Aitor Ortega"'
Autor:
CRISTINA MORENO-CABRERIZO, AITOR ORTEGA-MARTÍNEZ, CYNTHIA MOLINA, CARMEN NÁJERA, JOSÉ M. SANSANO
Publikováno v:
Anais da Academia Brasileira de Ciências, Vol 90, Iss 1 suppl 2, Pp 1089-1099
ABSTRACT The synthesis of 3,3-disubstituted N-methyloxindoles, starting from 3-acetyl-2-hydroxy-1-methyloxindole employing a sequential one-pot synthesis, is studied. The process involves a first alkylation in the presence of 1 equiv. of both organic
Externí odkaz:
https://doaj.org/article/ac0a3d3de0e5452e95868e89d8491cc0
Autor:
Patel, Arun, Albaladejo, Miguel Martinez, Puchades, Vicente Puchades, Amores, David Ramos, Arteaga, Jonathan Suárez, González, Aitor Ortega, Berna, Alfredo Serna
Publikováno v:
In Radiotherapy and Oncology May 2024 194 Supplement 1:S4770-S4773
Autor:
Cristina Moreno-Cabrerizo, José M. Sansano, Aitor Ortega-Martínez, Miguel A. Esteruelas, Ana M. López, Carmen Nájera
Publikováno v:
European Journal of Organic Chemistry. 2020:3101-3109
We gratefully acknowledge financial support from the Spanish Ministerio de Ciencia, Innovacion y Universidades (projects CTQ2016-81893REDT, and RED2018-102387-T) the Spanish Ministerio de Economia, Industria y Competitividad, Agencia Estatal de Inves
Autor:
Belén Vaz, Francisco Cruz, Youssef Madich, Rosana Alvarez, Jose M. Aurrecoechea, Aitor Ortega, Unai Vilar
Publikováno v:
Organometallics. 37:3813-3826
A regioselective heterocyclization–Sonogashira coupling cascade between 2-alkynylbenzamides and terminal alkynes is described. The reaction proceeds under Pd(II) catalysis, with air used as a terminal oxidant to regenerate the catalyst from the Pd(
Autor:
Cynthia Molina, Cristina Moreno-Cabrerizo, José M. Sansano, Carmen Nájera, Aitor Ortega-Martínez
Publikováno v:
European Journal of Organic Chemistry. 2018:2394-2405
We gratefully acknowledge financial support from the Spanish Ministerio de Economia y Competitividad (MINECO) (projects CTQ2013-43446-P and CTQ2014-51912-REDC), the Spanish Ministerio de Economia, Industria y Competitividad, Agencia Estatal de Invest
Publikováno v:
RUA. Repositorio Institucional de la Universidad de Alicante
Universidad de Alicante (UA)
Universidad de Alicante (UA)
The Pd-catalyzed allylation of 3-acetyl-2-oxindoles with allyl alcohol is performed using 3 mol% of Pd(dba)2, rac-BINAP and BINOL phosphoric acid as catalytic mixture. This procedure allows the in situ synthesis of 3-allyl-2-oxindole by adding Triton
Autor:
Fabio Calcinelli, Daniele Mazzarella, Filippo Monti, Andrea Gualandi, Luca Mengozzi, Aitor Ortega-Martínez, Pier Giorgio Cozzi, Nicola Armaroli, Letizia Sambri, Elia Matteucci
Publikováno v:
Alma Mater Studiorum Università di Bologna-IRIS
ACS catalysis 7 (2017): 5357–5362. doi:10.1021/acscatal.7b01669
info:cnr-pdr/source/autori:Gualandi, Andrea; Mazzarella, Daniele; Ortega-Martinez, Aitor; Mengozzi, Luca; Calcinelli, Fabio; Matteucci, Elia; Monti, Filippo; Armaroli, Nicola; Sambri, Letizia; Cozzi, Pier Giorgio/titolo:Photocatalytic Radical Alkylation of Electrophilic Olefins by Benzylic and Alkylic Zinc-Sulfinates/doi:10.1021%2Facscatal.7b01669/rivista:ACS catalysis/anno:2017/pagina_da:5357/pagina_a:5362/intervallo_pagine:5357–5362/volume:7
ACS catalysis 7 (2017): 5357–5362. doi:10.1021/acscatal.7b01669
info:cnr-pdr/source/autori:Gualandi, Andrea; Mazzarella, Daniele; Ortega-Martinez, Aitor; Mengozzi, Luca; Calcinelli, Fabio; Matteucci, Elia; Monti, Filippo; Armaroli, Nicola; Sambri, Letizia; Cozzi, Pier Giorgio/titolo:Photocatalytic Radical Alkylation of Electrophilic Olefins by Benzylic and Alkylic Zinc-Sulfinates/doi:10.1021%2Facscatal.7b01669/rivista:ACS catalysis/anno:2017/pagina_da:5357/pagina_a:5362/intervallo_pagine:5357–5362/volume:7
The decarboxylative coupling of carboxylic acids has numerous applications in photoredox catalysis.(1) In these reactions, monoelectronic oxidation of carboxylate anions, followed by carbon dioxide evolution from the so formed RCOO•, gave entry to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e679fc23dbd35f7de52ab4a36e845138
http://hdl.handle.net/11585/622683
http://hdl.handle.net/11585/622683
Publikováno v:
Organicbiomolecular chemistry. 17(3)
The fluorination of 3-acetyl-2-oxindoles with N-fluorobenzenesulfonimide under Lewis acid catalysis using Mg(ClO4)2 gives the starting compounds 3-acetyl-3-fluoro-2-oxindoles. These compounds are subjected to base-promoted deacylative alkylation (DaA
Autor:
Aitor Ortega-Martínez, Cristina Moreno-Cabrerizo, Cynthia Molina, Carmen Nájera, José M. Sansano
Publikováno v:
RUA. Repositorio Institucional de la Universidad de Alicante
Universidad de Alicante (UA)
Anais da Academia Brasileira de Ciências, Vol 90, Iss 1 suppl 2, Pp 1089-1099
Anais da Academia Brasileira de Ciências, Volume: 90, Issue: 1 Supplement 2, Pages: 1089-1099, Published: 2018
Anais da Academia Brasileira de Ciências v.90 n.1 suppl.2 2018
Anais da Academia Brasileira de Ciências
Academia Brasileira de Ciências (ABC)
instacron:ABC
Universidad de Alicante (UA)
Anais da Academia Brasileira de Ciências, Vol 90, Iss 1 suppl 2, Pp 1089-1099
Anais da Academia Brasileira de Ciências, Volume: 90, Issue: 1 Supplement 2, Pages: 1089-1099, Published: 2018
Anais da Academia Brasileira de Ciências v.90 n.1 suppl.2 2018
Anais da Academia Brasileira de Ciências
Academia Brasileira de Ciências (ABC)
instacron:ABC
The synthesis of 3,3-disubstituted N-methyloxindoles, starting from 3-acetyl-2-hydroxy-1-methyloxindole employing a sequential one-pot synthesis, is studied. The process involves a first alkylation in the presence of 1 equiv. of both organic halide a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1256f2de953adf9ea728055901e4dcda
http://hdl.handle.net/10045/76371
http://hdl.handle.net/10045/76371
Autor:
Larbi Belachemi, Rosana Alvarez, Youssef Madich, Angel R. de Lera, Jose M. Aurrecoechea, Aitor Ortega, J. Gabriel Denis, Abdellatif Matrane, Claudio Martínez
Publikováno v:
Synthesis. 45:2009-2017
A three-component, one-pot, stepwise Sonogashira–heterocyclization–Heck-coupling process was developed starting from either haloarenecarboxamides, halophenols or haloanilines, terminal alkynes and electron-deficient alkenes. Cyclic imidate-, be