Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Javier Luis‐Barrera"'
Autor:
Ana María Martínez-Gualda, Rafael Cano, Leyre Marzo, Raúl Pérez-Ruiz, Javier Luis-Barrera, Rubén Mas-Ballesté, Alberto Fraile, Víctor A. de la Peña O’Shea, José Alemán
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-10 (2019)
Tsuji–Trost allylation is a traditional method for selective C-C bond formation that involves the use of palladium-based catalysts. Here, the authors report a metal-free, photocatalytic allylation of several heterocycles, amines and alcohols, which
Externí odkaz:
https://doaj.org/article/fd3d2e4fba32438aa7e7ccec9808db86
Autor:
Estefanía Capel, Javier Luis-Barrera, Ana Sorazu, Uxue Uria, Liher Prieto, Efraím Reyes, Luisa Carrillo, Jose L. Vicario
Publikováno v:
The Journal of Organic Chemistry. 87:10062-10072
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ce6e8c6bc010c3e544f2f12316c11b3
https://doi.org/10.1021/acs.joc.2c01045
https://doi.org/10.1021/acs.joc.2c01045
Autor:
Javier Luis‐Barrera, Sandra Rodriguez, Uxue Uria, Efraim Reyes, Liher Prieto, Luisa Carrillo, Manuel Pedrón, Tomás Tejero, Pedro Merino, Jose L. Vicario
Publikováno v:
Chemistry – A European Journal. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6bed947245238c09022861c5207dab5
https://doi.org/10.1002/chem.202203257
https://doi.org/10.1002/chem.202203257
Autor:
Rubén Mas-Ballesté, Alicia Jimenez-Almarza, Felipe Gándara, Daniel Maspoch, Claudia Vignatti, Javier Luis-Barrera, Inhar Imaz, Zahra Dolatkhah, Anna Broto-Ribas, José Alemán
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Biblos-e Archivo. Repositorio Institucional de la UAM
A well-established strategy to synthesize heterogeneous, metal-organic framework (MOF) catalysts that exhibit nanoconfinement effects, and specific pores with highly-localized catalytic sites, is to use organic linkers containing organocatalytic cent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ff1dee4fa186fd92db638d445fd4453
https://doi.org/10.1007/s12274-020-2779-8
https://doi.org/10.1007/s12274-020-2779-8
Autor:
Javier Luis‐Barrera, Sandra Rodriguez, Uxue Uria, Efraim Reyes, Liher Prieto, Luisa Carrillo, Manuel Pedrón, Tomás Tejero, Pedro Merino, Jose L. Vicario
We have studied the enantioselective transannular aminohalogenation reaction of unsaturated medium-sized cyclic benzosulfonamides by using both chiral Brønsted acid and phase-transfer catalysis. Under optimized conditions, a variety of bicyclic addu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd2031593302fd567e07ca998f67a48d
http://hdl.handle.net/10261/303535
http://hdl.handle.net/10261/303535
Autor:
Rubén Mas-Ballesté, Mariona Sodupe, Xavier Solans-Monfort, Francesca Peccati, José Alemán, Víctor Laina-Martín, Thomas Rigotti, Marta Liras, Javier Luis-Barrera
Publikováno v:
Angewandte Chemie International Edition
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Described herein is a new visible-light photocatalytic strategy for the synthesis of enantioenriched dihydrofurans and cyclopentenes by an intramolecular nitro cyclopropane ring expansion reaction. Mechanistic studies and DFT calculations are used to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10a5956a2ee51644d9f669f06d580420
https://doi.org/10.1002/ange.201703334
https://doi.org/10.1002/ange.201703334
Autor:
Alberto Fraile, Víctor A. de la Peña O’Shea, Rafael Cano, José Alemán, Rubén Mas-Ballesté, Javier Luis-Barrera, Leyre Marzo, Raúl Pérez-Ruiz, Ana María Martinez-Gualda
Publikováno v:
Nature Communications
Nature Communications, Vol 10, Iss 1, Pp 1-10 (2019)
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Nature Communications, Vol 10, Iss 1, Pp 1-10 (2019)
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
The most useful strategies for the alkylation of allylic systems are related to the Tsuji–Trost reaction or the use of different Lewis acids. Herein we report a photocatalytic approach for the allylation reaction of a variety of nucleophiles, such
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2aea16474cff2641241ce576bcc878bc
Autor:
Andrea Gini, Rubén Mas-Ballesté, Mercedes Zurro, Julia Bamberger, José Alemán, Olga García Mancheño, Javier Luis-Barrera
Publikováno v:
ResearcherID
A metal-free synthesis of biologically important benzazepines is achieved through a single synthetic operation involving an oxidative C–H bond functionalization and ring expansion with diazomethanes as key reagent. This represents a new, strong met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6361c55acbf3aba054e523d5fa8d2cc0
https://doi.org/10.1002/adsc.201600985
https://doi.org/10.1002/adsc.201600985
Autor:
Daniel Maspoch, Vincent Guillerm, Inhar Imaz, Rubén Mas-Ballesté, Claudia Vignatti, Javier Luis-Barrera, José Alemán
Publikováno v:
ChemCatChem
ChemCatChem, Wiley, 2018, 10 (18), pp.3995-3998. ⟨10.1002/cctc.201801127⟩
Digital.CSIC. Repositorio Institucional del CSIC
instname
Biblos-e Archivo. Repositorio Institucional de la UAM
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
ChemCatChem, Wiley, 2018, 10 (18), pp.3995-3998. ⟨10.1002/cctc.201801127⟩
Digital.CSIC. Repositorio Institucional del CSIC
instname
Biblos-e Archivo. Repositorio Institucional de la UAM
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Tandem and multicomponent one‐pot reactions are highly attractive because they enable synthesis of target molecules in a single reaction vessel. However, they are difficult to control, as they can lead to the formation of many undesired side‐prod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e33a00edc939ef2f0dcb18574be061f
http://hdl.handle.net/10261/199857
http://hdl.handle.net/10261/199857
Publikováno v:
ChemPlusChem. 80:1595-1600
Cyclopropanes with a quaternary center are efficiently synthesized starting from bromonitroalkenes and alkyl aldehydes under aminocatalysis, giving good yield, excellent enantioselectivities, and moderate to excellent diastereoselectivities. This wor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0652a2dce8d04262179dd4707d6ee3ae
https://doi.org/10.1002/cplu.201500320
https://doi.org/10.1002/cplu.201500320