Zobrazeno 1 - 10
of 77
pro vyhledávání: '"M. Belén Cid"'
Publikováno v:
Organic & Biomolecular Chemistry. 21:807-816
B2nep2 efficiently cleaves the N–O bond of nitrones through a concerted mechanism to form imines in very high yields via a simple, efficient and scalable protocol. Typical radical traps like DMPO and TEMPO are also deoxygenated by diboron reagents.
Autor:
M. Belén Cid, Cristina Díaz, Mariola Tortosa, Raquel Sainz, Al Mokhtar Lamsabhi, Mario Franco
Publikováno v:
Catalysis Science & Technology. 11:3501-3513
Carbon-supported catalysts have been considered as macromolecular ligands which modulate the activity of the metallic catalytic center. Understanding the properties and the factors that control the interactions between the metal and support allows a
Publikováno v:
Chemical Communications. 57:11653-11656
We have proven that pyridine–boryl complexes can be used as superelectron donors to promote the coupling of thiols and aromatic halides through a SRN1 mechanism. The reaction is efficient for a broad substrate scope, tolerating heterocycles includi
Autor:
Mario Franco, José Luis Aceña, Rafael Ramírez-Jiménez, Raquel Sainz, Rafael Ferritto, Eduardo Rodrigo, M. Belén Cid, Al Mokhtar Lamsabhi
Publikováno v:
Journal of Materials Chemistry A. 6:12637-12646
An unusual reaction between GO, DBU and DMF, that typically uses base and solvent, has been thoroughly analyzed providing valuable basic knowledge about the reactivity of GO, which is essential to control functionalization and therefore the propertie
Publikováno v:
The Journal of Organic Chemistry. 81:10887-10899
The easily available vinyl sulfone 3 showed great potential for new applications in several fields such as organic synthesis and bioconjugate formation. This was demonstrated by performing a systematic assessment of its reactivity in Michael, radical
Autor:
Leonardo Degennaro, Renzo Luisi, Ana González, Asier Goñi, Giuseppe Romanazzi, José Luis Aceña, Alejandro de la Esperanza, M. Belén Cid, Raquel Sainz, Sonia De Angelis, Claudia Carlucci, Alessandra Triminì, Valentina Petrelli, Mario Franco, Rafael Ferritto
The use of graphene derivatives as supports improves the properties of heterogeneous catalysts, with graphene oxide (GO) being the most frequently employed. To explore greener possibilities as well as to get some insights into the role of the differe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17a5b1ef3d748559641482ca212eeca7
http://hdl.handle.net/11589/187945
http://hdl.handle.net/11589/187945
Publikováno v:
ACS Catalysis. 6:84-91
The formation of nitrones by direct condensation between equimolecular amounts of N-substituted hydroxylamine hydrochlorides and aromatic or aliphatic aldehydes is efficiently promoted by pyrrolidine in a matter of minutes under very mild conditions
Publikováno v:
Organic letters. 20(18)
A simple method to transform sulfones into nitrones and therefore into the corresponding carbonyl derivatives has been developed. Some examples demonstrate that it is a new reliable and versatile reaction in the toolbox of sulfones that has great syn
Autor:
José Luis Aceña, José L. García Ruano, Sara Morales, Alfonso García Rubia, M. Belén Cid, Eduardo Rodrigo
Publikováno v:
Organic Syntheses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef1e2777395e58b80216631b337135bd
https://doi.org/10.1002/0471264229.os094.25
https://doi.org/10.1002/0471264229.os094.25
Autor:
Inés Alonso, Eduardo Rodrigo, José L. García Ruano, Sara Duce, Ana Poveda, Al Mokhtar Lamsabhi, Pablo Mauleón, Sara Morales, M. Belén Cid
Publikováno v:
Biblos-e Archivo: Repositorio Institucional de la UAM
Universidad Autónoma de Madrid
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Universidad Autónoma de Madrid
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
The Michael addition of activated methylenes to β-substituted α,β-unsaturated aldehydes (enals) via iminium catalysis takes place following reactivity and enantioselectivity patterns which depend on the electronic nature of the substituent in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddc7a38c4f2e8dfe6decb5120267eed7
http://hdl.handle.net/10486/681765
http://hdl.handle.net/10486/681765