Zobrazeno 1 - 10
of 70
pro vyhledávání: '"M. Carmen Maestro"'
Publikováno v:
Catalysts, Vol 10, Iss 5, p 562 (2020)
The innate electrophilicity of imine building blocks has been exploited in organic synthetic chemistry for decades. Inspired by the resurgence in photocatalysis, imine reactivity has now been redesigned through the generation of unconventional and ve
Externí odkaz:
https://doaj.org/article/dee34b23bd9c479eb059c277db9dfeb4
Autor:
Roberto del Río-Rodríguez, Lorena Fragoso-Jarillo, Alberto F. Garrido-Castro, M. Carmen Maestro, Jose A. Fernández-Salas, José Alemán
Herein, we report, a general, facile and environmentally friendly Minisci-type alkylation of N-heteroarenes under simple and straightforward electrochemical conditions using widely available alkyl halides as radical precursors. Primary, secondary and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72551f65305e2c73625ce2fb58f274be
https://doi.org/10.1039/d2sc01799g
https://doi.org/10.1039/d2sc01799g
Autor:
Roberto, Del Río-Rodríguez, Lorena, Fragoso-Jarillo, Alberto F, Garrido-Castro, M Carmen, Maestro, Jose A, Fernández-Salas, José, Alemán
Publikováno v:
Chemical science. 13(22)
Herein, we report, a general, facile and environmentally friendly Minisci-type alkylation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::119f6504a5c77b495828d00798e0678d
https://pubmed.ncbi.nlm.nih.gov/35756520
https://pubmed.ncbi.nlm.nih.gov/35756520
Autor:
Jose Julian Aleman Lara, Jose Aleman, Noelia Salaverri, Alberto F. Garrido-Castro, M. Carmen Maestro
Publikováno v:
Organic Letters
Aryl radical generation and manipulation constitutes a long-standing challenge in organic synthesis. Photocatalytic single-electron reduction of aryl halides has been established as a premier activation pathway to reach these intermediates. The curre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ce32698624e0e117c089d777391a1d9
https://doi.org/10.1021/acs.orglett.9b01911
https://doi.org/10.1021/acs.orglett.9b01911
Publikováno v:
Chemical communications (Cambridge, England). 56(26)
The current study presents a direct CF2H radical addition to C[double bond, length as m-dash]N bonds predicated on the photocatalytic activation of commercially available zinc difluoromethanesulfinate. The mild conditions in place lead to impressive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fc29de5414c98374aea40362616b6fcc
https://pubmed.ncbi.nlm.nih.gov/32129433
https://pubmed.ncbi.nlm.nih.gov/32129433
Publikováno v:
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Chemical Communications
instname
Chemical Communications
The current study presents a direct CF2H radical addition to C=N bonds predicated on the photocatalytic activation of commercially available zinc difluoromethanesulfinate. The mild conditions in place lead to impressive structural diversity, as quino
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0dec878669fb12fcf312001acebbf527
https://doi.org/10.1039/d0cc01353f
https://doi.org/10.1039/d0cc01353f
Publikováno v:
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Catalysts, Vol 10, Iss 562, p 562 (2020)
instname
Catalysts, Vol 10, Iss 562, p 562 (2020)
The innate electrophilicity of imine building blocks has been exploited in organic synthetic chemistry for decades. Inspired by the resurgence in photocatalysis, imine reactivity has now been redesigned through the generation of unconventional and ve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b546d80d25c5f29d8abf1e5e16883ce3
http://hdl.handle.net/10486/698584
http://hdl.handle.net/10486/698584
Autor:
Leyre Marzo, Mateo Berton, M. Carmen Maestro, Adnane Halima-Salem, María Jesús Cabrera-Afonso, Sara Cembellín, Abdellah Miloudi, José Alemán
Publikováno v:
Green Chemistry
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
A sustainable synthesis of isothiazoles has been developed using an α-amino-oxy acid auxiliary and applying photoredox catalysis. This simple strategy features mild conditions, broad scope and wide functional group tolerance representing a new envir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9facd8ee22e874e0da2f3ed00a1fcf2e
Publikováno v:
Tetrahedron Letters
Embargo de 24 meses desde fecha de publicación por política editorial
The state of asymmetric photocatalysis is exceptionally promising, as chemists from different fields and backgrounds have converged to solve a longstanding issue: stereocont
The state of asymmetric photocatalysis is exceptionally promising, as chemists from different fields and backgrounds have converged to solve a longstanding issue: stereocont
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50a53a2619408ba0eb0e465f1b9a9b14
https://doi.org/10.1016/j.tetlet.2018.02.040
https://doi.org/10.1016/j.tetlet.2018.02.040
Publikováno v:
The Journal of organic chemistry. 83(20)
A highly diastereoselective Refortmatsky reaction to N- tert-butanesulfinyl propargylaldimines and ketimines is presented. The reaction proceeded with excellent yields and diastereoselectivities provided by the sulfinyl group in the presence of Me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1e7ec81d618351f059bb800b5568615
https://pubmed.ncbi.nlm.nih.gov/30216719
https://pubmed.ncbi.nlm.nih.gov/30216719