Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Sara Cembellín"'
Publikováno v:
Organic Chemistry Frontiers. 10:1773-1779
An indium-promoted lactonization of (indol-3-yl)-2-oxoacetaldehydes, which allows the synthesis of substituted γ-methylenebutenolides in an aqueous environment, has been accomplished. This process is in clear contrast with the established metal-medi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c64c2ebec7f47ce7de5d4179dd179183
https://doi.org/10.1039/d3qo00133d
https://doi.org/10.1039/d3qo00133d
Autor:
Sara Cembellín
Publikováno v:
Handbook of CH‐Functionalization. :1-32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c2ea4ff814734d202875c835fe5d1c1
https://doi.org/10.1002/9783527834242.chf0228
https://doi.org/10.1002/9783527834242.chf0228
Autor:
Sara Cembellín, Iván Maisuls, Constantin G. Daniliuc, Helena Osthues, Nikos L. Doltsinis, Cristian A. Strassert, Frank Glorius
Publikováno v:
Organic & Biomolecular Chemistry. 20:796-800
A selective synthesis of relevant fluorescent compounds, indolizino[3,4,5-ab]isoindoles (INIs), through a Mn(i)-catalyzed C–H activation on readily available 2-phenylpyridines is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::426900a6c2f99ea185dff1b727451a54
https://doi.org/10.1039/d1ob02246f
https://doi.org/10.1039/d1ob02246f
Publikováno v:
ChemCatChem. 13:5156-5165
A half-sandwich ruthenium-p-cymene organometallic complex has been immobilized at Single Walled Carbon Nanotubes (SWNT) sidewalls through a stepwise covalent chemistry protocol. The introduction of amino groups by means of diazonium-chemistry protoco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::453e6e373104cc44c63bdeff30abbba6
https://doi.org/10.1002/cctc.202101442
https://doi.org/10.1002/cctc.202101442
Autor:
Sara Cembellín, Belen Batanero
Publikováno v:
The Chemical Record. 21:2453-2471
The adoption of new measures that preserve our environment, on which our survival depends, is a necessity. Electro-organic processes are sustainable per se, by producing the activation of a substrate by electron transfer at normal pressure and room t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30edf72dee40c3b4fa72f4a6ce033ea2
https://doi.org/10.1002/tcr.202100128
https://doi.org/10.1002/tcr.202100128
Autor:
Sara, Cembellín, Iván, Maisuls, Constantin G, Daniliuc, Helena, Osthues, Nikos L, Doltsinis, Cristian A, Strassert, Frank, Glorius
Publikováno v:
Organicbiomolecular chemistry. 20(4)
Herein, a regioselective synthesis of indolizino[3,4,5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::83e8655699e5f5125842b1d6fd11fd89
https://pubmed.ncbi.nlm.nih.gov/35006235
https://pubmed.ncbi.nlm.nih.gov/35006235
Publikováno v:
ACS Catalysis. 10:197-202
A highly selective Mn(I)-catalyzed alkenylation of arenes and heteroarenes with 1,3-diynes is described. The reported transformation overcomes regio-, chemo-, and stereoselectivity challenges assoc...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1847a22587cb55ed8d3430aa103a9942
https://doi.org/10.1021/acscatal.9b03965
https://doi.org/10.1021/acscatal.9b03965
Publikováno v:
Chemical Science
Herein we describe an unprecedented RuII-catalyzed site-selective and regiospecific annulation of benzoic acids with propargylic carbonates. The weakly coordinating carboxylic acid moiety outperformed other typically used directing groups in C–H ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::474e0cf5c9df97f57775fba35c59f2a4
https://doi.org/10.1039/c9sc01703h
https://doi.org/10.1039/c9sc01703h
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:
Angewandte Chemie International Edition. 57:10732-10736
An unprecedented MnI /AgI -relay-catalyzed C(sp2 )-H/C(sp3 )-H coupling of (vinyl)arenes with α-diazoketones is reported, wherein the diazo group was exploited as a traceless auxiliary for control of regioselectivity. Challenging β-(hetero)aryl/alk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::062a695e781bcc0df25dc27c9fb4bd0a
https://doi.org/10.1002/anie.201803384
https://doi.org/10.1002/anie.201803384