Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Samuel Suárez‐Pantiga"'
Autor:
Claudia Feberero, Cintia Virumbrales, Carlos Sedano, Lorena Renedo, Samuel Suárez-Pantiga, Roberto Sanz
Publikováno v:
Molecules, Vol 27, Iss 2, p 525 (2022)
A straightforward and transition metal-free one-pot protocol to synthesize halobenzo[b]furans has been developed employing simple and easily available starting materials such as O-aryl carbamates and alkynylsulfones. The fine-tuning of the different
Externí odkaz:
https://doaj.org/article/10300b781b234bdf8d806e1be3b2f803
Autor:
Sara Gómez-Gil, Rubén Rubio-Presa, Raquel Hernández-Ruiz, Samuel Suárez-Pantiga, María R. Pedrosa, Roberto Sanz
Publikováno v:
Organic & Biomolecular Chemistry. 21:4185-4190
The synthesis of 1,4-dicarbonyls has been accomplished by a dioxomolybdenum-catalyzed oxidative C–C bond cleavage of cyclobutane-1,2-diols with DMSO.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::923153607009f45510897d4cf7867cef
https://doi.org/10.1039/d3ob00436h
https://doi.org/10.1039/d3ob00436h
Autor:
Miguel A. Muñoz‐Torres, Fernando Martínez‐Lara, Marta Solas, Samuel Suárez‐Pantiga, Roberto Sanz
Publikováno v:
Advanced Synthesis & Catalysis. 364:3716-3724
The combination of organolithium chemistry with gold catalysis has enabled the development of a synthetic strategy for accessing polysubstituted indoles and carbazoles from readily available starting materials. This method is based on a “back-to-fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fecfb027ef657872fb9bab0c7dfcab5
https://doi.org/10.1002/adsc.202200824
https://doi.org/10.1002/adsc.202200824
Autor:
Cintia, Virumbrales, Mahmoud A E A A A, El-Remaily, Samuel, Suárez-Pantiga, Manuel A, Fernández-Rodríguez, Félix, Rodríguez, Roberto, Sanz
Publikováno v:
Organic letters. 24(43)
A gold(I)-catalyzed cascade reaction for the stereoselective synthesis of sulfur- or selenium-containing indeno[1,2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7b4313f6766729563fd785d7c573a5bc
https://pubmed.ncbi.nlm.nih.gov/36279586
https://pubmed.ncbi.nlm.nih.gov/36279586
Autor:
Cintia Virumbrales, Mahmoud A. E. A. A. A. El-Remaily, Samuel Suárez-Pantiga, Manuel A. Fernández-Rodríguez, Félix Rodríguez, Roberto Sanz
Publikováno v:
Scopus
A gold(I)-catalyzed cascade reaction for the stereoselective synthesis of sulfur- or selenium-containing indeno[1,2-b]chromene derivatives from o-(alkynyl)styrenes substituted at the triple bond with a thio- or seleno-aryl group is described. The rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85d1fa5fdb6bacafbb03a85b8a46505c
http://hdl.handle.net/10259/7405
http://hdl.handle.net/10259/7405
Autor:
Rubén Rubio-Presa, M. José Tapia, Roberto Sanz, Samuel Suárez-Pantiga, María R. Pedrosa, Raquel Hernández-Ruiz, Manuel A. Fernández-Rodríguez
Publikováno v:
Repositorio Institucional de la Universidad de Burgos (RIUBU)
instname
Chemistry (Weinheim an Der Bergstrasse, Germany)
instname
Chemistry (Weinheim an Der Bergstrasse, Germany)
A catalytic domino reduction–imine formation–intramolecular cyclization–oxidation for the general synthesis of a wide variety of biologically relevant N‐polyheterocycles, such as quinoxaline‐ and quinoline‐fused derivatives, and phenanthr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9b0483cd0408bf44d389cdde770f5e7
https://doi.org/10.1002/chem.202102000
https://doi.org/10.1002/chem.202102000
Autor:
Martin Simon, Christopher Golz, Xaiza Aniban, Samuel Suárez-Pantiga, Manuel Alcarazo, Ricardo A. Mata, Pablo Redero
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
A series of expanded helicenes of different sizes and shapes incorporating phenyl‐ and biphenyl‐substituents at the deepest part of their fjord have been synthesized via sequential Au‐catalyzed hydroarylation of appropriately designed diynes, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2aed52717142954d3423a0f8c95eb6a
https://doi.org/10.1002/chem.202102585
https://doi.org/10.1002/chem.202102585
Publikováno v:
Angewandte Chemie. 134
The asymmetric synthesis of cyclopentachromenones from gold-catalyzed reaction of readily available skipped alkenynones is described. This cascade reaction involves an initial anti-Michael hydroarylation of the ynone moiety to form a gold-functionali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44198e3d8c28efe698c72a459f965ce8
https://doi.org/10.1002/ange.202207406
https://doi.org/10.1002/ange.202207406
Autor:
Noelia Velasco, Clara Martínez‐Núñez, Manuel A. Fernández‐Rodríguez, Roberto Sanz, Samuel Suárez‐Pantiga
A tandem 1,3-sulfur migration followed by iodocyclization reaction of propargylic sulfides in the presence of NIS in HFIP has been developed to synthesize indene-based β-iodoalkenyl sulfides. The choice of the reaction media is crucial to promote th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::077cdafd95350e20069b80949108d0fa
http://hdl.handle.net/10259/7413
http://hdl.handle.net/10259/7413
Publikováno v:
Repositorio Institucional de la Universidad de Burgos (RIUBU)
instname
instname
α-Oxy ketones, easily accessible by conventional routes, can be selectively deprotonated generating an enolate intermediate, which upon treatment with paraformaldehyde undergoes an aldol–Tishchenko reaction, leading to relevant 1,2,3-triol fragmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eafbfabd038acb9f68828cbc3aba7de8
https://doi.org/10.1055/a-1509-5655
https://doi.org/10.1055/a-1509-5655