Zobrazeno 1 - 10
of 102
pro vyhledávání: '"Manuel A. Fernández‐Rodríguez"'
Autor:
Ana M. Sanjuán, Alberto Martínez, Patricia García-García, Manuel A. Fernández-Rodríguez, Roberto Sanz
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 2242-2249 (2013)
The cyclization of o-(alkynyl)-3-(methylbut-2-enyl)benzenes, 1,6-enynes having a condensed aromatic ring at C3–C4 positions, has been studied under the catalysis of cationic gold(I) complexes. The selective 6-endo-dig mode of cyclization observed f
Externí odkaz:
https://doaj.org/article/903b05ebdcfc41b3b79d41b748b5c7eb
Autor:
Estela Álvarez, Delia Miguel, Patricia García-García, Manuel A. Fernández-Rodríguez, Félix Rodríguez, Roberto Sanz
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 7, Iss 1, Pp 786-793 (2011)
The selectivity of our previously described gold-catalyzed tandem reaction, 1,2-indole migration followed by aura-iso-Nazarov cyclization, of 3-propargylindoles bearing (hetero)aromatic substituents at both the propargylic and terminal positions, was
Externí odkaz:
https://doaj.org/article/282d09694b2f4fe1b5ad2a177641ca58
Autor:
Ana Milián, Patricia García‐García, Juan J. Vaquero, Roberto Sanz, Manuel A. Fernández‐Rodríguez
Publikováno v:
Advanced Synthesis & Catalysis. 364:3960-3966
Publikováno v:
Organic Letters. 24:5860-5865
Reaction of BCl
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
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
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
Autor:
Ana, Milián, Manuel A, Fernández-Rodríguez, Estíbaliz, Merino, Juan J, Vaquero, Patricia, García-García
Publikováno v:
Angewandte Chemie (International ed. in English). 61(28)
Metal-free borylative cyclization of biphenyl-embedded 1,3,5-trien-7-ynes in the presence of simple and inexpensive BCl
Autor:
Noelia, Velasco, Anisley, Suárez, Fernando, Martínez-Lara, Manuel Ángel, Fernández-Rodríguez, Roberto, Sanz, Samuel, Suárez-Pantiga
Publikováno v:
The Journal of Organic Chemistry
This work describes the 6-endo-dig cyclization of S-aryl propargyl sulfides to afford 2H-thiochromenes. The substitution at the propargylic position plays a crucial role in allowing intramolecular silver-catalyzed alkyne hydroarylation and N-iodosucc