Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Anisley Suárez"'
Autor:
Carlos de la Cruz, Roberto Sanz, Anisley Suárez, Edgar Ventosa, Rebeca Marcilla, Andreas Mavrandonakis
Publikováno v:
ChemSusChem. 16
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::244140b98c2084ed7b89ccaa18152899
https://doi.org/10.1002/cssc.202201984
https://doi.org/10.1002/cssc.202201984
Publikováno v:
Repositorio Institucional de la Universidad de Burgos (RIUBU)
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Propargylic glycols, 2-alkynyl-1-(indol-3-yl)-1,2-diols, react with thiols undergoing a complex but selective gold-catalyzed transformation that gives rise to α-indol-3-yl α-((Z)-2-thioalkenyl) ketones. The sequence is triggered by the regioselecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae5894e6aa7470b93008e2b29bd34531
http://hdl.handle.net/10259/6090
http://hdl.handle.net/10259/6090
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fe41e9443898be4dccb16c5b0134faa7
https://pubmed.ncbi.nlm.nih.gov/33928778
https://pubmed.ncbi.nlm.nih.gov/33928778
Autor:
Noelia Velasco, Anisley Suárez, Roberto Sanz, Fernando Martínez-Lara, Samuel Suárez-Pantiga, Manuel A. Fernández-Rodríguez
Publikováno v:
Repositorio Institucional de la Universidad de Burgos (RIUBU)
instname
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This work describes the 6-endo-dig cyclization of Saryl propargyl sulfides to afford 2H-thiochromenes. The substitution at the propargylic position plays a crucial role in allowing intramolecular silver-catalyzed alkyne hydroarylation and Niodosuccin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7443a9db4cd939e7710c88a05d4783d1
http://hdl.handle.net/10259/6093
http://hdl.handle.net/10259/6093
Publikováno v:
Repositorio Institucional de la Universidad de Burgos (RIUBU)
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A straightforward and efficient synthesis of the two less explored types of indolocarbazoles has been developed. Two different processes for the carbazole nucleus preparation, a gold-catalysed regioselective cyclization followed by the dioxomolybdenu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d8fbda160dc37bd875eb05c1b932dc4
http://hdl.handle.net/10259/5401
http://hdl.handle.net/10259/5401
Publikováno v:
Repositorio Institucional de la Universidad de Burgos (RIUBU)
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An efficient methodology for the synthesis of a series of new fused polyclyclic indoles has been developed by Brønsted acidcatalyzed intramolecular Friedel−Crafts reactions of properly designed indolyl alcohols.
Ministerio de Economiá y Com
Ministerio de Economiá y Com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6f7d437343ae20bb2955dca23ecb2c7
https://doi.org/10.1021/acs.joc.5b02048
https://doi.org/10.1021/acs.joc.5b02048
Publikováno v:
Repositorio Institucional de la Universidad de Burgos (RIUBU)
instname
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Gold(III)-catalyzed cycloisomerization of α-bis(indol-3-yl)methyl alkynols selectively affords 1-(indol-3-yl)carbazoles, in a transformation that takes place through a selective 1,2-alkyl vs 1,2-vinyl migration step in the vinyl-gold intermediate ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b513b4c4fd6192438d9767cf1b67a242
http://hdl.handle.net/10259/4926
http://hdl.handle.net/10259/4926
Publikováno v:
Repositorio Institucional de la Universidad de Burgos (RIUBU)
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A convenient procedure for accessing a,a-bis(indol-3-yl) ketones from indoles and a-oxoaldehydes is described using an inexpensive and commercially available catalyst such as ptoluenesulfonic acid monohydrate. This protocol allows for the first time
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eccf56c91074c1410653b1e947a05116
http://hdl.handle.net/10259/4529
http://hdl.handle.net/10259/4529
Publikováno v:
Repositorio Institucional de la Universidad de Burgos (RIUBU)
instname
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A new and efficient synthesis of α-functionalized α-indol-3-yl ketones from easily available indolyl α-acyloins is reported. This process, catalyzed by Brønsted or Lewis acids, involves an uncommon direct nucleophilic substitution reaction of a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c72a0909ca7909d88b4e17ad6679b9c
http://hdl.handle.net/10259/4288
http://hdl.handle.net/10259/4288
Publikováno v:
Organicbiomolecular chemistry. 14(47)
A new and efficient synthesis of α-functionalized α-indol-3-yl ketones from easily available indolyl α-acyloins is reported. This process, catalyzed by Brønsted or Lewis acids, involves an uncommon direct nucleophilic substitution reaction of a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d69d548f0dc6af9564a5f8b35a8d3d2e
https://pubmed.ncbi.nlm.nih.gov/27841890
https://pubmed.ncbi.nlm.nih.gov/27841890