Zobrazeno 1 - 10
of 289
pro vyhledávání: '"Víctor S. Martín"'
Publikováno v:
Arabian Journal of Chemistry, Vol 12, Iss 8, Pp 3764-3775 (2019)
The first total synthesis of the bioactive natural product 2,6-(E,E)-thymifodioic acid, also called incanic acid, and its stereoisomers is described. An unified, iterative and modular strategy was envisioned, achieving the synthesis of the goals prod
Externí odkaz:
https://doaj.org/article/06fe87c77c1a4dd889768740d9f9b37d
Autor:
Marleen Häring, Sujay Kumar Nandi, Julio Rodríguez-López, Debasish Haldar, Víctor S. Martín, Antonio Diego Lozano-Gorrín, César Saldías, David Díaz Díaz
Publikováno v:
ACS Omega, Vol 4, Iss 1, Pp 2111-2117 (2019)
Externí odkaz:
https://doaj.org/article/383f702be1854207ac5740eabacf50df
Autor:
Alberto J. Martín-Rodríguez, Sergio J. Álvarez-Méndez, Caroline Overå, Kartik Baruah, Tânia Margarida Lourenço, Parisa Norouzitallab, Peter Bossier, Víctor S. Martín, José J. Fernández
Publikováno v:
Frontiers in Cellular and Infection Microbiology, Vol 8 (2018)
Vibrio campbellii is a major pathogen in aquaculture. It is a causative agent of the so-called “luminescent vibriosis,” a life-threatening condition caused by bioluminescent Vibrio spp. that often involves mass mortality of farmed shrimps. The em
Externí odkaz:
https://doaj.org/article/d304fdfd79f3453d88b617dbb710f3dc
Autor:
Diego M. Monzón, Juan Manuel Betancort, Tomás Martín, Miguel Ángel Ramírez, Víctor S. Martín, David Díaz Díaz
Publikováno v:
Molecules, Vol 26, Iss 6, p 1629 (2021)
Cyclic products can be obtained through the intramolecular version of the Nicholas reaction, which requires having the nucleophile connected to the alkyne unit. Here, we report the synthesis of 1-oxa-3-cyclooctynes starting from commercially availabl
Externí odkaz:
https://doaj.org/article/5f010e2825364fe999afab0ba9153b32
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 957-962 (2016)
An improved protocol for the synthesis of enantiomerically pure allylic amines is reported. N-Protected α-amino esters derived from natural amino acids were submitted to a one-pot tandem reduction–olefination process. The sequential reduction with
Externí odkaz:
https://doaj.org/article/abafee33a5ea4151b90b7deea3f36a2b
Autor:
Alberto J. Martín-Rodríguez, Fernando Reyes, Jesús Martín, Juan Pérez-Yépez, Milagros León-Barrios, Alan Couttolenc, César Espinoza, Ángel Trigos, Víctor S. Martín, Manuel Norte, José J. Fernández
Publikováno v:
Marine Drugs, Vol 12, Iss 11, Pp 5503-5526 (2014)
In our search for quorum-sensing (QS) disrupting molecules, 75 fungal isolates were recovered from reef organisms (endophytes), saline lakes and mangrove rhizosphere. Their QS inhibitory activity was evaluated in Chromobacterium violaceum CVO26. Four
Externí odkaz:
https://doaj.org/article/1b3e13561fc04735904670aa6455a514
Autor:
María F. Beer, Augusto E. Bivona, Andrés Sánchez Alberti, Natacha Cerny, Guillermo F. Reta, Víctor S. Martín, José M. Padrón, Emilio L. Malchiodi, Valeria P. Sülsen, Osvaldo J. Donadel
Publikováno v:
Molecules, Vol 24, Iss 6, p 1113 (2019)
Cancer is one of the most important causes of death worldwide. Solid tumors represent the great majority of cancers (>90%) and the chemotherapeutic agents used for their treatment are still characterized by variable efficacy and toxicity. Sesquiterpe
Externí odkaz:
https://doaj.org/article/939a3a209579448d8fbbc0b84cbbd42a
Autor:
Pedro. O. Miranda, Rubén M. Carballo, Miguel A. Ramírez, Víctor S. Martín, and Juan I. Padrón
Publikováno v:
ARKIVOC, Vol 2007, Iss 4, Pp 331-343 (2006)
Externí odkaz:
https://doaj.org/article/84f2f75cb35b4f109e48545d9709f04d
Autor:
Carlos R. Carreras, Celina E. García, Víctor S. Martín, Carlos E. Tonn, David Díaz Díaz, Juan Pedro Ceñal
Publikováno v:
Molbank, Vol 2010, Iss 2, p M676 (2010)
The synthesis of (E)-2-((4R,5R)-5-((benzyloxy)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)but-2-ene-1,4-diol by a one-step reduction of the appropriate 2-substituted butenolide is reported. Product characterization was carried out by IR, 1H NMR, 13C NMR,
Externí odkaz:
https://doaj.org/article/01f6849a29e54b17b09c3e88b06a4326
Autor:
Carlos R. Carreras, Celina E. García, Víctor S. Martín, Carlos E. Tonn, David Díaz Díaz, Juan Pedro Ceñal
Publikováno v:
Molbank, Vol 2010, Iss 2, p M680 (2010)
The synthesis of(–)-5-[(4R,5R)-5-(benzyloxymethyl)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyl-4,7-dihydro-1,3-dioxepine is reported. Product characterization was carried out by IR, 1H NMR, 13C NMR, MS, elemental analysis and optical rotation.
Externí odkaz:
https://doaj.org/article/4750b22749424edfba41c77a63fc1794