Zobrazeno 1 - 10
of 348
pro vyhledávání: '"Pedro, Almendros"'
Autor:
José M. Alonso, Pedro Almendros
Publikováno v:
Advanced Synthesis & Catalysis. 365:1332-1384
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
Autor:
José Marco-Contelles, Daniel Diez-Iriepa, Mireia Toledano-Pinedo, Alicia Porro, Pedro Almendros, M. Mercedes Rodríguez-Fernández, Abdelouahid Samadi, Isabel Iriepa, Francisco López-Muñoz, Aizpea Artetxe-Zurutuza, Ander Matheu
The present work describes the design, and synthesis of the polyfunctionalized indole derivative Contilistat for the treatment of a broad diversity of cancers, and neurodegenerative diseases such as glioblastoma, and Alzheimer’s disease (AD). Conti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3309a687dfa538be8391e94425e4c921
https://doi.org/10.26434/chemrxiv-2023-rk8bf
https://doi.org/10.26434/chemrxiv-2023-rk8bf
Autor:
A. Sonia Petcu, Carlos Lázaro-Milla, F. Javier Rodríguez, Isabel Iriepa, Óscar M. Bautista-Aguilera, Cristina Aragoncillo, José M. Alonso, Pedro Almendros
Publikováno v:
The Journal of Organic Chemistry.
Autor:
Małgorzata Anna Marć, Annamária Kincses, Bálint Rácz, Muhammad Jawad Nasim, Muhammad Sarfraz, Carlos Lázaro-Milla, Enrique Domínguez-Álvarez, Claus Jacob, Gabriella Spengler, Pedro Almendros
Publikováno v:
Pharmaceuticals, Vol 13, Iss 12, p 453 (2020)
Multidrug resistance of cancer cells to cytotoxic drugs still remains a major obstacle to the success of chemotherapy in cancer treatment. The development of new drug candidates which may serve as P-glycoprotein (P-gp) efflux pump inhibitors is a pro
Externí odkaz:
https://doaj.org/article/25bd7f125872415da98e670dd65a55fc
Autor:
Cristina Aragoncillo, Irene Martín-Mejías, Carlos Lázaro-Milla, Shoki Hoshikawa, Takashi Matsumoto, Hikaru Yanai, Pedro Almendros
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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The carboarylation reaction of biphenyl-alkynes was successfully triggered by electrophilic attack of 1,1-bis(triflyl)ethylene on the alkyne moiety to give polycyclic aromatic hydrocarbons (PAHs) decorated by superacidic carbon acid functionality. Ne
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 818-826 (2013)
A combined experimental and computational study on regioselective gold-catalyzed synthetic routes to 1,3-oxazinan-2-ones (kinetically controlled products) and 1,3-oxazin-2-one derivatives (thermodynamically favored) from easily accessible allenic car
Externí odkaz:
https://doaj.org/article/d1de543605dd48cf922ad5d1b9236b62
Publikováno v:
Molecules, Vol 16, Iss 9, Pp 7815-7843 (2011)
The last decade has witnessed dramatic growth in the number of reactions catalyzed by gold complexes because of their powerful soft Lewis acid nature. In particular, the gold-catalyzed activation of propargylic compounds has progressively emerged in
Externí odkaz:
https://doaj.org/article/621a0a4d24f5415a811813ac8eada6c2
Autor:
Benito Alcaide, Pedro Almendros
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 7, Iss 1, Pp 622-630 (2011)
New gold-catalyzed methods using the β-lactam scaffold have been recently developed for the synthesis of different sized heterocycles. This overview focuses on heterocyclization reactions of allenic and alkynic β-lactams which rely on the activatio
Externí odkaz:
https://doaj.org/article/49ad30e491d647faa08d563adb2e68ec
Autor:
Pedro Almendros, Cristina Aragoncillo, Gema Cabrero, Ricardo Callejo, Rocío Carrascosa, Amparo Luna, Teresa Martínez del Campo, M. Carmen Pardo, M. Teresa Quirós, M. Carmen Redondo, Carolina Rodríguez-Ranera, Alberto Rodríguez-Vicente, M. Pilar Ruiz
Publikováno v:
ARKIVOC, Vol 2010, Iss 3, Pp 74-92 (2009)
Externí odkaz:
https://doaj.org/article/8405b104c0db47c3968dac2e7fc9eef9