Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Carlos Díez-Poza"'
Publikováno v:
Marine Drugs, Vol 20, Iss 10, p 642 (2022)
Heterocycles are particularly common moieties within marine natural products. Specifically, tetrahydrofuranyl rings are present in a variety of compounds which present complex structures and interesting biological activities. Focusing on terpenoids,
Externí odkaz:
https://doaj.org/article/ba2c51556d264684aba74636a621a424
Publikováno v:
Marine Drugs, Vol 20, Iss 2, p 120 (2022)
Oxygen heterocycles are units that are abundant in a great number of marine natural products. Among them, marine polyketides containing tetrahydrofuran rings have attracted great attention within the scientific community due to their challenging stru
Externí odkaz:
https://doaj.org/article/0eead2ba4f1f4b87b6c73d84bba64886
Autor:
Carlos Díez-Poza, Asunción Barbero
Publikováno v:
Molecules, Vol 26, Iss 23, p 7386 (2021)
The regioselective ring opening of epoxy alcohols is an effective method for the synthesis of different types of oxacycles. The 5-exo opening being preferred vs. the 6-endo mode, according to Baldwin rules, the use of silyl-substituted oxiranes has b
Externí odkaz:
https://doaj.org/article/a6debb6a9f594556bc254acf10a4e436
Autor:
Paula González-Andrés, Laura Fernández-Peña, Carlos Díez-Poza, Carlos Villalobos, Lucía Nuñez, Asunción Barbero
Publikováno v:
Marine Drugs, Vol 19, Iss 2, p 78 (2021)
Intracellular Ca2+ plays a pivotal role in the control of a large series of cell functions in all types of cells, from neurotransmitter release and muscle contraction to gene expression, cell proliferation and cell death. Ca2+ is transported through
Externí odkaz:
https://doaj.org/article/803025b55d5140759cfdf1eda73ac0db
Publikováno v:
Marine Drugs, Vol 16, Iss 11, p 421 (2018)
Tetrahydropyrans are abundantly found in marine natural products. The interesting biological properties of these compounds and their analogues make necessary the development of convenient procedures for their synthesis. In this paper, an atom economy
Externí odkaz:
https://doaj.org/article/3318ce88b7f44b5b8e99798fa46ba821
Publikováno v:
Marine Drugs, Vol 15, Iss 11, p 361 (2017)
Oceans have shown to be a remarkable source of natural products. The biological properties of many of these compounds have helped to produce great advances in medicinal chemistry. Within them, marine natural products containing an oxepanyl ring are p
Externí odkaz:
https://doaj.org/article/95edb243163b4e259cbf80d07068f7d5
Autor:
Diego Jaraba Cabrera, Ryan D. Lewis, Carlos Díez-Poza, Lucía Álvarez-Miguel, Marta E. G. Mosquera, Alex Hamilton, Christopher J. Whiteoak
Publikováno v:
Dalton Transactions. 52:5882-5894
[InBr(salphen)] is identified as the most active catalyst for conversion of CO2 and epoxides to cyclic carbonates compared to the Al and Ga congeners. The elucidated mechanism highlights the importance of both Lewis acidity and ligand fluxionality.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71a17108bd297c7be0a358aa8681f54a
https://doi.org/10.1039/d3dt00089c
https://doi.org/10.1039/d3dt00089c
Heterocycles are particularly common moieties within marine natural products. Specifically, tetrahydrofuranyl rings are present in a variety of compounds which present complex structures and interesting biological activities. Focusing on terpenoids,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e94cd79fe5376b7a404f67ccf4389bc7
https://doi.org/10.20944/preprints202209.0320.v1
https://doi.org/10.20944/preprints202209.0320.v1
Publikováno v:
Arkivoc. 2020:96-116
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39e855770df36027ac42e1ee1da9a22e
https://doi.org/10.24820/ark.5550190.p011.111
https://doi.org/10.24820/ark.5550190.p011.111
Publikováno v:
Comprehensive Heterocyclic Chemistry IV ISBN: 9780128186565
Comprehensive Heterocyclic Chemistry IV
Comprehensive Heterocyclic Chemistry IV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb736468c28b48b0537a599e1d038e5e
https://doi.org/10.1016/b978-0-12-409547-2.14894-2
https://doi.org/10.1016/b978-0-12-409547-2.14894-2