Zobrazeno 1 - 10
of 623
pro vyhledávání: '"Carlos Cativiela"'
Autor:
Esteban P. Urriolabeitia, Pablo Sánchez, Alexandra Pop, Cristian Silvestru, Eduardo Laga, Ana I. Jiménez, Carlos Cativiela
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 1111-1123 (2020)
The stereoselective synthesis of truxillic bis-amino esters from polyfunctional oxazolones is reported. The reaction of 4-((Z)-arylidene)-2-(E)-styryl-5(4H)-oxazolones 2 with Pd(OAc)2 resulted in ortho-palladation and the formation of a dinuclear ope
Externí odkaz:
https://doaj.org/article/fee42e17edf94f3799c87cf965ce4dcd
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 2597-2601 (2018)
A straightforward synthetic entry to functionalized hydrindane compounds based on a rapid assembly of the core nucleus by a Danheiser cycloaddition is reported. Valuable bicyclic building blocks containing the fused five and six-membered carbocyclic
Externí odkaz:
https://doaj.org/article/eb6069ca9b934460bf0225cd5d54b39b
Autor:
Nawal Mahfoudh, Nagore I. Marín-Ramos, Ana M. Gil, Ana I. Jiménez, Duane Choquesillo-Lazarte, Daniel F. Kawano, Joaquín M. Campos, Carlos Cativiela
Publikováno v:
Arabian Journal of Chemistry, Vol 11, Iss 3, Pp 426-441 (2018)
Two distinct series of the 3-amino-1,5-benzoxathiepin scaffold, derived from L-cysteine, were synthesized and evaluated for their anti-proliferative activity in the breast cancer MDA-MB-231 and MCF-7 cells, and in the ovarian carcinoma SKOV-3 cell li
Externí odkaz:
https://doaj.org/article/ee6ab566430a4b0f80dc18e9ef7a4fe6
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
The novel enantiopure synthesis of protected proline-cysteine analogs by means of 1,3-dipolar cycloaddition of homochiral thiazolines and azomethine ylides is described. The important role of the oxidation state of the sulfur atom of the dipolarophil
Autor:
Dennis Kühbeck, Basab Bijayi Dhar, Eva-Maria Schön, Carlos Cativiela, Vicente Gotor-Fernández, David Díaz Díaz
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 1111-1118 (2013)
The activity of gelatin and collagen proteins towards C–C bond formation via Henry (nitroaldol) reaction between aldehydes and nitroalkanes is demonstrated for the first time. Among other variables, protein source, physical state and chemical modif
Externí odkaz:
https://doaj.org/article/c781aff0170846fb9c0635cf38bc894f
Autor:
Ana I. Jiménez, Esteban P. Urriolabeitia, Cristian Silvestru, Alexandra Pop, Eduardo Laga, Pablo Sánchez, Carlos Cativiela
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 1111-1123 (2020)
Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname
Beilstein Journal of Organic Chemistry
Digital.CSIC. Repositorio Institucional del CSIC
Zaguán: Repositorio Digital de la Universidad de Zaragoza
Universidad de Zaragoza
Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname
Beilstein Journal of Organic Chemistry
Digital.CSIC. Repositorio Institucional del CSIC
Zaguán: Repositorio Digital de la Universidad de Zaragoza
Universidad de Zaragoza
The stereoselective synthesis of truxillic bis-amino esters from polyfunctional oxazolones is reported. The reaction of 4-((Z)-arylidene)-2-(E)-styryl-5(4H)-oxazolones 2 with Pd(OAc)2 resulted in ortho-palladation and the formation of a dinuclear ope
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
Here we report the diastereopure synthesis of a novel protected lanthionine derivative substituted with a cyclohexane ring as well as the diastereopure synthesis of an α-methyllanthionine derivative. By starting from enantiopure α,β-cyclohexane-su
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 8, Iss 1, Pp 1569-1575 (2012)
A new method for the regioselective synthesis of 2-alkoxycarbonyl- and 2-(aminocarbonyl)phenylglycinate methyl esters has been developed. The reaction of the orthopalladated complex [Pd(μ-Cl)(C6H4(CH(CO2Me)NMe2)-2)]2 (1) with nucleophiles HNu under
Externí odkaz:
https://doaj.org/article/d2ff8c2c60894658bd40e84405145f01
Publikováno v:
ARKIVOC, Vol 2007, Iss 4, Pp 157-169 (2006)
Externí odkaz:
https://doaj.org/article/a9b150eaf5384264bc736775daffe8a0
Publikováno v:
ARKIVOC, Vol 2005, Iss 6, Pp 46-61 (2005)
Externí odkaz:
https://doaj.org/article/97dabafae59043f49779615077bfddc6