Zobrazeno 1 - 8
of 8
pro vyhledávání: '"José C. Barcia"'
Autor:
Ricardo A. Tapia, Jacobo Cruces, Mauricio Cuellar, Juan C. Estévez, Cristian O. Salas, Ramón J. Estévez, José C. Barcia
Publikováno v:
Minerva. Repositorio Institucional de la Universidad de Santiago de Compostela
instname
SynOpen, Vol 01, Iss 01, Pp 0156-0165 (2017)
instname
SynOpen, Vol 01, Iss 01, Pp 0156-0165 (2017)
Here we describe modified syntheses of o-acetylbenzoic acids and o-acetylphenylacetic acids by Heck palladium-catalysed arylation of n-butyl vinyl ether with o-iodobenzoic acids or with o-iodophenylacetic acids, respectively. General syntheses of ben
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22e3e7cfe4e026637c6abd83fe3165d5
http://hdl.handle.net/10347/22517
http://hdl.handle.net/10347/22517
Autor:
José C. Barcia, José M. Otero, Juan C. Estévez, Cristian O. Salas, Ramón J. Estévez, Pablo Thomas
Publikováno v:
Tetrahedron. 68:1612-1621
A strategy for the synthesis of the novel (6b R ,7 R ,8 S ,9 S ,10 S ,10a R )-8-(benzyloxy)-7,9,10-trihydroxy-6b,7,8,9,10,10a-hexahydro-11 H -benzo[ a ]carbazole-5,6-dione is reported. The key steps were the Michael addition of 2-hydroxy-1,4-naphthoq
Publikováno v:
Synlett. 2007:1399-1402
We describe herein preliminary results on the novel Michael addition of naphthoquinones to nitroolefins and its application to the first synthesis of the novel (6b R,10a S)-7,8,9,10,10a,11-hexahydro-6b H-benzo[ A]carbazole-5,6-diones and (4a R,11b S)
Publikováno v:
Tetrahedron: Asymmetry. 16:11-14
The first total synthesis of (1 R ,2 S ,3 S ,4 R ,4a S ,11b S )-2-(benzyloxy)-1,2,3,4,4a,5-hexahydro-1,3,4-trihydroxy-11b H -benzo[ b ]carbazole-6,11-dione from D -glucose is described. The key steps of this synthesis are the stereoselective Michael
Publikováno v:
Tetrahedron Letters. 43:5141-5144
We describe here a new, efficient general synthesis of o -acetylbenzoic acids by Heck palladium-catalyzed arylation of n -butyl vinyl ether with o -bromobenzoic acid esters and the use of these compounds as starting materials for the synthesis of 3-b
Autor:
Amalia M. Estévez, José C. Barcia, Ana Martínez, Fernando Ataulfo González Fernández, Lucia Gonzalez, Ramón J. Estévez, Juan C. Estevez
Publikováno v:
Tetrahedron Letters. 48:2147-2149
A novel intramolecular palladium-mediated arylation approach to benzo[b]fluoren-11-ones has been investigated. This approach involves the novel oxidation of the key starting 2-(2′-bromobenzyl)naphthols to 2-(2′-bromobenzyl)-1,4-naphthoquinones, f
Publikováno v:
ChemInform. 33
We describe here a new, efficient general synthesis of o -acetylbenzoic acids by Heck palladium-catalyzed arylation of n -butyl vinyl ether with o -bromobenzoic acid esters and the use of these compounds as starting materials for the synthesis of 3-b
Autor:
Jose C. Barcia, Jacobo Cruces, Cristian O. Salas, Juan C. Estévez, Mauricio A. Cuellar, Ricardo A. Tapia, Ramón J. Estévez
Publikováno v:
SynOpen, Vol 01, Iss 01, Pp 0156-0165 (2017)
Abstract Here we describe modified syntheses of o-acetylbenzoic acids and o-acetylphenylacetic acids by Heck palladium-catalysed arylation of n-butyl vinyl ether with o-iodobenzoic acids or with o-iodophenylacetic acids, respectively. General s
Externí odkaz:
https://doaj.org/article/70861953fe5f454ba750c90cba9d27e7