Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Erik Lager"'
Autor:
Carlos A. Osorio-Martı́nez, Juan O. Flores-Rizo, Iñigo López Arbeloa, Brenda Daniela Gutierrez-Ramos, Rongrong Hu, Erik Lager, Ben Zhong Tang, Lourdes Betancourt-Mendiola, Arlette Urías-Benavides, Ismael J. Arroyo, Enrique Alvarado-Martínez, Ismael Valois-Escamilla, Teresa Arbeloa, José L. Belmonte-Vázquez, Jorge Bañuelos, Mayra R. Martinez-Gonzalez, Eduardo Peña-Cabrera, César F. A. Gómez-Durán
Publikováno v:
The Journal of Organic Chemistry. 80:5771-5782
Several new examples of meso-(het)arylBODIPY were prepared via the Liebeskind-Srogl (L-S) cross-coupling reaction of the Biellmann BODIPYs (1a,b) and aryl- and heteroarylboronic acids in good to excellent yield. It was shown that this reaction could
Publikováno v:
Tetrahedron Letters. 48:4215-4218
Z-Ligustilide, a naturally occurring phthalide isolated from Ligusticum porteri, underwent Diels-Alder reactions with different dienophiles yielding novel tricyclic products with potentially interesting biological properties. Where selectivity was po
Autor:
Elsebet Ø. Nielsen, Erik Lager, Pierre Andersson, Ingrid Pettersson, Jakob Nilsson, Olov Sterner, M. Nielsen, Tommy Liljefors
Publikováno v:
Journal of Medicinal Chemistry. 49:2526-2533
The 3-ethoxycarbonyl-4-quinolone compound 1 has previously been identified via a database search as an interesting lead compound for ligand binding at the benzodiazepine site of GABA(A) receptors (Kahnberg et al. J. Mol. Graphics Modelling 2004, 23,
Publikováno v:
The Journal of organic chemistry. 74(5)
A series of 14 meso-polyarylamine-BODIPY (borondipyrromethene) hybrids of the general structure A were synthesized. Two methods were used to prepare them. The first protocol involved a direct Liebeskind-Srogl cross-coupling of thiomethylbodipys 1-2 w
Autor:
Fabian Villanueva-Garcia, Rubi Zamudio‐Vazquez, Martha I. González-Domínguez, Eduardo Peña-Cabrera, Erik Lager, Angélica Aguilar-Aguilar, Jazmin Godoy‐Vargas
Publikováno v:
ChemInform. 39
An unprecedented synthesis of 8-substituted-borondipyrromethenes is described starting from 8-thiomethylbodipy 1. Aryl, heteroaryl, alkenyl, and organometallic boronic acids smoothly reacted with 1 in the presence of a catalytic amount of Pd(0) and a
Publikováno v:
Bioorganicmedicinal chemistry. 16(14)
The finding that alkyl 1,4-dihydro-4-oxoquinoline-3-carboxylate and N-alkyl-1,4-dihydro-4-oxoquinoline-3-carboxamide derivatives may be high-affinity ligands at the benzodiazepine binding site of the GABA(A) receptor, prompted a study of 3-acyl-1,4-d
Publikováno v:
ChemInform. 38
Autor:
Erik Lager, Angélica Aguilar-Aguilar, Martha I. González-Domínguez, Jazmin Godoy‐Vargas, Rubi Zamudio‐Vazquez, Fabian Villanueva-Garcia, Eduardo Peña-Cabrera
Publikováno v:
Organic letters. 9(20)
An unprecedented synthesis of 8-substituted-borondipyrromethenes is described starting from 8-thiomethylbodipy 1. Aryl, heteroaryl, alkenyl, and organometallic boronic acids smoothly reacted with 1 in the presence of a catalytic amount of Pd(0) and a
Autor:
Linda Camet, Celia Rosenberg, Erik Lager, Jette Schougaard, Pia Kahnberg, Tommy Liljefors, Olov Sterner, Elisabet Ostergaard Nielsen, Mogens Nielsen
Publikováno v:
Journal of medicinal chemistry. 45(19)
To further develop and evaluate a pharmacophore model previously proposed by Cook and co-workers (Drug Des. Discovery 1995, 12, 193-248) for ligands binding to the benzodiazepine site of the GABA(A) receptor, 40 new flavone derivatives have been synt
Foundation for a classification of collaboration levels for human-robot cooperation in manufacturing
Publikováno v:
Production and Manufacturing Research: An Open Access Journal, Vol 7, Iss 1, Pp 448-471 (2019)
Industry 4.0 aims to support the factory of the future, involving increased use of information systems and new ways of using automation, such as collaboration where a robot and a human share work on a single task. We propose a classification of colla
Externí odkaz:
https://doaj.org/article/795c0db2bf34448d9ade89b983e2a441