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1.
Valls N Vallribera M López-Canet M Bonjoch J 《The Journal of organic chemistry》2002,67(14):4945-4950
The first total synthesis of aquatic peptide microcin SF608 is described. Coupling of L-Hpla with the dipeptide L-Phe-L-Choi followed by coupling with agmatine and a deprotection step gave microcin SF608. In addition, the levorotatory character of L-Hpla (5) was thoroughly established, and the conformational analysis of L-Choi containing peptides 1 and 8-10 was performed using NMR spectroscopy to examine the cis-trans isomer equilibrium of the L-Phe-L-Choi amide bond. 相似文献
2.
Molins Elies Roig Anna Miravitlles Carlos Moreno-Mañas Marcial Vallribera Adelina Gálvez Nicanor Serra Neus 《Structural chemistry》1998,9(3):203-208
The crystal and molecular structure of (BzlMe3N)
2
+
[Fe2OCl6]2- has been determined. The asymmetric unit contains two benzyltrimethylammonium cations and two half -oxo-bis(trichloro-iron(III)) anions. The bridging -oxygen atoms of these anions are located over crystallographic symmetry elements. Therefore, the two anions resulting from the symmetry operations correspond to two different conformers presenting angular and linear dispositions of the Fe-O-Fe bond angle. Mössbauer spectrum consists of two asymmetric lines that are adequately simulated by two equally populated quadrupole doublets associated with the two iron sites. 相似文献
3.
Ana Maria Montagut Albert Granados Anna Ballesteros Roser Pleixats Montserrat Llagostera Pilar Cortés Rosa María Sebastián Adelina Vallribera 《Tetrahedron》2019,75(1):102-108
Surface coating of metal nanoparticles is one of the major aspects to be optimized in the design of antimicrobial nanoparticles. The novelty of this work is that antimicrobial derivatives have been used as stabilizers to protect silver nanoparticles (Ag NPs). Microbicidal activity studies of fabricated cotton textiles coated with these Ag@Antibio were performed. Protective ligand layers of Ag NPs resulted to be a deterministic factor in their antimicrobial activity. The best bactericidal activity was obtained for Fabric TAM (coated with Ag NPs with triarylmethane derivates in surface, Ag@TAMSH), with a bacterial decrease of 3 log units for the S. aureus strain. Intrinsic antibiotic activity and partial positive charge of the TAMSH probably enhanced their antimicrobial effects. Fabric Eu (coated with Ag NPs with eugenol derivates in surface, Ag@EugenolSH) and Fabric FQPEG (coated with Ag NPs embedded in PEG-fluoroquinolone derivatives in surface, Ag@FQPEG) displayed antibacterial activity for both Staphylococcus aureus and Pseudomonas aeruginosa strains. These coated antimicrobial cotton fabrics can be applied in different medical textiles. 相似文献
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Some transition metal complexes of β-dicarbonyl compounds react with electrophiles at α-C. These reactions, carried out under
neutral conditions, offer a broader scope than their conventional counterparts, and are generally performed in the presence
of stoichiometric or catalytic amounts of strong bases. Mechanistic observations using different reaction conditions are also
relevant from a synthetic point of view.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 3, pp. 418–427, March, 1997. 相似文献
8.
Sandra Martínez Laura Martín Elies Molins Marcial Moreno-Ma?as Anna Roig Adelina Vallribera 《Monatshefte für Chemie / Chemical Monthly》2006,52(1):627-633
We prepared organic gels and organic and carbon aerogels doped with europium through sol–gel processes. Eu-gels were prepared
by sol–gel polymerization of the potassium salt of 2,4-dihydroxybenzoic acid with formaldehyde followed by ion-exchange with
Eu(OTf)3. Eu–organic aerogels were obtained after CO2 supercritical drying of the gels and Eu–carbon aerogels were obtained by pyrolysing the organic aerogels. The Eu-gels containing
12% europium proved to be efficient as recoverable catalyst in Michael additions. 相似文献
9.
Dr. Albert Granados Dr. Iván Rivilla Prof. Fernando P. Cossío Prof. Adelina Vallribera 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(35):8214-8218
A highly enantioselective catalytic method for the synthesis of quaternary α-trifluoromethyl derivatives of 3-oxo esters is described. The reaction uses lanthanum(III) triflate and chiral PyBOX-type C2-symmetric ligands to generate intermediate LaIII complexes that incorporate an enolate moiety of the starting 3-oxo ester and the trifluoromethylation transfer reagent. The enantioselectivity of the reaction stems from the efficient blockage of one of the prochiral faces of the LaIII enolate by one unit of the C2-symmetric ligand. 相似文献
10.
Valls N López-Canet M Vallribera M Bonjoch J 《Chemistry (Weinheim an der Bergstrasse, Germany)》2001,7(16):3446-3460
The first total syntheses of aeruginosin 298-A (1) and aeruginosin 298-B (3) are described. The syntheses of the alternative putative structures 2 and 4 were also accomplished. The key common strategic element is the stereo-controlled synthesis of (2S,3aS,6R,7aS)-6-hydroxyoctahydroindole-2-carboxylic acid (L-Choi, 5) from L-tyrosine. The synthesis of this new bicyclic alpha-amino acid, which is the core of aeruginosins, involves Birch reduction of O-methyl-L-tyrosine (6) and aminocyclization of the resulting dihydroanisole 7 in acid medium, followed by N-benzylation to give the diastereoisomers 12 and 13. Upon acid treatment with HCl-MeOH, the last two produce an equilibrium mixture in which the endo isomer 13 significantly predominates. Hydrogenation of 13 in the presence of (Boc)2O gives 16, which on reduction with LS-Selectride furnishes the alcohol 22, a protected L-Choi. Successive couplings of 22 with D-leucine, protected (R)-(4-hydroxyphenyl)lactic acid, and L-arginine fragments, followed by reduction to the argininol level and a deprotection end step complete the synthetic sequence to produce aeruginosin 298-A (1). Spectral comparison showed that peptide 2, with the structure previously proposed for aeruginosin 298-A, was different from the natural product. However, synthetic 1 was found to be identical to the isolated natural sample of aeruginosin 298-A. These results unequivocally establish that the absolute stereochemistry of aeruginosin 298-A, formerly assigned incorrectly, is D-Hpla-D-Leu-L-Choi-L-Argol, as shown by structure 1. Aeruginosin 298-B was also synthesized and shown to be a mixture of rotamers of D-Hpla-D-Leu-L-ChoiNH2 (3), rather than an epimeric mixture of 3 and the L-Leu-incorporating 4. 相似文献