H2O2 direct synthesis under mild conditions on Pd–Au samples: Effect of the morphology and of the composition of the metallic phase

2015 ◽  
Vol 248 ◽  
pp. 18-27 ◽  
Author(s):  
Federica Menegazzo ◽  
Maela Manzoli ◽  
Michela Signoretto ◽  
Francesco Pinna ◽  
Giorgio Strukul
Keyword(s):  
Direct Synthesis ◽  
Metallic Phase ◽  
Mild Conditions ◽  
H2o2 Direct Synthesis

scholarly journals Recent Advances in Rapid Synthesis of Non-proteinogenic Amino Acids from Proteinogenic Amino Acids Derivatives via Direct Photo-Mediated C–H Functionalization

Molecules ◽  
2020 ◽  
Vol 25 (22) ◽  
pp. 5270
Author(s):  
Zhenbo Yuan ◽  
Xuanzhong Liu ◽  
Changmei Liu ◽  
Yan Zhang ◽  
Yijian Rao
Keyword(s):  
Amino Acids ◽  
Direct Synthesis ◽  
Environmentally Friendly ◽  
Powerful Method ◽  
Rapid Synthesis ◽  
Conservation Of Energy ◽  
Mild Conditions ◽  
Recent Advances ◽  
Recent Developments

Non-proteinogenic amino acids have attracted tremendous interest for their essential applications in the realm of biology and chemistry. Recently, rising C–H functionalization has been considered an alternative powerful method for the direct synthesis of non-proteinogenic amino acids. Meanwhile, photochemistry has become popular for its predominant advantages of mild conditions and conservation of energy. Therefore, C–H functionalization and photochemistry have been merged to synthesize diverse non-proteinogenic amino acids in a mild and environmentally friendly way. In this review, the recent developments in the photo-mediated C–H functionalization of proteinogenic amino acids derivatives for the rapid synthesis of versatile non-proteinogenic amino acids are presented. Moreover, postulated mechanisms are also described wherever needed.

scholarly journals High-Active Metallic-Activated Carbon Catalysts for Selective Hydrogenation

2018 ◽  
Vol 2018 ◽  
pp. 1-11 ◽  
Author(s):  
Nicolás Carrara ◽  
Carolina Betti ◽  
Fernando Coloma-Pascual ◽  
María Cristina Almansa ◽  
Laura Gutierrez ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Selective Hydrogenation ◽  
Nickel Catalysts ◽  
Metallic Phase ◽  
Hydrogen Chemisorption ◽  
Electronic Effects ◽  
X Ray ◽  
Mild Conditions ◽  
Temperature Programmed ◽  
Carbon Catalysts

A series of low-loaded metallic-activated carbon catalysts were evaluated during the selective hydrogenation of a medium-chain alkyne under mild conditions. The catalysts and support were characterized by ICP, hydrogen chemisorption, Raman spectroscopy, temperature-programmed desorption (TPD), temperature-programmed reduction (TPR), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR micro-ATR), transmission electronic microscopy (TEM), and X-ray photoelectronic spectroscopy (XPS). When studying the effect of the metallic phase, the catalysts were active and selective to the alkene synthesis. NiCl/C was the most active and selective catalytic system. Besides, when the precursor salt was evaluated, PdN/C was more active and selective than PdCl/C. Meanwhile, alkyne is present in the reaction media, and geometrical and electronic effects favor alkene desorption and so avoid their overhydrogenation to the alkane. Under mild conditions, nickel catalysts are considerably more active and selective than the Lindlar catalyst.

Some aspects of the formation and structural features of low nuclearity heterometallic carboxylates

2020 ◽  
Vol 92 (7) ◽  
pp. 1093-1110 ◽  
Author(s):  
Aleksey A. Sidorov ◽  
Natalia V. Gogoleva ◽  
Evgeniya S. Bazhina ◽  
Stanislav A. Nikolaevskii ◽  
Maksim A. Shmelev ◽  
...  
Keyword(s):  
Ligand Exchange ◽  
Direct Synthesis ◽  
Molecular Complexes ◽  
Structural Features ◽  
Exchange Reactions ◽  
Metal Core ◽  
Mild Conditions ◽  
Metal Organic ◽  
Heterometallic Carboxylates ◽  
Molecular Compounds

AbstractHeterometallic carboxylate complexes are of paramount interest in pure and applied coordination chemistry. Despite that plurality of such type compounds have been published to date, synthetic aspects of their chemistry often remain in the shadow of intriguing physical properties manifesting by these species. Present review summarizes reliable data on direct synthesis of low nuclearity molecular compounds as well as coordination polymers on their base with carboxylate-bridged {M2Mg} (M = Co2+, Ni2+, Cd2+), {M2Li2} (M = Co2+, Ni2+, Zn2+, VO2+), {M2Ln2} and {M2Ln} (M = Cu2+, Zn2+, Co2+) metal cores. Structural features and stabilization factors are considered and principal outcomes are confirmed by quantum-chemical calculations. Particular attention is paid to consideration of ligand-exchange reactions that allow controllable modification of heterometallic metal core under mild conditions giving diverse molecular complexes with modified ligand environment or Metal-Organic Frameworks with permanent porosity.

scholarly journals Rapid and Mild Synthesis of Au-NHC Complexes in a Simple Two-Phase Flow Reactor

2021 ◽  
Author(s):  
Helgi Freyr Jónsson ◽  
Anne Fiksdahl ◽  
Andrew Harvie
Keyword(s):  
Two Phase Flow ◽  
Flow Reactor ◽  
Direct Synthesis ◽  
Phase Flow ◽  
Rapid Synthesis ◽  
Two Phase ◽  
Second Stage ◽  
Mild Conditions ◽  
Common Problems

<p>We describe a simple two-phase flow reactor which allows for the efficient and rapid synthesis of several Au(I)-NHC complexes under mild conditions, with minimal workup, and avoiding common problems with decomposition to Au(0). An optional second stage allows for direct synthesis of Au(III)-NHC complexes, without isolation of the Au(I)-NHC intermediate.</p>

scholarly journals PIDA-mediated intramolecular oxidative C–N bond formation for the direct synthesis of quinoxalines from enaminones

RSC Advances ◽  
2019 ◽  
Vol 9 (14) ◽  
pp. 7718-7722 ◽  
Author(s):  
Hong Zhang ◽  
Jinhai Shen ◽  
Zhenhui Yang ◽  
Xiuling Cui
Keyword(s):  
Direct Synthesis ◽  
Bond Formation ◽  
Hypervalent Iodine ◽  
Mild Conditions

An expedient hypervalent iodine(iii)-mediated approach to obtain substituted quinoxalines from readily available enaminones has been developed under mild conditions.

Direct Synthesis of 5-Acyl-3-oxy-4-pyrones Based On Acid-­Catalyzed Acylation of Enaminodiones with Acylbenzotriazoles via Soft Enolization

Synthesis ◽  
2020 ◽  
Vol 52 (15) ◽  
pp. 2267-2276 ◽  
Author(s):  
Dmitrii L. Obydennov ◽  
Viktoria V. Viktorova ◽  
Elena V. Chernyshova ◽  
Alexander S. Shirinkin ◽  
Sergey A. Usachev ◽  
...  
Keyword(s):  
Ring Opening ◽  
Direct Synthesis ◽  
Pyrone Ring ◽  
Mild Conditions ◽  
Soft Enolization ◽  
Acid Catalyzed

A novel convenient acid-catalyzed acylation of enaminodiones with acylbenzotriazoles via soft enolization has been developed for the direct synthesis of hard-to-reach 5-acyl-3-oxy-4-pyrones. The important advantages of the reaction include broad substrate scope, mild conditions, scalability, and readily isolation of products by crystallization without the use of chromatography. Further modification of the pyrone ring and synthesis of various azaheterocycles via ring-opening transformation have been demonstrated for the preparation of potential scaffolds for inhibition of metalloenzymes.

Direct Synthesis of N-Functionalized Dipropargylamine Linkers as Models for Use in Peptide Stapling

Synlett ◽  
2019 ◽  
Vol 30 (19) ◽  
pp. 2153-2156
Author(s):  
Andrea Renzetti ◽  
Ryan N. Rutherford ◽  
Kozo Fukumoto ◽  
Dominique Kunciw ◽  
Hannah F. Sore ◽  
...  
Keyword(s):  
Direct Synthesis ◽  
Quantitative Yield ◽  
Mild Conditions ◽  
One Step ◽  
Peptide Stapling

N-Substituted dipropargylamines that are suitable as functionalized linkers for peptide stapling can be synthesized in one step under mild conditions from commercially available starting materials (41% to quantitative yield).

Direct Synthesis of Propylene from Ethylene over Palladium Containing Catalysts: Influence of the Support Nature

2015 ◽  
Vol 1085 ◽  
pp. 17-22 ◽  
Author(s):  
Luiza F. Sayfulina ◽  
Eygeny A. Buluchevskiy ◽  
Alexander V. Lavrenov ◽  
Tatyana I. Gulyaeva ◽  
Michael D. Trenikhin ◽  
...  
Keyword(s):  
Atmospheric Pressure ◽  
Direct Synthesis ◽  
Ethylene Dimerization ◽  
Mild Conditions ◽  
Propylene Yield

An influence of support acidity on the dimerization function on Pd-containing catalysts was studied. After addition of Re2O7 to PdO/SZ as ethylene dimerization catalyst with high butene-2 selectivity the obtained PdO-Re2O7/SZ catalyst was tested in direct synthesis of propylene from ethylene under mild conditions (40°C and atmospheric pressure). Propylene yield was approximately 45%, which is close to equilibrium one.

Additive- and Oxidant-Free Expedient Synthesis of Benzimidazoles Catalyzed by Cobalt Nanocomposites on N-Doped Carbon

Synlett ◽  
2019 ◽  
Vol 30 (03) ◽  
pp. 319-324 ◽  
Author(s):  
Zhaozhan Wang ◽  
Tao Song ◽  
Yong Yang
Keyword(s):  
Functional Group ◽  
Direct Synthesis ◽  
Biologically Active ◽  
One Pot ◽  
Mild Conditions ◽  
Wide Range ◽  
High Yields

A one-pot direct synthesis of a wide range of biologically active benzimidazoles through coupling of phenylenediamines and aldehydes catalyzed by a highly recyclable nonnoble cobalt nanocomposite was developed. A broad set of benzimidazoles can be efficiently synthesized in high yields and with good functional-group tolerance under additive- and oxidant-free mild conditions. The catalyst can be easily recycled for successive uses, and the process permits gram-scale syntheses of benzimidazoles.

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