The Research for Introducing Gem-Difluoromethylene Group into the Organic Molecules

2014 ◽  
Vol 881-883 ◽  
pp. 196-200 ◽  
Author(s):  
Chao Fang ◽  
Fan Hong Wu

The article mainly argues with the latest progress of methodologies which is the introduction of a difluoromethylene unit into the organic compounds. It will also summarize the theoretical study of introducing gem-difluoromethylene group into the organic molecular. Firstly, it briefly reviews the function of difluoromethylation reaction; secondly, we start to study the recent development of introducing a CF2group in the organic synthesis. At last but not the least, we conclude the use of the new CF2unit in the syntheis of the molecular.

2018 ◽  
Vol 34 (1) ◽  
pp. 57
Author(s):  
Diana Rocha ◽  
Jacqueline Aparecida Takahashi ◽  
Maria Amelia Diamantino Boaventura

The use of microorganisms to induce chemical modifications in organic molecules is a very useful tool in organic synthesis, to obtain biologically active substances. The fungus Cephalosporium aphidicola is known by its ability to hydroxylate several skeleton positions of many classes of organic compounds. In this work, the microbial transformation of ent-kaur-16-en-19-ol (1) by C. aphidicola, afforded two hydroxylated compounds, ent-kauran-16b,19-diol (2) and ent-kauran-16b,17,19-triol (3). Their structures were established by 1D and 2D-NMR studies. Both compounds were tested for their action on the growth of radical and shoot of Lactuca sativa.


2000 ◽  
Vol 65 (1) ◽  
pp. 47-57 ◽  
Author(s):  
Pavel Hradil ◽  
Jiří Votinský ◽  
Karel Komárek ◽  
Vítězslav Zima ◽  
Jaroslava Kalousová ◽  
...  

Gas chromatographic measurement of specific retention volumes of vapours of selected groups of organic compounds has been used to determine differential molar enthalpy of adsorption of their molecules on the surface of layered vanadyl phosphate substituted with ferric ions having the composition of [Fe(H2O)]0.20(VO)0.80PO4. Various types of bonds of the molecules to the surface of the layered adsorbent including their probable orientation with respect to the layers have been discussed. It was observed a dependence of the specific peak elution volume and shape of chromatographic peak on the sample size in the cases of those compounds whose molecules are chemically bound to the adsorbent surface. A connection is pointed out between the adsorption strength of the organic molecules on the layered adsorbent and the tendency of the system to undergo intercalation reaction.


Author(s):  
Guobing Yan ◽  
Kaiying Qiu ◽  
Ming Guo

The C-F bond is the strongest single bond in organic compounds. It is the most challenging task to study the activation of C-F bond in organic synthesis. Trifluoromethyl-containing compounds, which...


2012 ◽  
Vol 162 (7-8) ◽  
pp. 641-649 ◽  
Author(s):  
Ming-Kuan Yan ◽  
Chao Zheng ◽  
Jun Yin ◽  
Zhong-Fu An ◽  
Run-Feng Chen ◽  
...  

2021 ◽  
Vol 18 ◽  
Author(s):  
Aparna Das

: In recent years, photocatalytic technology has shown great potential as a low-cost, environmentally friendly, and sustainable technology. Compared to other light sources in photochemical reaction, LEDs have advantages in terms of efficiency, power, compatibility, and environmentally-friendly nature. This review highlights the most recent advances in LED-induced photochemical reactions. The effect of white and blue LEDs in reactions such as oxidation, reduction, cycloaddition, isomerization, and sensitization is discussed in detail. No other reviews have been published on the importance of white and blue LED sources in the photocatalysis of organic compounds. Considering all the facts, this review is highly significant and timely.


2001 ◽  
Vol 19 (3) ◽  
pp. 237-244 ◽  
Author(s):  
Nikolai V. Nikolenko

The energies of unoccupied and occupied orbitals were used as the correlation parameters between the electronic and adsorptive properties of organic molecules. A model describing the chemisorption of organic compounds on CaCO3 involving two types of interaction, i.e. two-electron, donor–acceptor interaction HOMO(adsorbent) → LUMO(adsorbate) and four-electron, three-orbital interaction HOMO(adsorbent) → {LUMO(adsorbate) + HOMO(adsorbate)}, was proposed. It was concluded that strengthening of the bond involved in chemisorption occurred if the energies of the occupied orbitals associated with the adsorbate and adsorbent were concurrent.


2021 ◽  
Author(s):  
Stephan P Blum ◽  
Kamil Hofman ◽  
Georg Manolikakes ◽  
Siegfried R Waldvogel

Organic photo- and electrochemistry currently experience tremendous attention in organic synthesis as both techniques enable reagent-less activation of organic molecules without using expensive and hazardeous redox reagents. The incorporation of...


2019 ◽  
Author(s):  
Nikita A. Ivanov ◽  
Yimo Liu ◽  
Sven Kochmann ◽  
Sergey N. Krylov

<div>Continuous-flow organic synthesis naturally requires continuous-flow separation of reaction components. The most common continuous-flow separation approach is liquid-liquid extraction based on differential distribution of molecules between organic and aqueous phases. This approach has limited selectivity; it can hardly separate different hydrophobic organic molecules from each other. Continuous-flow electrophoresis can facilitate much more selective separation in a single phase, but it is currently limited to aqueous electrolytes which are incompatible with many hydrophobic organic molecules. Further, water electrolysis in aqueous electrolytes results in generation of large volumes of gas making steady-state operation a major technical challenge. Here, we introduce non-aqueous continuous-flow electrophoresis (NACFE) in which the electrolyte is a solution of an organic salt in an aprotic organic solvent. We demonstrate that NACFE can maintain stable separation of multiple species during 10 hours. The non-aqueous nature of NACFE and its ability to support steady-state operation make it suitable for its incorporation into continuous-flow organic synthesis.</div>


2021 ◽  
Author(s):  
Teresa Fornaro ◽  
Giovanni Poggiali ◽  
Maria Angela Corazzi ◽  
Cristina Garcia ◽  
Giulia Dimitri ◽  
...  

&lt;div&gt;&amp;#160;&lt;/div&gt; &lt;p&gt;&lt;strong&gt;Abstract&lt;/strong&gt;&lt;/p&gt; &lt;p&gt;We present laboratory activities of preparation, characterization, and UV irradiation processing of Mars soil analogues, which are key to support both in situ exploration and sample return missions devoted to detection of molecular biosignatures on Mars.&lt;/p&gt; &lt;p&gt;In detail we prepared analog mineral samples relevant to the landing sites of past, present and future Mars exploration missions, such as Gale Crater, Jezero Crater, and Oxia Planum. We doped these samples with a large variety of organic molecules (both biotic and prebiotic molecules) like amino acids, nucleotides, monosaccharides, aldehydes, lipids. We investigated molecular photostability under UV irradiation by monitoring in situ possible modifications of infrared spectroscopic features. These investigations provide pivotal information for ground analysis carried out by rovers on Mars.&lt;/p&gt; &lt;p&gt;&lt;strong&gt;Introduction&lt;/strong&gt;&lt;/p&gt; &lt;p&gt;Laboratory simulations of Mars are key to support the scientific activity and technology development of life detection instruments on board present and upcoming rover missions such as Mars2020 Perseverance [1] and ExoMars2022 Rosalind Franklin [2]. Studies about the stability of organic molecules in a Martian-like environment allow us to explore the conditions for the preservation of molecular biosignatures and develop models for their degradation in the Martian geological record. A systematic study of the effects of UV radiation on a variety of molecule-mineral complexes mimicking Martian soil can be key for the selection of the most interesting samples to analyse in situ or/and collect for sample return. Testing the sensitivity of different techniques for detection of the diagnostic features of molecular biosignatures embedded into mineral matrices as a function of the molecular concentration helps the choice, design and operation of flight instruments, as well as the interpretation of data collected on the ground during mission operative periods.&lt;/p&gt; &lt;p&gt;&lt;strong&gt;Methods&lt;/strong&gt;&lt;/p&gt; &lt;p&gt;Experimental analyses were conducted in the Astrobiology Laboratory at INAF-Astrophysical Observatory of Arcetri (Firenze, Italy). Laboratory activities pertain to: (i) synthesis of Mars soil analogues doped with organic compounds that are considered potential molecular biosignatures; (ii) UV-irradiation processing of the Mars soil analogues under Martian-like conditions; and (iii) spectroscopic characterization of the Mars soil analogues.&lt;/p&gt; &lt;p&gt;&lt;strong&gt;Results&lt;/strong&gt;&lt;/p&gt; &lt;p&gt;Such studies have shown to be very informative in identifying mineral deposits most suitable for preservation of organic compounds, while highlighting the complementarity of different techniques for biomarkers detection, which is critical for ensuring the success of space missions devoted to the search for signs of life on Mars.&lt;/p&gt; &lt;p&gt;We will present a series of laboratory results on molecular degradation caused by UV on Mars and possible application to detection of organics by Martian rovers [3,4,5,6]. In detail, we investigated the photostability of several amino acids like glycine, alanine, methionine, valine, tryptophan, phenylalanine, glutamic acid, prebiotic molecules like urea, deoxyribose and glycolaldehyde, and biomarkers like nucleotides and phytane adsorbed on relevant Martian analogs. We monitored the degradation of these molecule-mineral complexes through in situ spectroscopic analysis, investigating the reflectance properties of the samples in the NIR/MIR spectral region. Such spectroscopic characterization of molecular alteration products provides support for two upcoming robotic missions to Mars that will employ NIR spectroscopy to look for molecular biosignatures, through the instruments SuperCam on board Mars 2020, ISEM, Ma_MISS and MicrOmega on board ExoMars 2022.&lt;/p&gt; &lt;p&gt;&lt;strong&gt;Acknowledgements&lt;/strong&gt;&lt;/p&gt; &lt;p&gt;This research was supported by the Italian Space Agency (ASI) grant agreement ExoMars n. 2017-48-H.0.&lt;/p&gt; &lt;p&gt;&lt;strong&gt;References&lt;/strong&gt;&lt;/p&gt; &lt;p&gt;[1] Farley K. A. et al. (2020) Space Sci. Rev. 216, 142.&lt;/p&gt; &lt;p&gt;[2] Vago, J. L. et al. (2017) Astrobiology 6, 309&amp;#8211;347.&lt;/p&gt; &lt;p&gt;[3] Fornaro T. et al. (2013) Icarus 226, 1068&amp;#8211;1085.&lt;/p&gt; &lt;p&gt;[4] Fornaro T. et al. (2018) Icarus 313, 38-60.&lt;/p&gt; &lt;p&gt;[5] Fornaro T. et al. (2020) Front. Astron. Space Sci. 7:539289.&lt;/p&gt; &lt;p&gt;[6] Poggiali G. et al. (2020) Front. Astron. Space Sci. 7:18.&lt;/p&gt;


2021 ◽  
Vol 25 ◽  
Author(s):  
Saima malik ◽  
Aditya G. Lavekar ◽  
Bimal Krishna Banik

: The radical was first come into existence in 1900 by Gomberg, where the triphenylmethane radical was explored. Thus, even to date, two centuries have seen radical chemistry as the methodology of preference in organic synthesis. Due to the fascinating nature of the radical-mediated cyclization reactions, it always caught the eye of organic chemists for the synthesis of novel organic compounds with diverse stereochemistry. Moreover, the development of radical methods further proves beneficial for the synthesis by providing atom- and step-economical methods to complex molecules. Among these, where radical chemistry has been employed, the use of tin-based radical annulation is the most common and widely used field for the synthesis of a wide range of organic reactions with medicinal importance. In this review, we compiled recent tin-mediated radical cyclization reactions toward the synthesis of molecules of biological significance.


Sign in / Sign up

Export Citation Format

Share Document