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Methanol Synthesis
Methanol Synthesis

Alcohols
Alcohols

... The longest chain contains six carbon atoms, but it does not contain the carbon bonded to the hydroxyl group. The longest chain containing the carbon bonded to the —OH group is the one outlined by the green box, containing five carbon atoms. This chain is numbered from right to left in order to give ...
Unit 13: Organic Chemistry
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... Amines • Amines contain nitrogen atoms bonded to carbon atoms • They are named with the suffix –amine • Amines are slightly less polar than alcohols • They often have strong, offensive odors (like dead fish) ...
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Research on Hydrogenation of FAME to Fatty Alcohols
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... velocity increased. Compared with 0.15~0.4h-1 space velocity which calculated according to tradition process of hydrogenolysis of fatty acid methyl ester, supercritical reaction technology was taken, but there was 90% solvent remaining in reaction materials. When the space velocity of mixture made o ...
Montmorillonite: An efficient, heterogeneous and
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... interests to expandable montmorillonite clays [8, 9] and almost all of their clay catalysts have been either (a) acidtreated clays such as K-10 [10] or ion-exchanged clays such as Al3+, Cr3+ or H+ exchanged Wyoming or Texas bentonites [11]. The acid-treated and cation exchanged clays can be simply r ...
Computational Docking Experiments to Find a Ligand that Will Bind
Computational Docking Experiments to Find a Ligand that Will Bind

... sequentially replaced each peripheral carbonyl group by a sulfur atom (a less polar atom), followed by an aldehyde and a carboxylic acid groups (more polar groups) to obtain different derivatives of uric acid. The values of affinity energies for the three derivatives with all three peripheral carbon ...
IOSR Journal of Applied Chemistry (IOSR-JAC) e-ISSN: 2278-5736.
IOSR Journal of Applied Chemistry (IOSR-JAC) e-ISSN: 2278-5736.

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2009 Final Exam - Department of Chemistry | Oregon State University
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無投影片標題

0922089
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... in the presence of wide variety of functional groups. Several organometallic reagents are used for analogous cross-coupling reactions but organoboron compounds are interesting reagents because they are thermally stable, inert to water and oxygen and thus easy to handle. In addition, inorganic by-pro ...
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Lecture 10 Carbon-Nitrogen Bonds Formation I
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... Compounds that are enolic or potentially enolic react with a mixture of aldehydes and primary or secondary amine in the presence of an acid to afford amine salt which, after basification, gives an aminomethyl derivative. The reaction has found wide applications in organic synthesis. For example, the ...
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... HClO4(aq) + H2O(l) ---> H3O+(aq) + ClO4-(aq) HNO3(aq) + H2O(l) ---> H3O+(aq) + NO3-(aq) HCl(aq) + H2O(l) ---> H3O+(aq) + Cl-(aq) HBr(aq) + H2O(l) ---> H3O+(aq) + Br-(aq) HI(aq) + H2O(l) ---> H3O+(aq) + I-(aq) H2SO4(aq) + 2 H2O(l) ---> 2 H3O+(aq) + SO42-(aq) ...
Today`s literature presentation = 2/5th trivia + 2/5th
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CHEMISTRY 1000
CHEMISTRY 1000

... We’ve already seen one reaction which organic chemists would consider to be a reduction reaction – the nucleophilic addition of hydrogen to a carbonyl (using NaBH4 or LiAlH4 as the source of nucleophilic hydrogen). This was a chemoselective reaction – in other words, the reducing agent only reduced ...
cycloadditions with singlet oxygen
cycloadditions with singlet oxygen

... was not the main cause of selectivity since the tert-butyl group at R3 did not increase syn / anti selectivity (entry 2).21 Entries 3 and 4 seemed to support a stepwise mechanism. With R1=OMe, the electron-rich olefin was farther from the directing hydroxyl group and a decreased selectivity was obs ...
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Petasis reaction



The Petasis reaction (alternatively called the Petasis borono–Mannich (PBM) reaction) is the chemical reaction of an amine, aldehyde, and vinyl- or aryl-boronic acid to form substituted amines.Reported in 1993 by Nicos Petasis as a practical method towards the synthesis of a geometrically pure antifungal agent, naftifine, the Petasis reaction can be described as a variation of the Mannich reaction. Rather than generating an enolate to form the substituted amine product, in the Petasis reaction, the vinyl group of the organoboronic acid serves as the nucleophile. In comparison to other methods of generating allyl amines, the Petasis reaction tolerates a multifunctional scaffold, with a variety of amines and organoboronic acids as potential starting materials. Additionally, the reaction does not require anhydrous or inert conditions. As a mild, selective synthesis, the Petasis reaction is useful in generating α-amino acids, and is utilized in combinatorial chemistry and drug discovery.
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