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Şenol, O.İ., Viljava, T.-R., Krause, AOI
Şenol, O.İ., Viljava, T.-R., Krause, AOI

... Reactions of methyl heptanoate (Fluka Chemika, >99%) and methyl hexanoate (Fluka Chemika, >99%) were studied on commercial NiMo/g-Al2O3 and CoMo/g-Al2O3 hydrotreatment catalysts in either oxide or sulphided form. Additionally, heptanoic acid (Aldrich, 99%) was used to study the reactions of a potent ...
Carbohidratos
Carbohidratos

PDF - Nanyang Technological University
PDF - Nanyang Technological University

... reactions of activated carbonyl nucleophiles (such as 1,3dicarbonyls and acetyl phosphates) to oxidatively generate iminiums or their analogues.[4d] However, this approach with chiral ligands was found to be unsuccessful for reactions starting with simple ketone nucleophiles, as reported by Klussman ...
PDF document
PDF document

... recognised for a long time as valuable synthetic tools, above all in carbon-carbon bond formation, mainly through metal catalysed coupling reactions. In addition, many iodinated aromatic derivatives are used in medicine as drugs or diagnostic aids, contrasting agents, and radioactively labelled mark ...
Carbonyl The carbonyl function, C=O, exists in a number of organic
Carbonyl The carbonyl function, C=O, exists in a number of organic

... groups to form alcohols constitute a major process in organic chemical synthesis. These reagents add easily to the carbonyl group but as strong bases they can also form alphacarbanions that give aldol reactions. The aldol reactions are minimized by working at cold temperatures. The reaction is exemp ...
Synthesis of Natural Products and Related Compounds using Enyne
Synthesis of Natural Products and Related Compounds using Enyne

... and the catalytic activity is decreased, 67 was converted into 67·HCl and dienyne metathesis was carried out using ruthenium catalyst 1c. As a result, tetracyclic compounds 68a and 68b were obtained as a diastereomeric mixture in a ratio of 1 to 1. From the a-isomer 68a, erythrocarine was synthesize ...
cycloadditions with singlet oxygen
cycloadditions with singlet oxygen

... major product observed. Once formed, the two endoperoxides did not interconvert. The preferential formation of the anti cycloadduct was unique to singlet oxygen because other dienophiles such as maleic anhydride and N-phenylmaleimide proceeded to give syn products with bisdialine. Carpenter reported ...
Review on N acylation reaction
Review on N acylation reaction

6. Low valent of Vanadium catalyst in organic synthesis
6. Low valent of Vanadium catalyst in organic synthesis

... *the coordination of the phosphorus raises the reduction capability and selectivity. *the bulky reductant is liable to approach the bromide from the less hindered side Toshikazu Hirao,J. Org. Chem., 1993, 58 (23), 6529-6530 ...
DEPARTMENT OF CHEMISTRY
DEPARTMENT OF CHEMISTRY

... sampling. Current trends in the analysis of metal ions and organic pollutants in water, air and soil. Laws, and standards on environmental pollution, and abatement. Book: Skoog and Leary, "Principles of Instrumental Analysis"; Skoog, West, and Holler, “Analytical Chemistry an Introduction”; Bailey, ...
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- Iranian Journal of Science and Technology (Sciences)

... obtained from the reaction of triethylamine and chlorodiphenylphosphine was selected as the most suitable reagent and media for performing the esterification reactions. Apart from the ease of handling and preparation of this IL, the phosphine oxide formed in the reaction is taken up by the ionic liq ...
Bimolecular reactions of the chromium
Bimolecular reactions of the chromium

Microsoft Word - Open Access Repository of Indian Theses
Microsoft Word - Open Access Repository of Indian Theses

... The conjugate addition (1,4-addition or Michael addition) of nucleophiles to α,βunsaturated compounds is one of the most important new bond-forming strategies in synthetic organic chemistry. Aza-Michael addition is one of the important reactions especially for the synthesis of C-N heterocycles conta ...
Starter S-30
Starter S-30

... How many moles of NH3 would be produced? For every 1 mole of N2, 2 moles of NH3 ...
Synthesis of Low Molecular Weight Flavor Esters Using Plant
Synthesis of Low Molecular Weight Flavor Esters Using Plant

... occurs under these conditions in a predominantly organic media with only small amount of water present. Plant lipases have properties that may make them especially suitable for ester synthesis (Ncube and others 1993). The different synthesis yields can be ascribed to at least 3 factors. First, the s ...
Chiral Enolate Equivalents
Chiral Enolate Equivalents

... 2500 Boul. Université, Sherbrooke, Qc, CANADA, J1K 2R1 INTRODUCTION Enolate chemistry is a very mature subject but it was long after the enolate was recognized as a pivotal functionality for carbon-carbon bond forming processes that stereochemical control in this reaction was finally achieved. Follo ...
Preparation of Cyclic Urethanes from Amino Alcohols and Carbon
Preparation of Cyclic Urethanes from Amino Alcohols and Carbon

... viewpoints. Cyclic urethanes are produced from amino alcohols and CO2 even in the absence of catalysts, but, unfortunately, their yields are low [11,16,18]. Desirable high yields can be achieved by employing stoichiometrically consumed dehydration [12,13] or deoxygenation reagents [14,15]. However, ...
Document
Document

Unit 2 Chemical Reactions
Unit 2 Chemical Reactions

... Acetylene gas is a fuel used in welding torches, and it combines with oxygen to produce a very hot flame. Because it is an organic compound, it contains carbon. When it burns in pure oxygen, it should produce carbon dioxide. This gas is the product of complete combustion. If there is not enough oxyg ...
Chapter 8
Chapter 8

... decomposition, single-displacement, and doubledisplacement reactions. • Classify a reaction as a synthesis, decomposition, single-displacement, double-displacement, or combustion reaction. • List three kinds of synthesis reactions and six kinds of decomposition reactions. ...
Common aldehydes and ketones
Common aldehydes and ketones

... Exceptions to this rule exist, one being formaldehyde (a gas in its pure monomeric state). Thus, a solution of formaldehyde in water (formalin) is almost exclusively the hydrate, or polymers of the hydrate. Another is chloral hydrate ...
Selective Oxidation Reactions of Natural Compounds with
Selective Oxidation Reactions of Natural Compounds with

... according to literature method [51]. Hydrogen peroxide (35%), pyridine and methyltrioxorhenium are ...
DEPARTMENT OF CHEMISTRY Course Book for M.Sc. in Chemistry
DEPARTMENT OF CHEMISTRY Course Book for M.Sc. in Chemistry

... Transition metal Chemistry: Introduction: Structure of metal ligand complexes, coordination no., isomerism, thermodynamic stability, stability constant, Irving –Willium series, Chelate and macrocyclic effect Theories of bonding : VBT, CFT, d-orbital splitting in octahedral, JT-distorted octahedral, ...
template - Communications in Inorganic Synthesis
template - Communications in Inorganic Synthesis

... The oxydiacetate anion (oda, O(CH2COO)22-) is a versatile ligand having five potential oxygen donors, four from two carboxylate groups and the fifth from an ether group. It may bind to metal ions in mono-, bi-, tri- and multidentate coordination modes. A number of oda complexes with lanthanide ions ...
Lab 9 - Academic Computer Center
Lab 9 - Academic Computer Center

... The second comes from the workup of the reaction, which is normally conducted in aqueous acid. Sodium borohydride, NaBH4, is the mildest of the three hydride reagents and is easy to use in the lab, because it is soluble in water, methanol and ethanol and does not react with these solvents. Therefore ...
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Enantioselective synthesis



Enantioselective synthesis, also called chiral synthesis or asymmetric synthesis, is defined by IUPAC as: a chemical reaction (or reaction sequence) in which one or more new elements of chirality are formed in a substrate molecule and which produces the stereoisomeric (enantiomeric or diastereoisomeric) products in unequal amounts.Put more simply: it is the synthesis of a compound by a method that favors the formation of a specific enantiomer or diastereomer.Enantioselective synthesis is a key process in modern chemistry and is particularly important in the field of pharmaceuticals, as the different enantiomers or diastereomers of a molecule often have different biological activity.
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