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Nomenclature
Nomenclature

... • Alkenes are soluble in organic solvents and insoluble in water. • The C—C single bond between an alkyl group and one of the double bond carbons of an alkene is slightly polar. ...


... Significance: The synthesis of isochromans 3 from tertiary alcohols 1 and alkenes 2 via a palladium-catalyzed hydroxyl-directed C–H olefination– intramolecular oxidative cyclization sequence is described. Optimization of the reaction conditions showed that the amino acid ligand shown is critical for ...
Chapter 7 Alkenes and Alkynes I
Chapter 7 Alkenes and Alkynes I

... Zaitzev’s Rule: when two different alkene products are possible in an elimination, the most highly substituted (most stable) alkene will be the major product ...
Hydrogenation of fatty acid methyl ester to fatty alcohol
Hydrogenation of fatty acid methyl ester to fatty alcohol

... seriously brought a large equipment investment, high operating costs and low security. This above explains the efforts made to arrive at low-pressure processes and low hydrogen-to-ester molar feed ratios. The favorable solvent and transport properties of supercritical fluids make them an adequate me ...
Organic Dyes as Photoredox Catalysts
Organic Dyes as Photoredox Catalysts

... The Nicewicz group recently showed that Mes–Acr+ and derivatives catalyze the direct C–H amination of electron rich arenes with nitrogen heterocyclic nucleophiles.5 The value of this method in drug design and natural product synthesis was demonstrated in the late stage derivatization of biologically ...
Palladium Nanoparticles Entrapped in Aluminum Hydroxide: Dual
Palladium Nanoparticles Entrapped in Aluminum Hydroxide: Dual

... the oxidation of 1-(4-methoxyphenyl)ethanol was completed within 1 h by 0.2 mol % Pd. A notable exception was 1-(4chlorophenyl)-ethanol; 4-chloroacetophenone was obtained in only 88% yield even after 24 h at 100 °C by 2 mol % Pd in TFT. Aromatic alcohols were oxidized faster than aliphatic ones, and ...
Conjugate (1,4
Conjugate (1,4

... steric hindrance results in predominantly one conformation ...
Synthesis_of_Organometallic_Compounds
Synthesis_of_Organometallic_Compounds

... A coordinatively unsaturated 16eruthenium(0) complex • Reduction of RuCl2(CO)2(PtBu2Me)2 with magnesium affords an isolable 16e ruthenium(0) complex Ru(CO)2(PtBu2Me)2. • Highly reactive toward hydrogen, acetylenes and phosphines to give coordinatively saturated complexes. ...
Presented by Arianne Hunter
Presented by Arianne Hunter

... variety of TPCP ligands and found the optimal catalyst was Rh2[R-3,5-di(p-tBuC6H4)TPCP]4  Provided the highest selectivity for secondary C–H functionalization and gave the best d.r. and e.e. ...
Lecture #
Lecture #

... Chemistry 335 List of topics/study guide. This is a list of topics we will be covering to help you in preparation for exams. Topics from Clayden are indicated clearly by chapter and page numbers where necessary. Topics NOT from Clayden are listed in italics. PLTL topics are in CAPS. This document wi ...
Industriel katalys
Industriel katalys

... Catalysis: definition, classification with examples, selectivity issues a) Homogeneous and heterogeneous catalysis b) Gas phase-, liquid phase-, biphasic catalysis, phase-transfer catalysis c) Metal catalysis, biocatalysis, organocatalysis Safety issues: risk and safety analysis, oxygen balance II. ...
Organometallic Chemistry
Organometallic Chemistry

... Vitamin B-12 is the name for a class of chemically-related compounds, all of which have vitamin activity. It is structurally the most complicated vitamin. A common synthetic form of the vitamin, cyanocobalamin (R = CN), does not occur in nature, but is used in many pharmaceuticals, supplements and a ...
Review Chapter 19
Review Chapter 19

... Catalytic Hydrogenation The conversion of p-bonds to s-bonds is a highly useful synthetic procedure where H2 is added across the p-bond. Although this conversion is exothermic, a catalyst is required to disrupt the di-hydrogen bond. By increasing hydrogen pressure, reaction temperature and the ...
Study_guide_2010-01
Study_guide_2010-01

... Chemistry 335 List of topics/study guide. This is a list of topics we will be covering to help you in preparation for exams. Topics from Clayden are indicated clearly by chapter and page numbers where necessary. Topics NOT from Clayden are listed in italics. PLTL topics are in CAPS. This document wi ...
Microsoft Word - Open Access Repository of Indian Theses
Microsoft Word - Open Access Repository of Indian Theses

... essential for high-affinity binding to the human NK1 (hNK1) receptor. Due to its potent biological activity, compound 42 is a good synthetic target for an organic chemist. Considering the pharmacological importance, various methods have been developed to access compound 42. These include introductio ...
Summary
Summary

... uptake of hydrogen. Furthermore, the majority of the reported metal-organic frameworks are based on transition metal carboxylate or tetrazolate systems. These studies have not yielded any materials which meet the DoE standard. The pyrazole ligand system offers many of the same advantages as the curr ...
PowerPoint 프레젠테이션
PowerPoint 프레젠테이션

... 1928–, b. Methuen, Mass., grad. Massachusetts Institute of Technology (B.S. 1948, Ph.D. 1951). In 1990, he was awarded the Nobel Prize in Chemistry. ...
• Pergamon
• Pergamon

... MetaHoporphyrins have been used extensively as models for studying cytochrome P-450 monooxygenase activity.! Although these catalysts are known to carry out many useful reactions such as alkene epoxidation and hydrocarbon oxidation, their utility in organic synthesis has been limited. Recently we re ...
Lecture 6
Lecture 6

... ligand The reverse reaction is called a β-elimination β elimination and is favored in the presence of an empty metal orbital cis to the alkyl ligand ...
Toluenediamine
Toluenediamine

... and are unstable under conditions of continuous operation. To improve the process selectivity, various additives are often introduced into the reaction medium, this resulting in considerable outlay for purification of the target product. All these shortcomings have been overcome in a new universal t ...
Stereoselective reactions of the carbonyl group
Stereoselective reactions of the carbonyl group

... • A variety of chiral Lewis acids can be used to activate the carbonyl group • These can result in fairly spectacular allylation reactions (higher ee than this example) • A problem frequently arises with crotylation • Often the reactions proceed with poor diastereoselectivity favouring either the sy ...
Organic Synthesis Part 2
Organic Synthesis Part 2

... end of the bond, and that less hindered olefins react quicker. We can use this to make di and monoorganoboranes, which can be used as more selective borane equivalents (and see also aspects of asymmetric induction!). C-B to C-H bond cleavage is achieved by heating with carboxylic acids; C-C bond for ...
Nexera UC Scouting - Shimadzu Europa GmbH
Nexera UC Scouting - Shimadzu Europa GmbH

... safer drugs, therapeutics and diagnostics. During API (active pharmaceutical ingredient) development, drug stereoisomerism is recognized as an issue having clinical and regulatory implications. Enantiomers have essentially identical physical and chemical properties, while potentially showing large d ...
Study guide/lecture topics
Study guide/lecture topics

... Chemistry 335 List of topics/study guide. This is a list of topics we will be covering to help you in preparation for exams. Topics from Clayden are indicated clearly by chapter and page numbers where necessary. Topics NOT from Clayden are listed in italics. PLTL topics are in CAPS. This document wi ...
Chapter 7 Alkenes and Alkynes I
Chapter 7 Alkenes and Alkynes I

... Bulky Base Bulky bases such as potassium tert-butoxide have difficulty removing sterically hindered hydrogens and generally only react with more accessible hydrogens (e.g. primary hydrogens) ...
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Asymmetric hydrogenation



Asymmetric hydrogenation is a chemical reaction that adds two atoms of hydrogen preferentially to one of two faces of an unsaturated substrate molecule, such as an alkene or ketone. The selectivity derives from the manner that the substrate binds to the chiral catalysts. In jargon, this binding transmits spatial information (what chemists refer to as chirality) from the catalyst to the target, favoring the product as a single enantiomer. This enzyme-like selectivity is particularly applied to bioactive products such as pharmaceutical agents and agrochemicals.
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