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Benzene, amines, amino acids and polymers File
Benzene, amines, amino acids and polymers File

... STRUCTURE OF BENZENE Primary analysis revealed benzene had... an ...
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The Synthesis of Ferrocene

... name which arose because they participated in reactions similar to those of aromatic molecules. For obvious reasons complexes in which a metal atom was found between two parallel carbocyclic rings became known as "sandwich" compounds. James E. Huheey, Ellen A. Keiter and Richard L. Keiter Inorganic ...
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molecules Palladium and Organocatalysis: An Excellent Recipe for Asymmetric Synthesis

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An Epoxidation Reaction: The Epoxidation of Cholesterol to 5 ,6

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Platinum Metals Complex Catalysts for Liquid

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... amino acids during artificial peptide synthesis. Under standard conditions, it exists in the form of white crystals with a heavy, sweet odor. The low melting point of this material allows it to be melted for easy handling. It is highly soluble in dichloromethane, tetrahydrofuran, acetonitrile and di ...
Functional groups and homologous series
Functional groups and homologous series

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Using the reduced La(Co,Cu)O3 nanoperovskites as catalyst

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Synthesis and Characterization of PhCC-Ru-L-Ru

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nanyang technological university entrance examination syllabus for

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... bond in a molecule it is necessary to activate this bond (making it more reactive) as the first step, followed by its subsequent functionalization [1a]. The activation process can be achieved effectively by using transition metal catalysts and others [1c,11]. It is well−known that complexes based on ...
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Alcohols, Phenols and Ethers

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Oxidation of Benzyl Ethers to Benzoate Esters Using a Novel

... other aqueous solvent mixtures (Thottumkara and Vinod, 2002). Several pertinent observations were made from our initial oxidation studies. It was observed that mIBX tolerates a variety of functional groups during oxidation, and over-oxidation of alcohols is never observed, even when electron rich su ...
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Reaction mechanism of Coordination Complexes

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Ch-1-Alkanes and isomerism-corr

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Nuggets of Knowledge for Chapter 10 – Alkyl Halides II Chem 2310 I

< 1 ... 46 47 48 49 50 51 52 53 54 ... 148 >

Ring-closing metathesis



Ring-closing metathesis, or RCM, is a widely used variation of olefin metathesis in organic chemistry for the synthesis of various unsaturated rings via the intramolecular metathesis of two terminal alkenes, which forms the cycloalkene as the E- or Z- isomers and volatile ethylene.The most commonly synthesized ring sizes are between 5-7 atoms; however, reported syntheses include 45- up to 90- membered macroheterocycles. These reactions are metal-catalyzed and proceed through a metallacyclobutane intermediate. It was first published by Dider Villemin in 1980 describing the synthesis of an Exaltolide precursor, and later become popularized by Robert H. Grubbs and Richard R. Schrock, who shared the Nobel Prize in Chemistry, along with Yves Chauvin, in 2005 for their combined work in olefin metathesis. RCM is a favorite among organic chemists due to its synthetic utility in the formation of rings, which were previously difficult to access efficiently, and broad substrate scope. Since the only major by-product is ethylene, these reactions may also be considered atom economic, an increasingly important concern in the development of green chemistry.There are several reviews published on ring-closing metathesis.
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