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Nonracemic Allylic Boronates through Enantiotopic-Group
Nonracemic Allylic Boronates through Enantiotopic-Group

... tertiary allylic alcohol 19 with excellent enantiomeric purity. To study the ability of this catalytic cross-coupling to deliver synthetically useful quantities of material, the reaction in Scheme 3 was undertaken. In this experiment, the alkylation of ...
Dehydration of n-propanol and methanol to produce
Dehydration of n-propanol and methanol to produce

... and methanol with catalysts that are used in transesterification. Experiments were carried out to evaluate the feasibility of promoting etherification reaction using methanol and n-propanol as model alcohols. When methanol and n-propanol are reacted together, three types of ethers can be produced; i ...
Chapter 1--Title
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Chemistry 730 - OSU Chemistry
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... To clarify distinction between stereoisomers - configuration must be specified. Stereoisomers: enantiomers and diastereomers - enantiomers- Stereoisomers that are related by a mirror-image relation (related by having nonsuperimposable mirror images) homochirally related when the enantiomers are simi ...
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... Alkyl halides are most commonly synthesized from alcohols by replacing the hydroxyl group with a halide substituent. This is an example of nucleophilic aliphatic substitution, which is part of a very important group of reactions. The overall reaction is the same, but the mechanism varies depending o ...
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Arrows - Rutgers Chemistry

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14 - Oxidation of Alcohols - Organic Chemistry at CU Boulder

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Unit 4, Lesson #3 - Patterson Science

... Keq, is called the equilibrium constant for this reaction at a specified temperature. Because Keq depends on reaction rates, and reaction rates depend on temperature, the value for Keq is different at different temperatures. The temperature must be reported along with the value of Keq. ...
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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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