Книга: Sunil T. Patel,Kirti M. Joshi and Naresh K. Prajapati «Asymmetric Oxidation»
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Производитель: "LAP Lambert Academic Publishing" This book Asymmetric Oxidation is an interesting portrait about the oxidation with some example in nature,human body&living organization. Oxidation is about manmade things Asymmeric oxidation chemistry in this book is the base of organic oxidation reactions. Chapter 1 describes the applicative organic oxidation reactions. What are the substrates, product(selective/Non-selective) and the oxidizing agents. We straight want to dicusss about the epoxide in this book. when epoxidation is invented&which process is commercialized is described. Epoxide is used with some product is given in this chapter. Chapter 2 shows how alkene is epoxidized by use of some catalyst. Chapter 3 devotes for structural study for the epoxidation methods. Chapter 4 Shows different type of asymmetric epoxidation. Chapter 5 indicates mechanistic study of electon,radical,bond making, bond breaking,weak interactions between metal&oxygen also between substrate&oxygen. The stereo-electronic factors of... ISBN:9783659287633 Издательство: "LAP Lambert Academic Publishing" (2014)
ISBN: 9783659287633 |
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См. также в других словарях:
Asymmetric synthesis — Asymmetric synthesis, also called chiral synthesis, enantioselective synthesis or stereoselective synthesis, is organic synthesis which introduces one or more new and desired elements of chirality. [GoldBookRef|title=asymmetric synthesis| file =… … Wikipedia
Asymmetric catalytic oxidation — is a technique of oxidizing various substrates to give an enantiopure product using a catalyst.Reactions*Jacobsen epoxidation of alkenes using manganese salen complex and NaOCl *Sharpless epoxidation of allyl alcohols using titanium isopropoxide … Wikipedia
Oxidation with dioxiranes — refers to the introduction of oxygen into organic molecules through the action of a dioxirane. Dioxiranes are well known for their oxidation of alkenes to epoxides; however, they are also able to oxidize other unsaturated functionality,… … Wikipedia
Oxidation of primary alcohols to carboxylic acids — The oxidation of primary alcohols to carboxylic acids is an important oxidation reaction in organic chemistry. When a primary alcohol is converted to a carboxylic acid, the terminal carbon atom increases its oxidation state by four. Oxidants able … Wikipedia
Oppenauer oxidation — Oppenauer oxidation, named after Rupert Viktor Oppenauer,[1] is a gentle method for selectively oxidizing secondary alcohols to ketones. The reaction is the opposite of Meerwein Ponndorf Verley reduction. The alcohol is oxidized with aluminium… … Wikipedia
Sharpless asymmetric dihydroxylation — (also called the Sharpless bishydroxylation) is the chemical reaction of an alkene with osmium tetroxide in the presence of a chiral quinine ligand to form a vicinal diol.[1][2][3] … Wikipedia
