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Titlebook: Organotitanium Reagents in Organic Synthesis; Manfred T. Reetz Book 1986 Springer-Verlag Berlin Heidelberg 1986 chirality.organic chemistr

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书目名称Organotitanium Reagents in Organic Synthesis
编辑Manfred T. Reetz
视频video
丛书名称Reactivity and Structure: Concepts in Organic Chemistry
图书封面Titlebook: Organotitanium Reagents in Organic Synthesis;  Manfred T. Reetz Book 1986 Springer-Verlag Berlin Heidelberg 1986 chirality.organic chemistr
描述Titanium has been used to perform many kinds of reactions in organic and inorganic chemistry. The present book is concerned primarily with a new development in titanium chemistry which is useful in organic synthesis. In 1979/80 it was discovered that the titanation of classical carbanions using C1TiX leads to species with reduced basicity and reactivity. This increases 3 chemo-, regio-and stereo selectivity in reactions with organic compounds such as aldehydes, ketones and alkyl halides. Many new examples have been reported in recent times. Since the nature of the ligand X at titanium can be widely varied, the electronic and steric nature of the reagents is easily controlled. This helps in predicting the stereochemical outcome of many of the C-C bond forming reactions, but the trial and error method is still necessary in other cases. One of the ultimate objectives of chemistry is to understand correlations between structure and reactivity. Although this goal has not been reached in the area of organotitanium chemistry, appreciable progress has been made. A great deal of physical and computational data of organotitanium compounds described in the current and older literature (e. g.
出版日期Book 1986
关键词chirality; organic chemistry; organic synthesis; polymer; synthesis
版次1
doihttps://doi.org/10.1007/978-3-642-70704-9
isbn_softcover978-3-642-70706-3
isbn_ebook978-3-642-70704-9Series ISSN 0341-2377
issn_series 0341-2377
copyrightSpringer-Verlag Berlin Heidelberg 1986
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Book 1986opment in titanium chemistry which is useful in organic synthesis. In 1979/80 it was discovered that the titanation of classical carbanions using C1TiX leads to species with reduced basicity and reactivity. This increases 3 chemo-, regio-and stereo selectivity in reactions with organic compounds suc
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Stereoselectivity in the Addition of Organotitanium Reagents to Carbonyl Compounds,avor of .. Methyllithium shows the opposite stereoselectivity . = 34:66), in line with the simple assumption that attack occurs at the sterically less hindered side (aryl groups are usually considered to be bulkier than methyl groups) [4].
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Synthesis and Properties of Some Simple Organotitanium Compounds,seful in understanding reactivity and selectivity in reactions with organic substrates. Low valent Ti (II) and Ti (III) shall be mentioned only on passing; the interested reader is referred to reviews [1].
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Chemoselectivity in Reactions of Organotitanium Reagents with Carbonyl Compounds,lectivity (Chapter 1). For example, the keto-aldehyde . reacts with the lithium enolate . derived from ethyl acetate to provide a ~1:1:1 mixture of aldol adducts ., ., and . in addition to some starting material . [1,2].
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978-3-642-70706-3Springer-Verlag Berlin Heidelberg 1986
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