Organotitanium Reagents in Organic Synthesis
Published on 1. March 1986
Book
Hardback
X, 236 pages
978-3-540-15784-7 (ISBN)
Description
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. , Ziegler-Natta type catalysts) has been reported by polymer, inorganic and theoretical chemists. It is summarized in Chapter 2 of this book, because some aspects are useful in understanding reactivity and selectivity of organo titanium compounds in organic synthesis as described in the chapters which follow.
More details
Series
Edition
1986
Language
English
Place of publication
Heidelberg
Germany
Publishing group
Springer Berlin
Target group
Professional and scholarly
Research
Illustrations
X, 236 p.
Dimensions
Height: 0 mm
Width: 0 mm
Weight
570 gr
ISBN-13
978-3-540-15784-7 (9783540157847)
DOI
10.1007/978-3-642-70704-9
Schweitzer Classification
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Manfred T. Reetz
Organotitanium Reagents in Organic Synthesis
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11/2011
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Content
1. Introduction.- 1.1 Adjustment of Carbanion-Selectivity via Titanation.- 1.2 Other Uses of Titanium in Organic Chemistry.- References.- 2. Synthesis and Properties of Some Simple Organotitanium Compounds.- 2.1 Synthesis and Stability.- 2.1.1 Historical Aspects.- 2.1.2 Mono-Aryl- and Alkyltitanium Compounds.- 2.1.3 Polyalkyl- and Aryltitanium Compounds.- 2.1.4 h5-Cyclopentadienyltitanium(IV) Compounds.- 2.2 Bond Energies.- 2.3 Bond Angles and Lengths.- 2.4 Aggregation State.- 2.5 Spectroscopic and Theoretical Aspects.- 2.5.1 Introductory Remarks.- 2.5.2 Methyltitanium Compounds.- 2.5.3 h5-Cyclopentadienyltitanium Compounds.- 2.6 Conclusions.- References.- 3. Chemoseleetivity in Reactions of Organotitanium Reagents with Carbonyl Compounds.- 3.1 Aldehyde/Ketone Differentiation.- 3.1.1 Reagents of the Type RTi(OCHMe2)3.- 3.1.2 Organotitanium Reagents Bearing Other Ligands.- 3.1.3 Titanium Ate Complexe.- 3.2 Aldehyde/Aldehyde and Ketone/Ketone Differentiation.- 3.3 Chemo- and Regioselective Additions to ?,?-Unsaturated Carbonyl Compounds.- 3.4 Aldehyde/Ester and Ketone/Ester Differentiation.- 3.5 Reactions in the Presence of Additional Functionality.- 3.6 Addition to Enolizable Ketones.- 3.7 Limitations of Organotitanium Reagents.- 3.8 Hints on How to Use Organotitanium Compounds.- 3.9 Why Does Titanation of Carbanions Increase Chemoselectivity?.- 3.10 Comparison with Other Organometallic Reagents.- 3.11 Reversal of Chemoselectivity: Chemoselective in situ Protection of Carbonyl Compounds.- 3.12 Organotitanium Reagents from Non-Organometallic Precursors 107 References.- References.- 4. Rates of Reactions.- 4.1 Kinetics of the Addition of CH3Ti(OCHMe2)3 to Carbonyl Compounds.- 4.2 Other Kinetic Studies.- References.- 5. Stereoselectivity in the Addition of Organotitanium Reagents to Carbonyl Compounds.- 5.1 Titanation of Carbanions as a Means to Control Stereoselectivity.- 5.2 Diastereofacial Selectivity.- 5.2.1 The Cram/anti-Cram Problem.- 5.2.2 Chelation-Control in Addition Reactions of Chiral Alkoxy Carbonyl Compounds.- 5.2.2.1 1,2 Asymmetric Induction.- 5.2.2.2 1,3 and 1,4 Asymmetric Induction.- 5.2.3 Non-Chelation-Controlled Additions to ?-Chiral Alkoxy Carbonyl Compounds.- 5.3 Simple Diastereoselectivity.- 5.3.1 Titanium-Mediated Aldol Additions.- 5.3.2 Aldol-Type Additions of Titanated Heterocycles.- 5.3.3 Addition of Prochiral Allylic Titanium Reagents.- 5.3.4 Addition of Prochiral Propargyl-Titanium Reagents.- 5.4 The Problem of Equatorial vs. Axial Addition to Cyclic Ketones.- 5.5 Enantioselective Additions.- 5.5.1 Reagents with Chirally Modified Ligands at Titanium.- 5.5.2 Reagents with the Center of Chirality at Titanium.- 5.5.3 Titanation of Carbanions which Contain a Chiral Auxiliary.- References.- 6. Michael Additions.- References.- 7. Substitution Reactions.- 7.1 Titanium Enolates as Nucleophiles.- 7.2 Alkyltitanium Compounds as Nucleophiles.- 7.2.1 SN1-Active Alkyl Halides and Related Alkylating Agents.- 7.2.2 Direct Geminal Dialkylation of Ketones and Aldehydes and Exhaustive Methylation of Acid Chlorides.- 7.2.3 Acetals as Alkylating Agents.- 7.2.4 Metallated N,0-Hemiacetals as Alkylating Agents.- 7.3 Other Substitution Reactions: Present and Future.- References.- 8. Wittig-type Methylenation of Carbonyl Compounds.- References.