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Introduction

  • Chapter
Organotitanium Reagents in Organic Synthesis

Part of the book series: Reactivity and Structure: Concepts in Organic Chemistry ((REACTIVITY,volume 24))

Abstract

Carbanion chemistry represents an integral part of organic synthesis [1]. Not only simple Grignard- and alkyllithium compounds are useful in C—C bond formation, but also a host of heteroatom-substituted and resonancestabilized species generated by such classical methods as halogen-metal exchange or deprotonation of CH-acidic organic compounds. Countless examples of addition reactions of carbonyl compounds (Grignard- and aldol-type), Michael additions, substitution processes involving alkyl halides or sulfonates as well as Wittig-like olefinations have been reported.

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  1. Fachbereich Chemie der Universität Marburg, D-3550, Marburg, Germany

    Professor Dr. Manfred T. Reetz

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  1. Professor Dr. Manfred T. Reetz
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© 1986 Springer-Verlag Berlin Heidelberg

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Reetz, M.T. (1986). Introduction. In: Organotitanium Reagents in Organic Synthesis. Reactivity and Structure: Concepts in Organic Chemistry, vol 24. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-70704-9_1

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  • DOI: https://doi.org/10.1007/978-3-642-70704-9_1

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-70706-3

  • Online ISBN: 978-3-642-70704-9

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