Nolan / Cazin Science of Synthesis: N-Heterocyclic Carbenes in Catalytic Organic Synthesis Vol. 1

1. Auflage 2017
ISBN: 978-3-13-201331-5
Verlag: Thieme
Format: EPUB
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)

E-Book, Englisch, 548 Seiten, ePub

The field of N-heterocyclic carbenes, whether in transition-metal catalysis or organocatalysis, is rapidly evolving towards applications, but is also still very active on the catalyst development front. Significant advances have been made over the past two decades and the development of these reactions has dramatically improved the efficiency of organic synthesis. N-Heterocyclic carbene based catalysts are now widely applied in the area of synthesis of both natural products and therapeutic agents. presents the most commonly used and significant metal- or non-metal-catalyzed reactions for modern organic synthesis. The basic principles and current state-of-the-art of the methods are covered. Scope, limitations, and mechanism of these reactions are discussed and key experimental procedures are included. Typical examples of target synthesis are often provided to show the utility and inspire further applications.

Autoren/Hrsg.

Nolan, Steven

Cazin, Catherine

Fachgebiete

• Naturwissenschaften Chemie Physikalische Chemie Chemische Reaktionen, Katalyse
• Naturwissenschaften Chemie Organische Chemie

Inhaltsverzeichnis

1.1 Introduction to N-Heterocyclic Carbenes
1.1.1 Historic Perspectives on Carbenes
1.1.2 Types of N-Heterocyclic Carbenes
1.1.3 Synthesis of N-Heterocyclic Carbenes and Their Precursors
1.1.4 Synthesis of N-Heterocyclic Carbene Complexes
1.1.5 Quantifying Steric and Electronic Properties of N-Heterocyclic Carbenes
1.2 Cross Coupling
1.2.1 Suzuki–Miyaura Coupling
1.2.2 Cross-Coupling Reactions Other Than Suzuki–Miyaura Coupling
1.2.3 The Buchwald–Hartwig Reaction
1.2.4 C—O, C—S, and C—B Bond Formation
1.3 C—H Bond Functionalization
1.4 Addition Reactions
1.4.1 Hydrogenation
1.4.2 Transfer Hydrogenation
1.4.3 Hydrosilylation
1.4.4 Catalytic Boron Addition Reactions
1.4.5 Hydroamination
1.4.6 Hydrothiolation, Hydroalkoxylation, and Hydroaryloxylation
1.4.7 Hydration
1.4.8 Hydroarylation
1.4.9 Chloroacylation and Chloroalkoxycarbonylation of Alkynes
1.4.10 Hydroformylation
1.4.11 Hydroaminomethylation

Leseproben

Abstracts

1.1.1 Historic Perspectives on Carbenes

This chapter provides a brief overview of the historical development of N-heterocyclic carbenes, from inception to isolation of the first stable aminocarbene, followed by the early applications of N-heterocyclic carbene–metal complexes as catalysts.

Keywords: N-heterocyclic carbenes • stable carbenes • metal–carbene complexes • ligands • catalysts

1.1.2 Types of N-Heterocyclic Carbenes

This chapter discusses the different types of N-heterocyclic carbenes (NHCs) and is organized according to ring size. The terminology for describing NHCs as normal or abnormal (mesoionic) and remote or nonremote is outlined. The pertinent properties of these different NHCs are compiled, in particular the 13C NMR spectroscopic and crystallographic parameters, as well as steric and electronic effects, which provides insights into the donor properties of the various classes of NHCs.

Keywords: N-heterocyclic carbenes • normal carbenes • abnormal carbenes • mesoionic • remote carbenes • nonremote carbenes • imidazolylidenes • triazolylidenes • pyrazolylidenes • cyclic alkyl (amino) carbenes • pyrimidylidenes • pyridylidenes

1.1.3 Synthesis of N-Heterocyclic Carbenes and Their Precursors

An overview of common methodologies for the preparation of free N-heterocyclic carbenes (NHCs) and their respective precursors is given. In addition to classical five-membered NHCs, examples of less-explored non-classical NHCs, including mesoionic and ring-expanded species, are also described. Experimental procedures reported in the primary literature are included for selected key compounds.

Keywords: N-heterocyclic carbenes • carbene dimers • carbene precursors • azolium salts • cyclic thioureas

1.1.4 Synthesis of N-Heterocyclic Carbene Complexes

This chapter describes the main synthetic pathways to access N-heterocyclic carbene–metal complexes. Routes covered include the complexation of free carbenes, metal-induced decomposition of carbene adducts, in situ generation of carbenes in the presence of metals, transmetalation, and templated synthesis from isocyanides.

Keywords: N-heterocyclic carbenes • carbenes • complexes • heterocycles • deprotonation • transmetalation • isocyanides • template synthesis

1.1.5 Quantifying Steric and Electronic Properties of N-Heterocyclic Carbenes

This chapter gives an overview of the most-used methods to evaluate the steric and electronic properties of N-heterocyclic carbenes (NHCs). Quantification of these properties allows for a straightforward and quantitative comparison between different NHCs, allowing for a more enlightened selection of the appropriate carbene for any given application.

Keywords: buried volume • density functional theory • electronic properties • N-hetero-cyclic carbenes • NMR methods • paramagnetic shielding • steric maps • steric properties

1.2.1 Suzuki–Miyaura Coupling

The Suzuki–Miyaura reaction of an organoboronic acid (usually an arylboronic acid) with an organo halide (typically an aryl halide) to generate a new C-C bond is one of the most valuable methods for C–C bond formation. Since the ascension of N-heterocyclic carbenes (NHCs) to occupy the position of key ligands in the repertoire of synthetic organometallic chemists, metal complexes based on these ligands have become important as catalysts for the Suzuki–Miyaura reaction. Most metal–NHC complexes used for Suzuki–Miyaura coupling are based on palladium, but an increasingly important contribution is being played by nickel-based complexes. This chapter reviews the state of the art of Suzuki–Miyaura coupling reactions catalyzed by metal–NHC complexes, with a focus on systems with broad applicability, and especially those that can be applied to “difficult” reactions such as the coupling of aryl chlorides or sterically hindered substrates. The relatively undeveloped fields of asymmetric Suzuki–Miyaura reactions and Suzuki–Miyaura reactions in water, both catalyzed by metal–NHC complexes, are also covered.

Keywords: Suzuki–Miyaura coupling • N-heterocyclic carbenes • palladium catalysis • nickel catalysis • biaryls • aryl halides • boronic acids • asymmetric synthesis • aqueous media

1.2.2 Cross-Coupling Reactions Other Than Suzuki–Miyaura Coupling

Cross coupling between a main-group organometallic nucleophile and an organic electrophile is one of the most powerful C-C bond-forming reactions in modern organic synthesis. Various palladium–N-heterocyclic carbene (NHC) complexes have been utilized in a wide range of cross-coupling reactions. The palladium–NHC systems outperform the classical palladium–phosphine catalysts in many cases, and they have solved several longstanding limitations of the classical cross-coupling protocols. This chapter covers cross couplings mediated by palladium–NHC complexes in which the nucleophile is an organomagnesium (Kumada–Tamao–Corriu coupling), an organozinc (Negishi coupling), an organotin (Stille coupling), an organosilicon (Hiyama coupling), or an organolithium, as well as Sonogashira-type couplings of alkynes.

Keywords: cross coupling • N-heterocyclic carbenes • palladium catalysis • organomagnesium • Kumada–Tamao–Corriu coupling • organozinc • Negishi coupling • organotin • Stille coupling • organosilicon • Hiyama coupling • organolithium • Sonogashira coupling

1.2.3 The Buchwald–Hartwig Reaction

This chapter covers the use of N-heterocyclic carbenes as ligands in the Buchwald–Hartwig reaction. The most efficient and convenient palladium- and nickel-based catalytic systems able to promote the C-N bond formation between various amines and (het) aryl halides or pseudohalides are reviewed.

Keywords: N-heterocyclic carbenes • palladium • nickel • C-N bond formation • Buchwald–Hartwig coupling • aryl halides • hetaryl halides • pseudohalides • trifluoromethanesulfonates • 4-toluenesulfonates • pivalates • phosphates • carbamates • sulfamates • amines

1.2.4 C-O, C-S, and C-B Bond Formation

This chapter describes the formation of C-O, C-S, and C-B bonds mediated by N-hetero-cyclic carbene based transition-metal catalysts. These reactions represent efficient and economical methods to prepare aryl ethers, phenols, sulfides (thioethers), aryl sulfoxides, and aryl boronates, all of which are important as synthetic intermediates or target compounds in natural product and materials chemistry. The transformations can be mediated by a range of metals including palladium, copper, nickel, and zinc, and the chapter is arranged accordingly.

Keywords: N-heterocyclic carbenes • C-O bond formation • C-S bond formation • C-B bond formation • ethers • phenols • sulfides • sulfoxides • boronates • aryl halides • thiols • cross coupling • palladium • copper • nickel • zinc

1.3 C-H Bond Functionalization

This chapter deals with C-H bond functionalization catalyzed by N-heterocyclic carbene transition-metal complexes. The C-H bond functionalizations have been classified with respect to the hybridization of the carbon atom and the reaction type.

Keywords: C-H bonds • metal–carbene complexes • ligands • imidazoles • imidazolylidenes • N-heterocyclic carbenes

1.4.1 Hydrogenation

From the viewpoint of atom economy and cost efficiency, hydrogenation is an ideal way to reduce various multiple bonds. In this chapter, some methods are described for the hydrogenation of alkenes, alkynes, carbonyls and related compounds, and (het) arenes using homogeneous metal–N-heterocyclic carbene (NHC) catalysts. Moreover, this section also covers enantioselective hydrogenations in which chiral NHCs are employed as ligands.

Keywords: hydrogenation • partial hydrogenation • asymmetric hydrogenation • transition-metal catalysts • carbene ligands • alkenes • alkynes • ketones • arenes • hetarenes • heterocycles • N-heterocyclic carbenes

1.4.2 Transfer Hydrogenation

The chapter describes the use of N-heterocyclic carbene (NHC) complexes of -block...