Remote C-H Bond Functionalizations. Группа авторов

Remote C-H Bond Functionalizations

tutorial resources for future generation to accomplish successive progress, is undeniably one of the best efforts to intensify the expansion of chemical synthesis.

H bond being the fundamental backbone of organic compounds, the potential of a C–H functionalization to amend a molecule overrides traditional routes on grounds of step and atom economy. This has triggered the development of various strategies with the aim to alter the physicochemical properties of specific compounds or add on molecular complexity. Irrespective of aliphatic or aromatic setup, the C

H bonds, vicinal to a functional group, are relatively easier to functionalize either by exploiting its acidity or by taking the advantage of its coordinating ability to the metal. Moving further toward distal positions, C–H functionalization is engrossed with several issues including the intrinsic inertness as well as regioselectivity due to the overabundance of multiple C

H bonds with subtle reactivity differences. Therefore, a curious quest was always followed to execute distal C–H functionalization with precise site selectivity. In its itinerary thus far, a number of elegant approaches have been conceived to install functional group at distal location with precise and predictable selectivity. In this book, an attempt is made to provide a broad overview on contemporary advancements in the field of distal C–H functionalization. Eminent researchers, who are known for their significant contributions in distinguished research areas, have penned down their collective efforts to outline a coherent and comprehensive discussion about different strategies for distal C–H functionalization.

Chapter 2 introduces to the realm of directing group (DG) assisted distal arene meta‐functionalization. Precise control on regioselectivity is one of the most important aspects in arene C–H functionalization. Arenes bearing heteroatom containing functionality, which is famously known as directing group (DG), were extensively exploited for proximal ortho‐C–H activation. Extending such DG‐assisted distal meta‐functionalization strategy required proper template engineering that would ensure the meta‐selective C–H activation. In this context, Yu and coworkers disclosed a “U”‐shaped template for meta‐selective alkenylation. Thereafter, Yu, Maiti, Tan, Li, and others embarked on exploring the scope of meta‐functionalizations employing several templates. Gao and Li have collectively penned down in delineating a monograph on recent development of transition metal‐catalyzed, template assisted distal meta‐C–H functionalization.

Chapter 3 deals with the involvement of the Catellani reaction for distal functionalization of (pseudo)halo arenes. Transition metal‐catalyzed cross‐coupling reactions have revolutionized the art of modern synthesis. While aryl halides or pseudohalides produced ipso‐functionalized compounds, a new class of reactivity of aryl (pseudo)halide was developed by Catellani utilizing the combination of strained bicyclic olefin, norbornene (NBE), and palladium. A phenylnorbornylpalladium(II) (PNP) dimeric Pd‐catalyst was successfully employed to furnish o,o′‐disubstituted vinylarenes starting from aryl iodides, alkyl iodide, and olefin in a regioselective manner. This Pd–NBE cooperative catalysis was expanded further for a diverse class of substrates including NH‐indoles and NH‐pyrroles, arenes bearing directing group (DG), and arylboron compounds by several eminent scientists. Several electrophiles were utilized for ortho‐functionalization, and various nucleophiles were used as terminating reagent for ipso‐functionalization. In Chapter 3, Juntao Ye and Mark Lautens have provided a vivid description about the development of arene C–H functionalization relying on Pd–NBE catalysis. The discussion was initially focused on the processes initiated with Pd(0) and subsequent discussion was made on the protocols initiated with Pd(II). However, a large part of Chapter 3 was devoted in portraying synthetic applicability of the Pd–NBE cooperative catalysis.

The seminal work by Catellani on di‐functionalization of aryl (pseudo)halides evolved in 1997. In later years, enormous efforts have been devoted in expanding the scope of this Pd–NBE cooperative catalysis in a relayed C–H activation process. In this context, Dong and Yu independently pioneered a directing group assisted meta‐C–H functionalization utilizing the concept of Catellani reaction. An ortho‐directing group was employed for initial ortho‐C–H activation and subsequent palladium relay was realized in presence of NBE to accomplish meta‐selective arene‐C–H functionalizations. While the directing group (DG) assisted C–H functionalization was extensively studied for ortho‐functionalization, aforementioned seminal reports opened up a new horizon in distal meta‐C–H functionalization. Cheng and Zhou discussed about the recent advancements on directing group assisted meta‐selective functionalization of arenes relying on NBE mediated Catellani type reaction. A detailed discussion was made on various functionalizations including alkylation, arylation, alkynylation, chlorination, and amination, which were achieved by anchoring different ortho‐directing groups such as amides, amines, pyridine, or even free carboxylic acid.

In Chapter 5, a comprehensive summary on ruthenium catalyzed distal meta‐ and para‐C–H functionalization was provided by Ackermann and coworkers. In last decades a number of handful synthetic protocols were developed to accomplish remote arene C–H functionalization by Ru‐catalysis. Ru‐catalyzed ortho‐C–H ruthenation and subsequent ortho‐functionalization were known in literature over few decades. In a sharp contrast, a unique catalytic reactivity to furnish meta‐functionalized product from such ortho‐ruthenated arenes was first observed by Frost and Ackermann in 2011 and 2013, respectively. In later years, Ackermann, Frost, Greaney, Zhang, and others successfully demonstrated a number of useful meta‐functionalization methods relying on similar strategy. Ru‐catalyzed para‐selective functionalization was also included in Chapter 5 to retrospect the entire spectrum of Ru‐catalyzed remote C–H functionalization.

While Chapters 2–5 of this book were focused on discussing various approaches for distal arene C(sp²)–H functionalization based on directing group assisted protocols, Catellani reactions, or via arene cyclo‐ruthenation methods, in Chapter 6 Phipps and coworkers devoted their efforts in summarizing a complementary strategy for remote arene functionalization harnessing the non‐covalent interactions. Although non‐covalent interactions are prevalent in enzymatic reactions but translating such interaction in regioselective functionalization of small molecule in synthetic scale is rare. Despite the several challenges associated in controlling the site selectivity of arene functionalization, in recent years a number of elegant methods were developed by Smith, Kanai, Phipps, Chattopadhyay, and others. Phipps and his co‐authors illuminated about the emergence of non‐covalent interaction in distal arene‐C–H functionalization in Chapter 6.

Although use of directing group, transient mediator or non‐covalent interactions have been popularized in recent years to harness the regioselective transformation of arenes. However, transition metal‐catalyzed functionalization governed by the steric and/or electronic factors was cultivated over the century to mitigate the issues pertaining to the site‐selectivity. Intrinsic biasness derived from the substituted functionality present in arenes or heteroarenes is considered to be the key component in defining the selectivity. While such strategy, precludes preinstallation of directing group or circumvent the complicated catalytic path involved in NBE mediated process, but were largely limited by the nature of substrate as well as usage of excess

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