Regioselective B(3)–H bond activation based on an o-carboranyl dithiocarboxylate ligand and its derivatives

2021 ◽  
Author(s):  
Run-Ze Yuan ◽  
Peng-Fei Cui ◽  
Shu-Ting Guo ◽  
Guo-Xin Jin
Keyword(s):  
Bond Activation ◽  
Directing Group ◽  
Activated Complex

Using methyldithiocarboxyl as the directing group, together with [Cp*IrCl2]2, selective B(3)–H activation occurs at o-carborane. A series of substitution complexes have been prepared from the B(3)–H activated complex.

Imine as a Linchpin Approach for Distal C(sp2)–H Functionalization

2020 ◽  
Author(s):  
Sukdev Bag ◽  
Sadhan Jana ◽  
Sukumar Pradhan ◽  
Suman Bhowmick ◽  
Nupur Goswami ◽  
...  
Keyword(s):  
Organic Molecules ◽  
Bond Activation ◽  
Bond Formation ◽  
Ancillary Ligand ◽  
Significant Challenge ◽  
Site Selectivity ◽  
Directing Group ◽  
Covalently Linked ◽  
Complex Organic ◽  
Post Functionalization

<p>Despite the widespread applications of C–H functionalization, controlling site selectivity remains a significant challenge. Covalently attached directing group (DG) served as an ancillary ligand to ensure proximal <i>ortho</i>-, distal <i>meta</i>- and <i>para</i>-C-H functionalization over the last two decades. These covalently linked DGs necessitate two extra steps for a single C–H functionalization: introduction of DG prior to C–H activation and removal of DG post-functionalization. We introduce here a transient directing group for distal C(<i>sp<sup>2</sup></i>)-H functionalization <i>via</i> reversible imine formation. By overruling facile proximal C-H bond activation by imine-<i>N</i> atom, a suitably designed pyrimidine-based transient directing group (TDG) successfully delivered selective distal C-C bond formation. Application of this transient directing group strategy for streamlining the synthesis of complex organic molecules without any necessary pre-functionalization at the distal position has been explored.</p>

scholarly journals Palladium-Catalysed C–F Alumination of Fluorobenzenes: Mechanistic Diversity and Origin of Selectivity

2020 ◽  
Author(s):  
Feriel Rekhroukh ◽  
Wenyi Chen ◽  
Ryan Brown ◽  
Andrew J. P. White ◽  
Mark Crimmin
Keyword(s):  
Dft Calculations ◽  
Bond Activation ◽  
Oxidative Addition ◽  
Fluorine Content ◽  
Model Potential ◽  
Heterometallic Complex ◽  
Experimental Support ◽  
Highly Active ◽  
Reaction Proceeds ◽  
Directing Group

A palladium pre-catalyst, [Pd(PCy<sub>3</sub>)<sub>2</sub>] is reported for the efficient and selective C–F alumination of fluorobenzenes with the aluminium(I) reagent [{(ArNCMe)<sub>2</sub>CH}Al] (<b>1</b>, Ar = 2,6-di-iso-propylphenyl). The catalytic protocol results in the transformation of sp<sup>2</sup> C–F bonds to sp<sup>2</sup> C–Al bonds and provides a route into reactive organoaluminium complexes (<b>2a-h</b>) from fluorocarbons. The catalyst is highly active. Reactions proceed within 5 minutes at 25 ºC (and at appreciable rates at even –50 ºC) and the scope includes low-fluorine-content substrates such as fluorobenzene, difluorobenzenes and trifluorobenzenes. The reaction proceeds with complete chemoselectivity (C–F vs C–H) and high regioselectivities ( >90% for C–F bonds adjacent to the most acidic C–H sites). The heterometallic complex [Pd(PCy<sub>3</sub>)(<b>1</b>)<sub>2</sub>] was shown to be catalytically competent. Catalytic C–F alumination proceeds with a KIE of 1.1–1.3. DFT calculations have been used to model potential mechanisms for C–F bond activation. These calculations suggest that two competing mechanisms may be in operation. Pathway 1 involves a ligand-assisted oxidative addition to [Pd(<b>1</b>)<sub>2</sub>] and leads directly to the product. Pathway 2 involves a stepwise C–H to C–F functionalisation mechanism in which the C–H bond is broken and reformed along the reaction coordinate, allowing it to act as a directing group for the adjacent C–F site. This second mechanism explains the experimentally observed regioselectivity. Experimental support for this C–H activation playing a key role in C–F alumination was obtained by employing [{(MesNCMe)<sub>2</sub>CH}AlH<sub>2</sub>] (<b>3</b>, Mes = 2,4,6-trimethylphenyl) as a reagent in place of 1. In this instance, the kinetic C–H alumination intermediate could be isolated. Under catalytic conditions this intermediate converts to the thermodynamic C–F alumination product.

Pd-Mediated γ-C(sp3)–H Bond Activation in Ammonia–Ugi 4-CR Adducts by Using Picolinamide as Directing Group

2019 ◽  
Vol 84 (20) ◽  
pp. 12809-12834 ◽  
Author(s):  
Diego Alemán-Ponce de León ◽  
Anahí C. Sánchez-Chávez ◽  
Luis A. Polindara-García
Keyword(s):  
Bond Activation ◽  
Directing Group

Direct C(sp3)–H Activation of Carboxylic Acids

Synthesis ◽  
2019 ◽  
Vol 52 (04) ◽  
pp. 479-488 ◽  
Author(s):  
Alexander Uttry ◽  
Manuel van Gemmeren
Keyword(s):  
Carboxylic Acid ◽  
General Solution ◽  
Carboxylic Acids ◽  
Bond Activation ◽  
Acid Moiety ◽  
Group Approach ◽  
Research Fields ◽  
Directing Group ◽  
Aliphatic Carboxylic Acids

Carboxylic acids are important in a variety of research fields and applications. As a result, substantial efforts have been directed towards the C–H functionalization of such compounds. While the use of the carboxylic acid moiety as a native directing group for C(sp2)–H functionalization reactions is well established, as yet there is no general solution for the C(sp3)–H activation of aliphatic carboxylic acids and most endeavors have instead relied on the introduction of stronger directing groups. Recently however, novel ligands, tools, and strategies have emerged, which enable the use of free aliphatic carboxylic acids in C–H-activation-based transformations.1 Introduction2 Challenges in the C(sp3)–H Bond Activation of Carboxylic Acids3 The Lactonization of Aliphatic Carboxylic Acids4 The Directing Group Approach5 The Direct C–H Arylation of Aliphatic Carboxylic Acids6 The Direct C–H Olefination of Aliphatic Carboxylic Acids7 The Direct C–H Acetoxylation of Aliphatic Carboxylic Acids8 Summary

Carbon Dioxide-Driven Palladium-Catalyzed C–H Activation of Amines: A Unified Approach for the Arylation of Aliphatic and Aromatic Primary and Secondary Amines

Synlett ◽  
2019 ◽  
Vol 30 (05) ◽  
pp. 519-524 ◽  
Author(s):  
Michael Young ◽  
Mohit Kapoor ◽  
Pratibha Chand-Thakuri ◽  
Justin Maxwell ◽  
Daniel Liu ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Bond Activation ◽  
Secondary Amines ◽  
Activation Process ◽  
Unified Approach ◽  
Benzylic Amines ◽  
Palladium Catalyzed ◽  
Group A ◽  
Directing Group ◽  
Site Selective

Amines are an important class of compounds in organic chemistry and serve as an important motif in various industries, including pharmaceuticals, agrochemicals, and biotechnology. Several methods have been developed for the C–H functionalization of amines using various directing groups, but functionalization of free amines remains a challenge. Here, we discuss our recently developed carbon dioxide driven highly site-selective γ-arylation of alkyl- and benzylic amines via a palladium-catalyzed C–H bond-activation process. By using carbon dioxide as an inexpensive, sustainable, and transient directing group, a wide variety of amines were arylated at either γ-sp3 or sp2 carbon–hydrogen bonds with high selectivity based on substrate and conditions. This newly developed strategy provides straightforward access to important scaffolds in organic and medicinal chemistry without the need for any expensive directing groups.1 Introduction2 C(sp3)–H Arylation of Aliphatic Amines3 C(sp2)–H Arylation of Benzylamines4 Mechanistic Questions5 Future Outlook

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