Yoichi Hoshimoto 교수

Chemists no longer doubt the importance of a methodology that could activate and utilize aldehydes in organic syntheses since many products prepared from them support our daily life. Tremendous effort has been devoted to the development of these methods using main-group elements and transition metals. Thus, many organic chemists have used an activator-(aldehyde oxygen) interaction, namely, η(1) coordination, whereby a Lewis or Brønsted acid activates an aldehyde. In the field of coordination che

In the presence of a Ni(0)/NHC catalyst, an equimolar mixture of aliphatic and aryl aldehydes can be employed to selectively yield a single cross-coupled ester. This reaction can be applied to a variety of aliphatic (1°, 2°, cyc-2°, and 3°) and aryl aldehyde combinations. The reaction represents 100% atom efficiency and generates no waste. Mechanistic studies have revealed that the striking feature of the reaction is the simultaneous coordination of two aldehydes to Ni(0).

The first nickel(0)-catalyzed [2 + 2 + 1] carbonylative cycloaddition reaction of imines and alkynes or norbornene has been achieved by employing phenyl formate as a CO source. With this method, a variety of N-benzenesulfonyl, -tosyl, and -phosphoryl-substituted γ-lactams can be prepared in good to high yields.

Recently, the combination of Ni(0) and N-heterocyclic carbenes (NHCs) has been paid special attention because of its high reactivity toward bond-forming reactions and the activation of unreactive bonds. Thus, it would be very worthwhile to provide a highly reactive, easily accessible, and versatile Ni0–NHC precursor. Herein we report a one-pot, single-step, and gram-scale method for the synthesis of [(η6-arene)Ni(NHC)] complexes from commercially available Ni(cod)2 and NHC (or its salt) via hydr

Despite there being a straightforward approach for the synthesis of 1,2-dihydropyridines, the transition-metal-catalyzed [2+2+2] cycloaddition reaction of imines with alkynes has been achieved only with imines containing an N-sulfonyl or -pyridyl group. Considering the importance of 1,2-dihydropyridines as useful intermediates in the preparation of a wide range of valuable organic molecules, it would be very worthwhile to provide novel strategies to expand the scope of imines. Herein we report a

The nickel(0)-catalyzed carbonylative cycloaddition of 1,5- and 1,6-ene-imines with carbon monoxide (CO) is reported. Key to this reaction is the efficient regeneration of the catalytically active nickel(0) species from nickel carbonyl complexes such as [Ni(CO)₃ L]. A variety of tri- and tetracyclic γ-lactams were thus prepared in excellent yields with 100 % atom efficiency. Preliminary results on asymmetric derivatives promise potential in the synthesis of enantioenriched polycyclic

Recent progress on the triarylborane (BAr3)-catalyzed reductive N-alkylation of amines is briefly summarized in this Perspective. The highlighted examples are divided into two main classes, that is, the B(C6F5)3-catalyzed hydroamination of alkynes and subsequent catalytic hydrogenation, as well as the BAr3-catalyzed reductive N-alkylation of carbonyl compounds such as aldehydes, ketones, and carboxylic acids in the presence of hydrosilanes or molecular hydrogen. Key aspects on several catalytic

N-Phosphine oxide substituted imidazolylidenes (PoxIms) have been synthesized and fully characterized. These species can undergo significant changes to the spatial environment surrounding their carbene center through rotation of the phosphine oxide moiety. Either classical Lewis adducts (CLAs) or frustrated Lewis pairs (FLPs) are thus formed with B(C6 F5 )3 depending on the orientation of the phosphine oxide group. A strategy to reactivate FLPs from CLAs by exploiting molecular motions that are

An η(2)-aldehyde nickel complex was utilized as an effective activator for an organosilane in order to generate a hypervalent silicate reactant for the first time. This method was successfully applied to the highly efficient syntheses of 3-aryl-, vinyl-, and alkynyl-2,1-benzoxasiloles from benzaldehydes with aryl-, vinyl-, and alkynylsilyl groups at the ortho position. Initial mechanistic studies revealed that an intermolecular aryl transfer process was involved in the reaction mechanism. The fo

Molecular hydrogen (H₂) is one of the most important energy carriers. In the midterm future, a huge amount of H₂ will be produced from a variety of hydrocarbon sources through conversion and removal of contaminants such as CO and CO₂. However, bypassing these purification processes is desirable, given their energy consumption and environmental impact, which ultimately increases the cost of H₂. Here, we demonstrate a strategy to separate H₂ f

Direct synthesis of carboxylic-phosphinic mixed anhydrides has been achieved by treating carbon dioxide with N-phosphine oxide-substituted imidazolylidenes (PoxIms) that contain both nucleophilic carbene and electrophilic phosphorus moieties. This novel mixed anhydride was efficiently derivatized into an ester, an amide, and an unsymmetrical ketone via transformation into its corresponding imidazolium salt followed by a dual substitution reaction. The presented work used well-designed multifunct

This article discusses the concept of N-heterocyclic carbenes (NHCs) equipped with more than one functional moiety, which allows using these NHCs for multiple purposes. A pioneering example for such NHCs is N-phosphine oxide-substituted imidazolylidenes (PoxIms), and their synthesis and strategic use are highlighted. The utility of PoxIms by far exceeds the conventional use as multidentate ligands for metal complexes on account of the synergetic functions of the carbene and the N-phosphine oxide

A novel strategy for the preparation of heterobimetallic <i>N</i>-heterocyclic carbene (NHC) complexes is demonstrated using <i>N</i>-phosphine-oxide-substituted imidazolylidenes (PoxIms). In these heterobimetallic Cu/Al complexes, the Cu and Al centers can be either completely separated or brought near each other via the rotation of the <i>N</i>-phosphinoyl group in the PoxIm ligands. Triggered by this rotation, transmetalation to exchange the Cu-O^tBu and Al-C₆F<sub>5</sub

Chemisorption on organometallic-based adsorbents is crucial for the controlled separation and long-term storage of gaseous molecules. The formation of covalent bonds between the metal centers in the adsorbents and the targeted gases affects the desorption efficiency, especially when the oxidation state of the metal is low. Herein, we report a pressure-responsive nickel(0)-based system that is able to reversibly chemisorb carbon monoxide (CO) at room temperature. The use of <i>N</i>-heterocyclic

Abstract The nickel(0)‐catalyzed carbonylative cycloaddition of 1,5‐ and 1,6‐ene‐imines with carbon monoxide (CO) is reported. Key to this reaction is the efficient regeneration of the catalytically active nickel(0) species from nickel carbonyl complexes such as [Ni(CO) 3 L]. A variety of tri‐ and tetracyclic γ‐lactams were thus prepared in excellent yields with 100 % atom efficiency. Preliminary results on asymmetric derivatives promise potential in the synthesis of enantioenriched polycyclic γ