DMSO-I2-Promoted Insertion of Isocyanide into the N–H Bond of Amines: Synthesis of Ureas

Metal-catalyzed insertion reactions of isocyanides into amines have been developed with the ultimate goal of synthesizing nitrogen-containing heterocycles. These routes have had problems in that isocyanides often strongly coordinate to metal catalysts, and they often undergo polymerization under these conditions.1 Because of this, there is interest in developing metal-free methods. The metal-free insertion of an […]

DMSO/I2-Catalyzed Functionalization of Cyclohexanones: Synthesis of Phenylenediamines

N,Nʹ-Diaryl-o-phenylenediamines are precursors to many N-heterocyclic carbenes and are substructures of many medicinal substances, yet there are few routes to synthesize these compounds. This makes the metal-free method recently published by the Pan group particularly attractive.1 The method described by Pan’s group is simple, uses easily-acquired starting materials, and, with the use of the DMSO/I2 catalyst, is relatively […]

Metal-, Photocatalyst, and Light-Free Alkylation of Heteroarenes and Quinones in DMSO

Methods to perform late-stage C–H alkylations are highly valued because these reactions generally must be mild and tolerated by many substrates. Because of these constraints, often the scope of such reactions is limited. This makes the new metal-free, photocatalyst-, and light-free method described by the Lee group an important advance.1 All of the reagents/reactants in […]

DMSO/I2: Simple and Green Syntheses of Imidazoles

Imidazoles are crucial building blocks for many pharmaceuticals and agrichemicals.  Trisubstituted imidazoles are particularly important. Therefore, several methods have been developed to synthesize these structural units; however, these methods generally have several drawbacks, including the need for complex and harsh reaction conditions and toxic transition metal reagents. Additionally, they sometimes produce many side products. Therefore, […]

Synthesis of Nitronaphthylamines using KOH/DMSO

Amino and nitro-substituted naphthalenes are important structural units in pharmaceutical materials. Recently, the Verma group reported the first synthesis of nitronaphthylamines through a one pot reaction that involves an aza-Henry reaction followed by an annulation.1 This synthesis uses nitromethane in KOH/DMSO. This method can be extended to incorporate acetonitrile or benzophenone in place of nitromethane (Figure […]

Visible-Light-Induced Synthesis of Vinyl Sulfones from Cinnamic Acids in DMSO

Dimethyl sulfoxide continues to be the solvent of choice for several light-induced reactions. (For other recent examples see Synthesis Corner posts from May 31, 2019, January 2, 2019, and October 1, 2018.) Recently Li and Wang demonstrated the light-induced synthesis of vinyl sulfones starting from various cinnamic acids and sodium arylsulfinates (Table 1).1 This reaction uses […]

DMSO/I2 Oxidation to Produce Heteroaromatic Aldehydes

The oxidation methods using DMSO/I2 continue to grow. (For recent examples, see Synthesis Corner posts from January 6, 2020, October 31, 2019, and October 1, 2019.) These methods generally proceed through iodine-catalyzed C–H functionalization followed by a Kornblum-type oxidation at the same site. Along these lines, recent work by Chen et al. demonstrates the first example […]

DMSO/I2-Mediated Synthesis of 3-Thiomethyl Chromones

Chromones are important structural subunits in many natural products and biologically active compounds. Therefore, methods to synthesize or functionalize this structural motif are of high interest. The Wang and Wu group recently published their work where DMSO/I2 facilitates the three-component synthesis of chromones containing a thiomethyl group at the 3-position (3 in Table 1).1 This adds to the […]

Visible-Light-Mediated Synthesis of γ-Ketoesters in DMSO

γ-Ketoesters are common synthetic building blocks. Therefore, diverse synthetic methods have been developed to prepare these compounds. Recently, the Liu group reported a visible-light-mediated method, using compact fluorescent light (CFL), where the oxidative coupling of readily available vinylarenes and bromocarboxylates, followed by a Kornblum-type oxidation in DMSO, furnishes the desired γ-ketoester (equation in Table 1, […]

Dichlorocyclopropene Activation of DMSO for Swern Type Oxidations

Oxidations of primary alcohols using activated DMSO to produce aldehydes are important reactions. Oxalyl chloride is a common activator for DMSO (Swern oxidation) and has been widely used. However, oxalyl chloride has some drawbacks in that it is volatile and toxic. Additionally, the oxalyl chloride/DMSO pair must be kept cold (less than –60 °C) to […]