Rediscovering Sulfinylamines as Reagents for Organic Synthesis

Sulfinylamines (R−N=S=O), monoaza analogues of sulfur dioxide, have been known for well over a century, and their reactivity as sulfur electrophiles and in Diels-Alder reactions is well-established. However, they have only rarely been used in organic synthesis in recent decades despite the increasing prominence of compounds containing N=S=O functionality, such as sulfoximines and sulfonimidamides. This Minireview aims to bring wider visibility to the unique chemistry enabled by this class of compounds. We focus on advances from the last 10 years, including the first examples of their use in the one-pot syntheses of sulfoximines and sulfonimidamides. Also covered are the reactions of sulfinylamines with carbon-centred radicals, their use for formation of heterocycles through cycloadditions, and catalytic enantioselective allylic oxidation of alkenes via a hetero-ene reaction. These examples highlight the different reactivity modes of sulfinylamines and their underappreciated potential for forming molecules which contain high- or low-valent sulfur, or even no sulfur at all.     

Polymers as Reagents in Organic Synthesis

Polymeric reagents offer a range of unique advantages. Intramolecular reactions, such as the cyclization of peptides or Dieckmann cyclizations, can be brought about by attaching the reactive molecules at remote points along a polymer chain. In contrast, if the reactive molecules are anchored in close proximity on a polymeric support then intermolecular reactions occur, as demonstrated for a ketone synthesis. Apart from such proximity effects, cooperative effects can also be exploited, e.g. in the formation of a 2:1 complex of a crown ether and an alkali metal ion. The hydrolysis of an ester with polyvinylimidazole provides a detailed illustration of hydrophobic interactions. The simple separation of polymer-bound and low-molecular compounds by filtration is another significant advantage.     

Doped Sol-Gel Materials as Heterogeneous Reagents for Organic Synthesis

We advance the use of reactive doped sol-gel materials as heterogeneous reagents for organic-chemistry synthesis. Three approaches were demonstrated with SiO₂-based materials: Direct physical entrapment of the organic reagent; in-situ generation of an inorganic reagent within the matrix; and covalent attachment of the reagent to the matrix. With the first, entrapped p-toluenesulfonic acid facilitated the 100% yield esterification of benzoic acid with 1-pentanol, and the 100% dehydration of 1-tetralol to 1,2-dihydronaphthalene; with the second approach, a sol-gel oxidant, SiO₂/MnO₂ was used to convert benzyl alcohol to benzaldehyde and 1-tetralol to 1-tetralone; and with the third, anchored propylamine facilitated dehydrobromination reactions resulting in double-bond formation. Several other reactions with these reagents are described, and their reactivities analyzed.     

钐试剂在有机合成中的应用

本文综述了钐试剂在有机合成中的应用,包括还原反应,碳-碳键形成反应以及催化作用。     

Applications of Polymeric Reagents in Organic Synthesis

Summary. Polymer supported reagents have found many applications in recent years. Scientists in research laboratories of agrochemical and pharmaceutical industries now routinely utilize these compounds to prepare ensembles of small organic molecules for screening. This review is aimed to highlight some of the most important applications of these promising materials in organic synthesis. Furthermore, an extensive listing of polymeric reagents that were recently used in organic synthesis is included.     

Applications of Polymeric Reagents in Organic Synthesis

Polymer supported reagents have found many applications in recent years. Scientists in research laboratories of agrochemical and pharmaceutical industries now routinely utilize these compounds to prepare ensembles of small organic molecules for screening. This review is aimed to highlight some of the most important applications of these promising materials in organic synthesis. Furthermore, an extensive listing of polymeric reagents that were recently used in organic synthesis is included.     

Solid‐Phase Organic Synthesis of Aryl Vinyl Ethers Using Sulfone‐Linking Strategy

A novel facile solid‐phase organic synthesis of aryl vinyl ethers by reaction of polystyrene‐supported 2‐phenylsulfonylethanol with phenols under Mitsunobu conditions and subsequent elimination reaction with DBU has been developed. The advantages of this method include straightforward operation, good yield and high purity of the products. Alternatively, a typical example of Suzuki coupling reaction on‐resin was further applied to prepare 4‐phenylphenyl vinyl ether for extending this method.