Application of dialkyl azodicarboxylate frameworks featuring multi-functional properties. Issue 11 (23rd April 2019)

• Record Type: Journal Article
• Authors: Usman, Muhammad; Zhang, Xiao-Wen; Wu, Di; Guan, Zheng-Hui; Liu, Wen-Bo
• Is Part Of: Organic chemistry frontiers. Volume 6:Issue 11(2019)
• Page Start: 1905
• Page End: 1928
• Publication Date: 2019-04-23
• Subjects: Chemistry, Organic -- Periodicals; 547.005
• DOI: 10.1039/c9qo00017h
• Languages: English
• ISSNs: 2052-4110

Abstract

Abstract : The application of dialkyl azodicarboxylates as versatile reagents in Mitsunobu, oxidation, electrophilic, amination and carbonylation reactions is reviewed. Abstract : Azo-disubstituted derivatives with electron-withdrawing groups, such as acyl, alkoxycarbonyl and nitrile, are widely used as reagents in organic synthesis. Dialkyl azodicarboxylates are the most readily available reagents among them. This review summarizes the utility of dialkyl azodicarboxylates as versatile reagents and essential building blocks for the synthesis of complex molecules. Applications of dialkyl azodicarboxylates in the Mitsunobu reaction, as oxidants in the oxidation of aldehydes, hydrazines, alcohols, hydroxylamines and thiols, and in photocatalytic C–C bond cleavage and C–H bond amination reactions are discussed. In synthetic chemistry, a large number of synthetic procedures use azodicarboxylates as electrophiles. The discussion is also extended toward the enantioselective α-amination of carbonyl, cyanoacetate and heterocycle derivatives. In addition, mechanistic insights are also briefly reviewed.