4.1 Article

Transition-metal-catalyzed C-N cross-coupling reactions of N-unsubstituted sulfoximines: a review

期刊

JOURNAL OF SULFUR CHEMISTRY
卷 39, 期 6, 页码 674-698

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/17415993.2018.1471142

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Sulfoximines; cross-coupling reactions; N-alkylation; N-alkenylation; N-alkynylation; N-arylation; palladium; copper

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In recent years, N-functionalized sulfoximines have attracted the significant attention of medicinal chemists due to their wide spectrum of biological activities. This class of organosulfur compounds has also found a number of applications in agricultural chemistry. In addition to these benefits, sulfoximines are one of the most important and versatile chiral auxiliaries and ligands in asymmetric syntheses. As a result of these, numerous efforts have been devoted to the development of effective strategies towards the synthesis of N-functionalized sulfoximines. An efficient, practical, and versatile strategy for the synthesis of titled compounds involves the transition-metal-catalyzed cross-coupling reactions of easily accessible NH-sulfoximines with various electrophilic partners. In this review, we highlight a number of recent discoveries and advances in this interesting and important research arena. The N-alkylation reactions are discussed first. This is followed by metal-catalyzed N-alkenylation and N-alkynylation reactions. Finally, N-arylation reactions will be covered at the end of the review. [GRAPHICS] .

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