Phosphine-catalyzed chemodivergent reactions of para-quinone methides (p-QMs) affording a wide variety of diarylmethyl thioether derivatives have been reported. In the transformation presented in this work, P(4-FC6H4)3 catalyzed the direct 1,6-add...
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Recent Advances of 2‐Nitroglycals as Powerful Glycosyl Donors
Von Wiley-VCH zur Verfügung gestellt
2-Nitroglycals are important synthons for biological active 2-aminoglycosides, glycoconjugates and natural products synthesis. Herein, we summarized the recent advance of 2-nitroglycals from 2014 to 2023. A plethora of applications on the synthesis of bioactive compounds via Michael–type addition, sugar ring opening reaction, Ferrier rearrangement were summarized. Organo–catalysis glycosylation plays a pivotal role in these applications.
Abstract
2-Nitroglycals are important synthons for biological active 2-aminoglycosides, glycoconjugates and natural products synthesis. Herein, we summarized the recent advances of 2-nitroglycals including its synthetic methods and its applications. Using 2-nitroglycals, 2-aminoglycosides, nitro-polyol derivatives, sugar-furan derivatives, sugar-pyrrole molecules, 2,3-diaminoglycosides and 2-amino-1,3-dithioglycosides were obtained via Michael–type addition, retro-Henry-type reaction, C1/C3-Ferrier rearrangement and [3+2] N-heterocyclic addition. Most of these conversions are achieved via mild organo-catalysis glycosylation methods.
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