Stereoselective Synthesis of Glycosides <i>via</i> Tsuji-Trost Type Glycosylation Using 3,4-Carbonate Galactals
  • Kim, Ye Lim
  • Kim, Ju Hyun
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초록

Pd-catalyzed stereoselective glycosylations using unsaturated sugar derivatives, glycals, have been successfully achieved in recent years. This review focuses on approaches to control the stereoselectivities of glycosides via pi-allyl intermediates that mimic the Tsuji-Trost asymmetric allylic alkylation reactions, enabling stereoselectivity control through rational design. In the reaction process, zwitterionic Pd-pi-allyl complexes, formed after the oxidative addition and decarboxylation, play a crucial role in increasing reactivities and enhancing the stereoselectivities of alpha- and beta-glycosides. We summarized recently developed Tsuji-Trost type glycosylations using 3,4-carbonate galactals, featuring high efficiency, exclusive stereoselectivities, and a broad reaction scope including O-, N-, S-, and C-glycosylations.

키워드

Tsuji-Trost AAAPd-pi-allyl complexesstereoselective glycosylationsglycalsglycosidesBETA-C-GLYCOSYLATIONO-GLYCOSYLATIONBOND FORMATIONBIOLOGICAL ROLESGLYCALSOLIGOSACCHARIDESFACILEACCESSAIR
제목
Stereoselective Synthesis of Glycosides <i>via</i> Tsuji-Trost Type Glycosylation Using 3,4-Carbonate Galactals
저자
Kim, Ye LimKim, Ju Hyun
DOI
10.1002/tcr.202400067
발행일
2024-09
유형
Review
저널명
Chemical Record
24
9