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Journal ArticleDOI

The preparation of C-arylglycals. The palladium-catalyzed coupling of 3,4,6-tri-O-(tert-butyldimethylsilyl)-1-(tributylstannyl)-D-glucal and aryl bromides

Richard Friesen, +1 more
- 01 Apr 1990 - 
- Vol. 55, Iss: 9, pp 2572-2574
TLDR
The palladium-catalyzed couplings of the protected 1-(tributylstannyl)-D-glucal 1 and substituted aryl bromides provide the corresponding C-arylglucals and a dimer as mentioned in this paper.
Abstract
The palladium-catalyzed couplings of the protected 1-(tributylstannyl)-D-glucal 1 and substituted aryl bromides provide the corresponding C-arylglucals and a dimer

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Journal ArticleDOI

1,4-Dihydropyridines as Alkyl Radical Precursors: Introducing the Aldehyde Feedstock to Nickel/Photoredox Dual Catalysis

TL;DR: A Ni/photoredox dual catalytic cross-coupling is disclosed in which a diverse range of (hetero)aryl bromides are used as electrophiles, with 1,4-dihydropyridines serving as precursors to Csp3-centered alkyl radical coupling partners.
Journal ArticleDOI

Total Synthesis of Aryl C-Glycoside Natural Products: Strategies and Tactics

TL;DR: The aryl C-glycoside structure is, among the plenty of biologically active natural products, one of the distinct motifs embedded, and the synthetic strategies and tactics employed in the total synthesis of this class of natural products.
Book ChapterDOI

Nucleophilic C-glycosyl donors for C-glycoside synthesis

TL;DR: A review of the methods available for the synthesis of C-glycosides that involve the use of carbohydrate units expressing nucleophilic reactivity at C(1) (the anomeric site) is given in this article.
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