scholarly journals Correction: DNA-catalyzed glycosylation using aryl glycoside donors

2016 ◽  
Vol 52 (68) ◽  
pp. 10439-10439
Author(s):  
Anthony R. Hesser ◽  
Benjamin M. Brandsen ◽  
Shannon M. Walsh ◽  
Puzhou Wang ◽  
Scott K. Silverman
Keyword(s):  
Aryl Glycoside

Correction for ‘DNA-catalyzed glycosylation using aryl glycoside donors’ by Anthony R. Hesser et al., Chem. Commun., 2016, 52, 9259–9262.

Four Orders of Magnitude Rate Increase in Artificial Enzyme-Catalyzed Aryl Glycoside Hydrolysis

2005 ◽  
Vol 70 (18) ◽  
pp. 7217-7226 ◽  
Author(s):  
Fernando Ortega-Caballero ◽  
Jeannette Bjerre ◽  
Line Skall Laustsen ◽  
Mikael Bols
Keyword(s):  
Rate Increase ◽  
Artificial Enzyme ◽  
Glycoside Hydrolysis ◽  
Aryl Glycoside

Expeditious Routes to Evernitrose and Vancosamine Derivatives and Synthesis of a Model Vancomycin Aryl Glycoside

1998 ◽  
Vol 37 (13-14) ◽  
pp. 1871-1874 ◽  
Author(s):  
K. C. Nicolaou ◽  
Helen J. Mitchell ◽  
Floris L. van Delft ◽  
Frank Rübsam ◽  
Rosa M. Rodríguez
Keyword(s):  
Aryl Glycoside

A Metal-free and β-Stereoselective Synthesis of 2-Deoxy-C-aryl Glycosides: Synthesis of 5-aza analogues of Aquayamycin

Synlett ◽  
2021 ◽  
Author(s):  
Yuling Mei ◽  
nan jiang ◽  
Yu Yang ◽  
Wan Zhang ◽  
Saifeng Qiu ◽  
...  
Keyword(s):  
Stereoselective Synthesis ◽  
Metal Free ◽  
Wide Range ◽  
One Step ◽  
Aryl Glycosides ◽  
Aryl Glycoside

A convenient protocol for β-stereoselective synthesis of 2-deoxy-C-aryl glycosides has been developed. This reaction takes place in one step by using I2/Et3SiH to activate glycosyl acetate to generate glycosyl iodide intermediate in situ, which was captured by naphthol followed by Fries-like O- → C-glycoside rearrangement to selectively afford β-C-aryl glycoside. The approach is applicable to a wide range of naphthol modules, and its utility was demonstrated in the synthesis of 5-aza analogues of Aquayamycin.

ChemInform Abstract: METABOLITES OF PROTEACEAE. PART 9. EXIMIN (6-O-BENZOYLARBUTIN) AND THE SYNTHESIS OF ARYL GLYCOSIDE ESTERS

1979 ◽  
Vol 10 (13) ◽  
Author(s):  
G. W. PEROLD ◽  
M. E. K. ROSENBERG ◽  
A. S. HOWARD ◽  
P. A. HUDDLE
Keyword(s):  
Aryl Glycoside

scholarly journals DNA-catalyzed glycosylation using aryl glycoside donors

2016 ◽  
Vol 52 (59) ◽  
pp. 9259-9262 ◽  
Author(s):  
Anthony R. Hesser ◽  
Benjamin M. Brandsen ◽  
Shannon M. Walsh ◽  
Puzhou Wang ◽  
Scott K. Silverman
Keyword(s):  
Aryl Glycosides ◽  
Aryl Glycoside ◽  
Glycosyl Donors

Using both β and α anomers of aryl glycosides as the glycosyl donors, we used in vitro selection to identify deoxyribozymes that glycosylate 3′-OH of a DNA oligonucleotide.

C-Aryl glycoside inhibitors of SGLT2: Exploration of sugar modifications including C-5 spirocyclization

2010 ◽  
Vol 20 (5) ◽  
pp. 1569-1572 ◽  
Author(s):  
Ralph P. Robinson ◽  
Vincent Mascitti ◽  
Carine M. Boustany-Kari ◽  
Christopher L. Carr ◽  
Patrick M. Foley ◽  
...  
Keyword(s):  
Aryl Glycoside

scholarly journals Unified strategy for the synthesis of C-aryl glycosides

2003 ◽  
Vol 75 (1) ◽  
pp. 63-70 ◽  
Author(s):  
S. F. Martin
Keyword(s):  
Unified Approach ◽  
Formal Synthesis ◽  
Palladium Catalyzed ◽  
Acid Catalyzed ◽  
Integrated Approaches ◽  
Aryl Glycosides ◽  
Aryl Glycoside

A unified approach for the synthesis of the four major groups of C-aryl glycosides has been developed. The strategy incorporates two integrated approaches, the first of which features the [4+2] cycloaddition of a glycosyl furan with a substituted benzyne followed by the acid-catalyzed opening of the resultant adduct. The second route involves the sequential palladium-catalyzed opening of a benzyne-furan cycloadduct with an iodo glycal followed by oxidation of the resultant dihydronaphthol ring and reduction of the glycal moiety. The utility of this strategy has been established by a concise formal synthesis of the C-aryl glycoside antibiotic galtamycinone.

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