Stereoselective Glycosylation of Glucosamine: The Role of theN-Protecting Group

2012 ◽  
Vol 7 (11) ◽  
pp. 2482-2501 ◽  
Author(s):  
Ramu Enugala ◽  
Luísa C. R. Carvalho ◽  
Marina J. Dias Pires ◽  
M. Manuel B. Marques
ChemInform ◽  
2013 ◽  
Vol 44 (15) ◽  
pp. no-no
Author(s):  
Ramu Enugala ◽  
Luisa C. R. Carvalho ◽  
Marina J. Dias Pires ◽  
M. Manuel B. Marques

2012 ◽  
Vol 8 ◽  
pp. 456-460 ◽  
Author(s):  
Toshiki Nokami ◽  
Akito Shibuya ◽  
Yoshihiro Saigusa ◽  
Shino Manabe ◽  
Yukishige Ito ◽  
...  

Glycosyl triflates with a 2,3-oxazolidinone protecting group were generated from thioglycosides by low-temperature electrochemical oxidation. The glycosyl triflates reacted with alcohols to give the corresponding glycosides β-selectively at low temperatures. However, α-selectivity was observed in the absence of base at elevated reaction temperatures. In situ generated triflic acid promotes the isomerization of β-products to α-products.


ChemInform ◽  
2015 ◽  
Vol 46 (27) ◽  
pp. no-no
Author(s):  
Maria Sanchez-Rosello ◽  
Javier Miro ◽  
Carlos del Pozo ◽  
Santos Fustero

2015 ◽  
Vol 171 ◽  
pp. 60-66 ◽  
Author(s):  
María Sánchez-Roselló ◽  
Javier Miró ◽  
Carlos del Pozo ◽  
Santos Fustero

2004 ◽  
Vol 29 (1-6) ◽  
pp. 115-121 ◽  
Author(s):  
Margit Preiml ◽  
Helmut Hönig ◽  
Norbert Klempier
Keyword(s):  

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