New method for regioselective glycosylation employing saccharide oxyanions
M Matwiejuk, J Thiem
Index: Matwiejuk, Martin; Thiem, Joachim European Journal of Organic Chemistry, 2011 , # 29 p. 5860 - 5878
Full Text: HTML
Citation Number: 6
Abstract
Abstract As an alternative concept for glycosylation, the prior activation of acceptor hydroxy groups for selective glycosidic bond formation, was investigated to give complex oligosaccharides. Oxyanions obtained from partially protected saccharides were glycosylated by employing glycopyranosyl halides, and the regiochemical results were studied. Initially, partially methylated methyl-α-D-glucopyranosides were used as a model ...
Related Articles:
[Nishi, Yuki; Tanimoto, Toshiko Bioscience, Biotechnology and Biochemistry, 2009 , vol. 73, # 3 p. 562 - 569]
[Kondo, Hirosato; Aoki, Shin; Ichikawa, Yoshitaka; Halcomb, Randall L.; Ritzen, Helena; Wong, Chi-Huey Journal of Organic Chemistry, 1994 , vol. 59, # 4 p. 864 - 877]
[Misra, Anup Kumar; Agnihotri, Geetanjali Carbohydrate Research, 2004 , vol. 339, # 4 p. 885 - 890]
[Kondo, Hirosato; Aoki, Shin; Ichikawa, Yoshitaka; Halcomb, Randall L.; Ritzen, Helena; Wong, Chi-Huey Journal of Organic Chemistry, 1994 , vol. 59, # 4 p. 864 - 877]
[Kondo, Hirosato; Aoki, Shin; Ichikawa, Yoshitaka; Halcomb, Randall L.; Ritzen, Helena; Wong, Chi-Huey Journal of Organic Chemistry, 1994 , vol. 59, # 4 p. 864 - 877]