scholarly journals Chondroitinase-mediated Degradation of Rare 3-O-Sulfated Glucuronic Acid in Functional Oversulfated Chondroitin Sulfate K and E

2007 ◽  
Vol 282 (51) ◽  
pp. 36895-36904 ◽  
Author(s):  
Duriya Fongmoon ◽  
Ajaya Kumar Shetty ◽  
Basappa ◽  
Shuhei Yamada ◽  
Makiko Sugiura ◽  
...  
1996 ◽  
Vol 271 (43) ◽  
pp. 26745-26754 ◽  
Author(s):  
Kazuyuki Sugahara ◽  
Yukako Tanaka ◽  
Shuhei Yamada ◽  
Nobuko Seno ◽  
Hiroshi Kitagawa ◽  
...  

1988 ◽  
Vol 540 (1 Advances in N) ◽  
pp. 442-444
Author(s):  
SCOTT McGINNIS ◽  
TATSUO KOHRIYAMA ◽  
ROBERT K. YU ◽  
MICHAEL A. PESCE ◽  
NORMAN LATOV

2008 ◽  
Vol 217 (3) ◽  
pp. 769-777 ◽  
Author(s):  
Tatsuya Miyazaki ◽  
Satoshi Miyauchi ◽  
Akira Tawada ◽  
Takahisa Anada ◽  
Satoshi Matsuzaka ◽  
...  

Biochemistry ◽  
1973 ◽  
Vol 12 (20) ◽  
pp. 3898-3903 ◽  
Author(s):  
Martha E. Richmond ◽  
Silvana DeLuca ◽  
Jeremiah E. Silbert

2019 ◽  
Vol 15 ◽  
pp. 137-144 ◽  
Author(s):  
Teresa Mena-Barragán ◽  
José L de Paz ◽  
Pedro M Nieto

Here, we present an exploratory study on the fluorous-assisted synthesis of chondroitin sulfate (CS) oligosaccharides. Following this approach, a CS tetrasaccharide was prepared. However, in contrast to our previous results, a significant loss of β-selectivity was observed in [2 + 2] glycosylations involving N-trifluoroacetyl-protected D-galactosamine donors and D-glucuronic acid (GlcA) acceptors. These results, together with those obtained from experiments employing model monosaccharide building blocks, highlight the impact of the glycosyl acceptor structure on the stereoselectivity of glycosylation reactions. Our study provides useful data about the substitution pattern of GlcA units for the efficient synthesis of CS oligomers.


Sign in / Sign up

Export Citation Format

Share Document