ChemInform Abstract: Glycosylation via Remote Activation of Anomeric Leaving Groups: Development of 2-(2-Propylsulfinyl)benzyl Glycosides as Novel Glycosyl Donors.

ChemInform ◽  
2016 ◽  
Vol 47 (24) ◽  
Author(s):  
Qian Wan ◽  
et al.
Keyword(s):  
Leaving Groups ◽  
Glycosyl Donors

ChemInform Abstract: Glycosyl Donors with Phosphorimidate Leaving Groups for Either α- or β-Glycosidation.

ChemInform ◽  
2010 ◽  
Vol 28 (47) ◽  
pp. no-no
Author(s):  
S. PAN ◽  
H. LI ◽  
F. HONG ◽  
B. YU ◽  
K. ZHAO
Keyword(s):  
Leaving Groups ◽  
Glycosyl Donors

Glycosylation via remote activation of anomeric leaving groups: development of 2-(2-propylsulfinyl)benzyl glycosides as novel glycosyl donors

2016 ◽  
Vol 3 (2) ◽  
pp. 177-183 ◽  
Author(s):  
Penghua Shu ◽  
Wang Yao ◽  
Xiong Xiao ◽  
Jiuchang Sun ◽  
Xiang Zhao ◽  
...  
Keyword(s):  
Leaving Groups ◽  
Glycosyl Donors

New glycosyl donors with recyclable and regenerable leaving groups, which could be activated via remote mode, were designed for latent-active glycosylation.

GLYCOSYL DONORS WITH PHOSPHORIMIDATE LEAVING GROUPS FOR EITHER α- OR β- GLYCOSIDATION

1997 ◽  
Vol 38 (35) ◽  
pp. 6139-6142 ◽  
Author(s):  
Shifeng Pan ◽  
Hao Li ◽  
Feng Hong ◽  
Biao Yu ◽  
Kang Zhao
Keyword(s):  
Leaving Groups ◽  
Glycosyl Donors

Oligosaccharide synthesis based on glycosyl donors and acceptors carrying phosphorus-containing leaving groups

1997 ◽  
Vol 38 (29) ◽  
pp. 5181-5184 ◽  
Author(s):  
Shun-ichi Hashimoto ◽  
Hiroki Sakamoto ◽  
Takeshi Honda ◽  
Shiro Ikegami
Keyword(s):  
Oligosaccharide Synthesis ◽  
Phosphorus Containing ◽  
Leaving Groups ◽  
Glycosyl Donors

The effect of steric size of leaving group on rates of the competing syn- and anti-pathways in biomolecular elimination

1980 ◽  
Vol 45 (8) ◽  
pp. 2171-2178
Author(s):  
Jiří Závada ◽  
Magdalena Pánková
Keyword(s):  
Comparative Analysis ◽  
Homologous Series ◽  
Leaving Group ◽  
Leaving Groups

Approximate rates of the competing syn- and anti-pathways have been determined in t-C4H9OK-t-C4H9OH promoted elimination from two homologous series of tosylates: I-OTs trans-III (R = H, CH3, C2H5, n-C3H7, i-C3H7, t-C4H9) and II-OTs trans-IV (R = CH3, C2H5, n-C3H7, i-C3H7, t-C4H9). A comparison has been made with rates of the same processes in the (+) elimination of the corresponding trimethylammonium salts I-N(CH3)3 trans-III and (+) II-N(CH3)3 trans-IV. The title effect is demonstrated by a comparative analysis of the rate patterns obtained for the two leaving groups.

Sign in / Sign up

Export Citation Format

Share Document