Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Stereoselective P-Mannosylation on Polymer Support

The Institute of Physical and Chemical Research (RIKEN), Wako-shi, Saitama, Japan [Pg.135]

A drastically distinct use of a polymer support in oligosaccharide synthesis was devised in connection with p-methoxybenzyl (PMB)-assisted intramolecular [Pg.138]

1 p-METHOXYBENZYL-ASSISTED INTRAMOLECULAR AGLYCON DELIVERY HIGHLY EFFICIENT P-MANNOSYLATION [Pg.139]

Seeking for general and highly stereoselective P-mannosylation, our attention was drawn to the approach based on the emerging concept of intramolecular aglycon [Pg.146]

Since all hydroxyl groups of the p-linked mannose residue can be distinguished, stereo- and regiocontrolled synthetic routes to essentially all types of Asn-linked glycans can be conceived. This aspect was demonstrated by the synthesis of [Pg.154]


See other pages where Stereoselective P-Mannosylation on Polymer Support is mentioned: [Pg.135]    [Pg.136]    [Pg.138]    [Pg.140]    [Pg.142]    [Pg.146]    [Pg.148]    [Pg.152]    [Pg.154]    [Pg.156]    [Pg.158]    [Pg.160]    [Pg.135]    [Pg.136]    [Pg.138]    [Pg.140]    [Pg.142]    [Pg.146]    [Pg.148]    [Pg.152]    [Pg.154]    [Pg.156]    [Pg.158]    [Pg.160]    [Pg.161]   


SEARCH



Mannosyl

P-Stereoselectivity

© 2024 chempedia.info