%0 Journal Article
%A Cheng, Xuhong
%A Khan, Noshena
%A Kumaran, Govindaraj
%A Mootoo, David R.
%D 2001
%T A Convergent Strategy for the Synthesis
of β-Carba-galacto-disaccharides
%U https://acs.figshare.com/articles/journal_contribution/A_Convergent_Strategy_for_the_Synthesis_of_-Carba-galacto-disaccharides/3738861
%R 10.1021/ol0156906.s001
%2 https://ndownloader.figshare.com/files/5830629
%K Convergent Strategy
%K ether
%K glycone
%K carbasugar ring
%K monosaccharide alcohols
%K cyclization
%K synthesis
%K 23 b
%K component
%K ion
%K formation
%K convergent strategy
%K aglycone
%K preparation
%K Synthesi
%K oxocarbenium
%X A convergent strategy for the synthesis of β-carba-galacto-disaccharides is illustrated by the preparation of 1 and 4, from a central “glycone”
component 22, and the corresponding “aglycone” segments, monosaccharide alcohols, 23a or 23b. The key step is the formation of the
carbasugar ring via an oxocarbenium ion−enol ether cyclization
%I ACS Publications