Open AccessBenzylidene Acetal Fragmentation Route to 6‐Deoxy Sugars: Direct Reductive Cleavage in the Presence of Ether Protecting Groups, Permitting the Efficient, Highly Stereocontrolled Synthesis of β‐D‐Rhamnosides from D‐Mannosyl Glycosyl Donors. Total Synthesis of α‐D‐Gal‐(1→3)‐α‐D‐Rha‐(1→3)‐β‐D‐Rha‐ (1→4)‐β‐D‐Glu‐OMe, the Repeating Unit of the Antigenic Lipopolysaccharide from Escherichia hermannii ATCC 33650 and 33652.
Author(s) -
Crich David,
Yao Qingjia
Publication year - 2004
Publication title -
cheminform
Language(s) - English
Resource type - Journals
eISSN - 1522-2667
pISSN - 0931-7597
DOI - 10.1002/chin.200444222
Subject(s) - chemistry , acetal , glycosyl , fragmentation (computing) , stereochemistry , glycosyl donor , ether , cleavage (geology) , combinatorial chemistry , organic chemistry , computer science , operating system , geotechnical engineering , engineering , fracture (geology)
For Abstract see ChemInform Abstract in Full Text.
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