Amanote Research
Register
Sign In
Selective Protection of 2-Azido-Lactose and in Situ Ferrier Rearrangement During Glycosylation: Synthesis of a Dimeric Lewis X Fragment
doi 10.1021/jo062541y.s002
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Synthesis of 2,3-Unsaturated O-Glycosides From Optically Active Alcohols via Ferrier Rearrangement: Configurational Studies
Journal of the Chilean Chemical Society
Chemistry
Efficient Carbon-Ferrier Rearrangement on Glycals Mediated by Ceric Ammonium Nitrate: Application to the Synthesis of 2-Deoxy-2-Amino-C-Glycoside
Beilstein Journal of Organic Chemistry
Organic Chemistry
Synthesis of Glycosyl Phosphates From 1, 2-Ortho Esters and Application to in Situ Glycosylation Reactions
Synthesis of a Sialic Acid A(2-3) Galactose Building Block and Its Use in a Linear Synthesis of Sialyl Lewis X
Total Synthesis of the Marine Natural Product (-)-Clavosolide A. A Showcase for the Petasis-Ferrier Union/Rearrangement Tactic
Cyanuric Chloride as an Efficient Catalyst for the Synthesis of 2,3-UnsaturatedO-Glycosides by Ferrier Rearrangement
The Scientific World Journal
Biochemistry
Medicine
Genetics
Molecular Biology
Environmental Science
Organic Azides. 5. A Simple Synthesis of Alkyl 3-Azido-2-Alkenoates.
Acta Chemica Scandinavica
Fragment-Based Discovery of Potent and Selective DDR1/2 Inhibitors
ACS Medicinal Chemistry Letters
Organic Chemistry
Biochemistry
Drug Discovery
Fragment-Based Discovery of Potent and Selective DDR1/2 Inhibitors
