Abstract
1,3-Oxazolidine-2-thiones fused to ketohexose backbone were prepared from 1-O-, 1-N- or 1-Sderivatives in reasonable yields. Spontaneous ring closure leads to spiro-tricyclic unexpected aminal and amide structures.
Keywords: 1,3-oxazolidine-2-thione, ketohexoses, l-sorbose, d-fructose
Related Books
2-Deoxy-D-Glucose: Chemistry and Biology
Chiral Ionic Liquids: Applications in Chemistry and Technology
Basics of Organic Chemistry: A Textbook for Undergraduate Students
Advances in Organic Synthesis
The Synthetic Methods, Structures, and Properties of the Ca-C σ Bond Organocalcium Containing Compounds
Advances in Organic Synthesis
Chemistry of Bipyrazoles: Synthesis and Applications
Advances in Organic Synthesis
Advanced Nanocatalysis for Organic Synthesis and Electroanalysis
Advances in Organic Synthesis
20