Abstract
The present account reports on the E-α,β-unsaturated-δ-butoxycarbonyl-δ-hydroxy-aldehyde (3), acetal hydroperoxide (4) and α,β-unsaturated-δ-lactone (5), obtained during Zamojskis total synthesis of carbohydrates. Properties of these and related compounds, and their further applications in organic synthesis are discussed.
Keywords: Zamojski's Total Synthesis, Racemic Monosaccharides, Stereoselective Transformations, Sugar Synthons, carbohydrates, organic synthesis, Anomeric Hydroperoxides
Current Organic Chemistry
Title: Zamojskis Total Synthesis of Racemic Monosaccharides as an Inspiration for Stereoselective Transformations of Readily Available Sugar Synthons
Volume: 12 Issue: 12
Author(s): Marek Chmielewski, Sebastian Stecko and Wioletta Kosnik
Affiliation:
Keywords: Zamojski's Total Synthesis, Racemic Monosaccharides, Stereoselective Transformations, Sugar Synthons, carbohydrates, organic synthesis, Anomeric Hydroperoxides
Abstract: The present account reports on the E-α,β-unsaturated-δ-butoxycarbonyl-δ-hydroxy-aldehyde (3), acetal hydroperoxide (4) and α,β-unsaturated-δ-lactone (5), obtained during Zamojskis total synthesis of carbohydrates. Properties of these and related compounds, and their further applications in organic synthesis are discussed.
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Cite this article as:
Chmielewski Marek, Stecko Sebastian and Kosnik Wioletta, Zamojskis Total Synthesis of Racemic Monosaccharides as an Inspiration for Stereoselective Transformations of Readily Available Sugar Synthons, Current Organic Chemistry 2008; 12 (12) . https://dx.doi.org/10.2174/138527208785161150
DOI https://dx.doi.org/10.2174/138527208785161150 |
Print ISSN 1385-2728 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5348 |
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