Journal ArticleDOI
Synthesis of carbohydrate epoxides under phase-transfer conditions
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This article is published in Carbohydrate Research.The article was published on 1986-12-15. It has received 12 citations till now. The article focuses on the topics: Aldose & Acetal.read more
Citations
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Journal ArticleDOI
Modular Synthesis of Constrained Ethyl (cEt) Purine and Pyrimidine Nucleosides
TL;DR: The retrosynthetic approach to this complex class of drug precursors offers clear benefits over existing routes based on step count and efficiency.
Journal ArticleDOI
Efficient routes to pyranosidic homologated conjugated enals and dienes from monosaccharides
J. Cristobal Lopez,Eric Lameignere,C. Burnouf,María de los Angeles Laborde,Alberto A. Ghini,Alain Olesker,Gabor Lukacs +6 more
TL;DR: In this paper, three new processes for the obtention of pyranosidic dienes type B, and D and homologated conjugated enals A, have been designed in the context of the preparation of useful chiral building blocks from monosaccharides.
Journal ArticleDOI
Synthesis of glycosyl xanthates from reducing sugar derivatives under phase-transfer conditions
Wiesław Szeja,Jadwiga Bogusiak +1 more
Journal ArticleDOI
Stereocontrolled Synthesis of a Cn–Cn+7 Building Block (“Eastern Moiety”) for the Unnatural Enantiomers of Important Polyol,Polyene Antibiotics Based on a Ring‐Closing Metathesis and an Aldol Addition of a Lactone Enolate
TL;DR: In this paper, a stereocontrolled synthesis of epoxide 6, which represents the Cn-Cn+7 or “eastern moiety” building block for the title compounds, has been realized in 19 steps.
References
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Book ChapterDOI
Oxirane Derivatives of Aldoses
TL;DR: In this paper, the authors discuss methods available for their synthesis, with special reference to their ease of formation, together with their reactions and the methods available to their characterization, as well as their nomenclature system based on the anhydride principle.
Journal ArticleDOI
l-Idose aus d-Glucose, sowie ein neuer Weg zur l-Idomethylose
A. S. Meyer,T. Reichstein +1 more
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