Synthesis of C-nucleosides from non-carbohydrate precursors. A 2,4-dioxoimidazolidin-5-yl ribofuranoside
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference5 articles.
1. High pressure mediated Diels-Alder reaction of furan with dialkyl (acetoxymethylene)malonate
2. Highly stereoselective total synthesis of .beta.-ribofuranosylmalonate
3. High-pressure mediated Diels-Alder reaction of di-l-menthyl acetoxy-methylenemalonate with furan: Enantioselective synthesis of β-D-ribofuranosylmalonate, a prospective synthon for C-nucleoside
4. C -Nucleosides and Related Compounds. IV. The Synthesis and Chemistry of D,L-2,5-Anhydroallose Derivatives
5. Stereospecificity of the photorearrangement of nitronate anions and its utilization for stereospecific cleavage of cyclic compounds
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