Deoxy-nitrosugars. 6th communication. Stereoelectronic control in the reductive denitration of tertiary nitro ethers. A synthesis of ?C-glycosides?-Reference-Cited by-同舟云学术

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Deoxy-nitrosugars. 6th communication. Stereoelectronic control in the reductive denitration of tertiary nitro ethers. A synthesis of ?C-glycosides?

Published:1983-11-02 Issue:7 Volume:66 Page:2210-2222
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:de
Short-container-title:Helv. Chim. Acta

Author:

Baumberger Franz,Vasella Andrea

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference63 articles.

1. Deoxy-nitrosugars. 5th Communication. The anomeric effect of the nitro group

2. Substitution reactions which proceed via radical anion intermediates. 20. Replacement of the nitro group by hydrogen

3. 1-Benzyl-1,4-dihydronicotinamide as a reagent for replacing aliphatic nitro groups by hydrogen: an electron-transfer chain reaction

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1. The Last Fortress of Tin's Tyranny – Protodenitration of Nitroalkanes;European Journal of Organic Chemistry;2023-01-31

2. Synthesis of C- and S-Glycosides;Comprehensive Glycoscience;2021

3. Lyxose and Ribose C -Glycosides;C-Furanosides;2018

4. galacto-C- Furanosides (I, β- C -Lyxose);C-Furanosides;2018

5. Construction of quaternary stereocentres on carbohydrate scaffolds;RSC Advances;2016

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