81366-70-3

Usage

Uses

Used in Biochemical Research:
2-Deoxy-N-phenyl-D-erytho-pentofuranosylamine is used as a subject of study in biochemical research for its distinctive structure and potential interactions with biological systems, which may lead to the discovery of new applications or insights into biological processes.
Used in Pharmaceutical Development:
Although its biological activity and toxicity are not well-documented, 2-Deoxy-N-phenyl-D-erytho-pentofuranosylamine is used as a candidate for pharmaceutical research, with the potential to be developed into new drugs or therapeutic agents once its properties are better understood.
Used in Chemical Synthesis:
As a monosaccharide with a unique structure, 2-Deoxy-N-phenyl-D-erytho-pentofuranosylamine is used in chemical synthesis for creating novel compounds or modifying existing ones, potentially leading to advancements in various chemical industries.
Note: The specific applications listed above are speculative based on the general properties of monosaccharides and the need for further research. The actual uses of 2-Deoxy-N-phenyl-D-erytho-pentofuranosylamine may vary once its properties and potential are fully explored.

Upstream product

• 104578-83-8 methyl (3S,4R)-3-(tert-butyldimethylsiloxy)-4,5-(isopropylidenedioxy)pentanoate 
• 34371-14-7 2-deoxy-D-ribono1,4-lactone 
• 62-53-3 aniline 
• 34371-14-7 2-deoxy-D-ribonolactone 
• 81366-66-7 3-Acetoxy-3-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-propionic acid ethyl ester 
• 274908-67-7 Ethyl (4''R)-(2,2-dimethyl-1,3-dioxolan-4-yl)-3-hydroxypropionate 
• 81366-68-9 (4S,5R)-4-acetoxy-5-(hydroxymethyl)-4,5-dihydrofuran-2(3H)-one 
• 452-51-7 D-2-deoxyribose 

Relevant academic research and scientific papers

Ni-catalyzed homoallylation of polyhydroxy N,O- Acetals with conjugated dienes promoted by triethylborane

In the presence of Ni-catalyst and triethylborane, N,O- Acetals prepared from glycolaldehyde and glyceraldehyde with primary amines in situ underwent homoallylation with conjugated dienes to provide 2- Amino-5-hexenols in high regio- And stereoselectivity

Chemistry of O-Silylated Ketene Acetals: Stereocontrolled Synthesis of 2-Deoxy- and 2-Deoxy-2-C-alkyl-erythro-pentoses

Diastereoselective aldol reactions of 2,3-O-isopropylidene-D-(and L-)-glyceraldehydes (D- and L-2) with ketene silyl acetal 1a occurred in acetonitrile under mild conditions to give the corresponding anti-β-siloxy esters (D- and L-3a) as major products, which were converted to 2-deoxy-D-(and L-) riboses through a few additional steps.The aldol reactions of D-2 with α-monoalkyl-substituted ketene silyl acetals 1c-f proceeded similarly to give all anti-α-alkyl-β-siloxy esters (11a-14a) as major products, which were converted into 2-deoxy-2-C-alkyl-erythro-pentoses (17a,b).

THE CHEMISTRY OF O-SILYLATED KETENE ACETALS; DIASTEREOSELECTIVE ALDOL REACTION OF 2,3-O-ISOPROPYLIDENE-D (AND L)-GLYCERALDEHYDES LEADING TO 2-DEOXY-D (AND L)-RIBOSES

Diastereoselective carbon-carbon bond forming reaction of 2,3-O-isopropylidene-D (and L)-glyceraldehydes (D and L-2) with ketene silyl acetals (1a,b) occured in acetonitrile under mild conditions to give the corresponding anti-β-siloxyesters (D and L-3a) as major products, which could be converted through a few additional steps to 2-deoxy-D (and L)-riboses.

A NEW METHOD FOR THE GENERATION OF A BORON ENOLATE OF AN ESTER - A NEW SYNTHESIS OF 2-DEOXY-D-RIBOSE -

A boron enolate of an ester was generated in situ by the treatment of ethoxyacetylene with mercury(II) acetate and diphenylborinic acid, and the boron enolate thus formed further reacted with aldehydes to give β-hydroxyesters and β-acetoxyesters in good yields.The reaction was successfully applied to the stereoselective synthesis of 2-deoxy-D-ribose.