396131-30-9

Upstream product

• 3601-89-6 Hoffer's chlorosugar 
• 65032-27-1 ethynylmagnesium chloride 
• 4330-21-6 2-deoxy-3,5-di-O-p-toluoyl-α-D-erythro-pentofuranosyl chloride 
• 4301-14-8 acetylenemagnesium bromide 

Downstream Products

• 1207741-12-5 1-[(2-thienyl)ethynyl]-1,2-dideoxy-3,5-di-O-(4-toluoyl)-α-D-ribofuranose 
• 1207741-13-6 1-[(3-thienyl)ethynyl]-1,2-dideoxy-3,5-di-O-(4-toluoyl)-α-D-ribofuranose 
• 1207741-14-7 1-[(2-pyridyl)ethynyl]-1,2-dideoxy-3,5-di-O-(4-toluoyl)-α-D-ribofuranose 
• 1207741-15-8 1-[(3-pyridyl)ethynyl]-1,2-dideoxy-3,5-di-O-(4-toluoyl)-α-D-ribofuranose 
• 1207741-16-9 1-[(2,2'-bipyridin-5-yl)ethynyl]-1,2-dideoxy-3,5-di-O-(4-toluoyl)-α-D-ribofuranose 
• 1115184-32-1 1,4-bis[1,2-dideoxy-3,5-di-O-(4-toluoyl)-α-D-ribofuranosyl]butadiyne 
• 1207741-11-4 1-[(4-methoxyphenyl)ethynyl]-1,2-dideoxy-3,5-di-O-(4-toluoyl)-α-D-ribofuranose 
• 1207741-17-0 1-[(1-pyrenyl)ethynyl]-1,2-dideoxy-3,5-di-O-(4-toluoyl)-α-D-ribofuranose 
• 1207741-10-3 1-[(4-cyanophenyl)ethynyl]-1,2-dideoxy-3,5-di-O-(4-toluoyl)-α-D-ribofuranose 
• 1207741-09-0 1-[(4-methoxycarbonylphenyl)ethynyl]-1,2-dideoxy-3,5-di-O-(4-toluoyl)-α-D-ribofuranose 
• 1332828-73-5 bis-(O-toluoyl)-1α-{[2-(N-trifluoroacyl)-5-chlorophenyl]ethynyl}deoxyribose 
• 1332828-71-3 bis-(O-toluoyl)-1α-{[2-(N-trifluoroacyl)phenyl]ethynyl}deoxyribose 
• 1332828-79-1 bis-(O-toluoyl)-1α-(1H-indol-2-yl)deoxyribose 
• 1332828-72-4 bis-(O-toluoyl)-1α-{[2-(N-trifluoroacyl)-4-chlorophenyl]ethynyl}deoxyribose 

Relevant academic research and scientific papers

Sonogashira reactions of α- and β-1-ethynyl-2-deoxyribosides: synthesis of acetylene-extended C-nucleosides

An improved practical protocol for the synthesis of both anomers of 1-ethynyl-2-deoxiribosides 1 was developed. The Sonogashira coupling of ethynyldeoxyribosides 1 with various aryl- and heteroaryl halides was carried out under various conditions. It was

Synthesis of C-aryldeoxyribosides by [2 + 2 + 2]-cyclotrimerization catalyzed by Rh, Ni, Co, and Ru complexes

A novel approach to the synthesis of functionalized C-nucleosides was developed. Cyclotrimerization of C-alkynyldeoxyriboside with a variety of substituted 1,6-heptadiynes to the corresponding C-aryldeoxyribosides was catalyzed by various transition metal