374694-90-3

Upstream product

• 21740-23-8 3,5-O-bis(4-chlorobenzoyl)-2-deoxy-α-D-ribofuranosyl chloride 
• 491-30-5 1-isoquinolone 
• 374694-86-7 1-[3,5-bis-O-(p-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]isocarbostyril 

Downstream Products

• 374695-04-2 1-[3,5-bis-O-(p-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]-7-propynylisocarbostyril 
• 374695-00-8 1-[3,5-bis-O-(p-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]-7-iodoethynylisocarbostyril 
• 374695-01-9 1-[3,5-bis-O-(p-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]-7-(2-bromoethynyl)isocarbostyril 
• 374694-98-1 1-[3,5-bis-O-(p-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]-7-(2-trimethylsilylethynyl)isocarbostyril 
• 374694-94-7 1-[3,5-bis-O-(p-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]-7-cyanoisocarbostyril 
• 374694-92-5 1-[3,5-bis-O-(p-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]-7-trifluoromethylisocarbostyril 

Relevant academic research and scientific papers

Synthesis of unnatural 7-substituted-1-(2-deoxy-β-D-ribofuranosyl)isocarbostyrils: "Thymine replacement" analogs of deoxythymidine for evaluation as antiviral and anticancer agents

A group of unnatural 1-(2-deoxy-β-D-ribofuranosyl)isocarbostyrils having a variety of C-7 substituents [H, 4,7-(NO2)2, I, CF3, CN, (E)-CH=CH-I, -C≡CH, -C≡C-I, -C≡C-Br, -C≡C-Me], designed as nucleoside mimics, were synthesi