287724-99-6

Upstream product

• 65-85-0 benzoic acid 
• 210548-19-9 (3R,4R,5S)-4-Benzyloxy-5-benzyloxymethyl-tetrahydro-thiophen-3-ol 

Downstream Products

• 287725-01-3 Benzoic acid (2S,3S,4R,5S)-4-benzyloxy-5-benzyloxymethyl-2-(6-chloro-purin-9-yl)-tetrahydro-thiophen-3-yl ester 
• 287725-03-5 (2S,3S,4R,5S)-4-Benzyloxy-5-benzyloxymethyl-2-(6-chloro-purin-9-yl)-tetrahydro-thiophen-3-ol 
• 287725-00-2 Benzoic acid (3S,4R,5S)-2-acetoxy-4-benzyloxy-5-benzyloxymethyl-tetrahydro-thiophen-3-yl ester 
• 287725-02-4 9-((2S,4R,5S)-4-Benzyloxy-5-benzyloxymethyl-tetrahydro-thiophen-2-yl)-6-chloro-9H-purine 

Relevant academic research and scientific papers

A highly efficient synthesis of L-β-2′-deoxy-4′-thio-1′-purine nucleosides as potential antiviral agents

L-β-2′-Deoxy-4′-thio-1′-purine nucleosides were synthesized efficiently utilizing the neighboring group effect of the 2-benzoyl-4-thiosugar acetate. The Royal Society of Chemistry 2000.

Participation of sulfur occurred during the Mitsunobu reaction: Synthesis of novel isodideoxythionucleosides

Novel isodideoxythionucleosides have been synthesized from our versatile intermediate, L-4-thioarabitol derivative 5 using the Mitsunobu reaction as a key step. It is found that the sulfur atom of the 4-thiofuranose derivative takes part in the Mitsunobu