442906-75-4

Upstream product

• 442906-74-3 C₂₆H₃₁N₅O₅ 
• 442906-73-2 (1S,2R,3R,4R)-1,6:7,8-bis-O-isopropylidene-4-(6-aminopurin-9-yl)-1,2,3-tris(hydroxymethyl)cyclopentanol 
• 442906-69-6 (1S,3S,4S,5R)-1,6:7,8-bis-O-isopropylidene-3-(4'-nitrobenzoyl)-1,4,5-tris(hydroxymethyl)cyclopentane-1,3-diol 
• 442906-72-1 C₁₉H₂₅ClN₄O₄ 
• 442906-60-7 (1S,3R,4S,5R)-1,6:7,8-bis-O-isopropylidene-1,4,5-tris(hydroxymethyl)cyclopentane-1,3-diol 
• 442906-70-9 (1S,3S,4S,5R)-1,6:7,8-bis-O-isopropylidene-1,4,5-tris(hydroxymethyl)cyclopentane-1,3-diol 
• 202402-54-8 (5S,7R,8S,9R)-8,9-Bis-hydroxymethyl-2,2-dimethyl-1,3-dioxa-spiro[4.4]nonan-7-ol 
• 87-42-3 6-chloropurine 
• 98-88-4 benzoyl chloride 
• 108-24-7 acetic anhydride 

Relevant academic research and scientific papers

Synthesis of novel hydroxymethyl substituted analogues related to carbovir and neplanocin A

Two enantiomerically pure hydroxymethyl substituted cyclopentene nucleoside analogues (42 and 53) related to carbovir and neplanocin A, respectively, were prepared from the chiral pool of iridoid glucosides. In addition two saturated hydroxymethylated ana