902455-29-2

Upstream product

• 474329-16-3 (-)-(1S)-1-[(4S,5S)-5-(hydroxymethyl)-2,2-dimethyl-5-vinyl[1,3]dioxolan-4-yl]prop-2-en-1-ol 
• 902455-27-0 (+)-(1S,2S,3R)-2,3-O-isopropylidene-3-(2-triphenylmetoxyethyl)-4-cyclopentenol 
• 902455-26-9 (+)-(1S,2S,3R)-2,3-O-isopropylidene-3-(2-hydroxyethyl)-4-cyclopentenol 
• 1067904-33-9 (3aR,6S,6aS)-6-Hydroxy-2,2-dimethyl-6,6a-dihydro-cyclopenta[1,3]dioxole-3a-carbaldehyde 
• 902455-25-8 (-)-(1S,2S,3R)-2,3-O-isopropylidene-3-vinyl-4-cyclopentenol 
• 902455-28-1 (+)-(1S,2S,3R)-2,3-O-isopropylidene-3-(2-triphenylmetoxyethyl)-4-cyclopentenyl p-toluenesulfonate 
• 66224-66-6 adenine 

Relevant academic research and scientific papers

Asymmetric synthesis of homo-apioneplanocin A from d-ribose

Homo-apioneplanocin A was efficiently synthesized via stereoselective hydroxymethylation, regio- and chemoselective hydroboration, and chemoselective oxidation as key steps from d-ribose.

Stereoselective synthesis of homo-apioneplanocin A as potential inhibitor of S-adenosylhomocysteine hydrolase

Homo-apioneplanocin A (1) as a potential inhibitor of S- adenosylhomocysteine hydrolase was synthesized from D-ribose, employing stereoselective hydroxymethylation, regioselective oxidation, and regio- and chemoselective hydroboration as key steps. Copyri