852610-46-9

Upstream product

• 852610-41-4 (3S,4S)-3,4-dihydroxymethyl-1-cyclopentene 
• 100-39-0 benzyl bromide 
• 852610-43-6 (1S,2S,3S,5R)-2,3-bis[(benzyloxy)methyl]-6-oxabicyclo[3.1.0]hexane 
• 852610-44-7 (1R,4S,5S)-4,5-bis[(benzyloxy)methyl]cyclopent-2-en-1-ol 
• 852610-42-5 (3S,4S)-bis(benzyloxymethyl)-1-cyclopentene 
• 852610-38-9 methyl (1S,2S)-2-[(2'S)-1',4'-dioxaspiro[4.5]dec-2'-yl]cyclopent-3-ene-1-carboxylate 
• 852610-52-7 (1S,2S)-2-((S)-1,2-Dihydroxy-ethyl)-cyclopent-3-enecarboxylic acid methyl ester 
• 852610-39-0 methyl (1S,2S)-2-formylcyclopent-3-ene-1-carboxylate 
• 852610-59-4 4-Nitro-benzoic acid (1R,4S,5S)-4,5-bis-benzyloxymethyl-cyclopent-2-enyl ester 

Downstream Products

• 852610-47-0 C₂₁H₂₃N₃O₂ 

Relevant academic research and scientific papers

Convenient route to both enantiomers of a highly functionalized trans-disubstituted cyclopentene. Synthesis of the carbocyclic core of the nucleoside BCA

Synthesis of both enantiomers of a highly functionalized cyclopentenol derivative, versatile building block for a vast array of biologically active compounds, is described. The key steps involve stereocontrolled synthesis of a diene with two syn-disposed