217636-02-7

Upstream product

• 206185-21-9 (1R,4S)-4-methoxy-5,5-dimethylcyclopent-2-en-1-yl acetate 
• 167965-98-2 (1S,4R)-4-acetoxy-5,5-dimethyl-2-cyclopentene-1-ol 
• 100-39-0 benzyl bromide 
• 217636-01-6 (1R,4S)-4-Methoxy-5,5-dimethyl-cyclopent-2-enol 

Downstream Products

• 217636-05-0 C₂₉H₃₀O₆ 
• 217636-07-2 C₂₂H₂₂O₆ 
• 217636-06-1 C₂₂H₂₄O₆ 
• 217636-03-8 (1R,2S,3S,5R)-3-Benzyloxy-5-methoxy-4,4-dimethyl-cyclopentane-1,2-diol 

Relevant academic research and scientific papers

Enantiospecific total synthesis of (-)-D-noviose

(-)-D-Noviose ((-)-22), a rare sugar, was synthesized starting from the optically active building block (-)-1 in seven steps. The first step of this route, the introduction of a methyl-ether group under Lewis-acidic conditions, left the acetoxy group unto