98497-46-2

Upstream product

• 98497-30-4 S,S-(+)-4-hydroxy-5-(2-trityloxy-ethyl)-2-cyclopentenone 
• 98497-29-1 (+)-3,4-β-epoxy-2β-(2-trityloxy-ethyl)-cyclopentanone 
• 98497-28-0 (+)-3,4-β-epoxy-2β-(2-trityloxy-ethyl)-cyclopentan-1β-ol 
• 98497-27-9 (+)-2β-(2-trityloxy-ethyl)-3-cyclopenten-1β-ol 
• 54483-54-4 (+)-2β-hydroxyethyl-3-cyclopenten-1β-ol 
• 34638-25-0 (1R,5S)-2-oxabicyclo[3.3.0]oct-6-en-3-one 

Downstream Products

• 98497-48-4 4-methoxy-2-(2-trityloxy-ethyl)-2-cyclopentenone 
• 98497-50-8 3-methoxy-2-(2-trityloxy-ethyl)-2-cyclopentenone 
• 115058-93-0 (+/-)-3-methoxy-5-(2-trityloxy-ethyl)-2-cyclopentenone 
• 98497-47-3 (S)-4-(tert-Butyl-dimethyl-silanyloxy)-2-(2-trityloxy-ethyl)-cyclopent-2-enone 

Relevant academic research and scientific papers

Novel molecular rearrangements of 4-hydroxy-2-cyclopentenones

Novel rearrangements of hydroxycyclopentenone derivatives 1 and 24 to 7,9,11 and 31,33,35 are reported. The stereochemistry of the rearrangement is interpreted as the result of synchronous enolate induced [1.5]-sigmatropic rearrangement and stepwise addition-elimination process. Preparation of the various substrates and structural elucidation of new products are also described.