1395386-77-2

Upstream product

• 1166841-75-3 (R)-5-(tert-butyl-diphenyl-silanyloxymethyl)-cyclohex-2-enone 
• 1375467-36-9 (R)-3-(tert-butyldiphenylsilanyloxymethyl)-hex-5-enal 
• 1375467-38-1 (R)-5-(tert-butyldiphenylsilanyloxymethyl)-octa-1,7-dien-3-one 
• 1375467-47-2 C₂₉H₄₄O₃Si₂ 
• 1375467-35-8 (R)-3-(tert-butyldiphenylsilanyloxymethyl)-hex-5-enenitrile 

Downstream Products

• 1376197-50-0 (1S,2R,3R,5R)-5-(hydroxymethyl)cyclohexane-1,2,3-triol 

Relevant academic research and scientific papers

Stereoselective synthesis of a novel natural carbasugar and analogues from hydroxymethylated cycloalkenone scaffolds

Novel carbasugars from Streptomyces lincolnensis have been synthesized from an enantiomerically pure 5-hydroxymethyl-cyclohex-2-enone scaffold via a stereoselective approach. Several structural analogues of those carbasugars have also been synthesized in a stereoselective manner from hydroxymethylated cycloalkenone derivatives.