1395294-08-2

Upstream product

• 42201-43-4 2-allyl-1,3-propanediol 
• 1375467-32-5 (R)-4-(tert-butyldiphenylsilanyloxymethyl)-hepta-1,6-dien-3-one 
• 1375467-31-4 4-(tert-butyldiphenylsilanyloxymethyl)-hepta-1,6-dien-3-ol 
• 1375467-30-3 (R)-2-(tert-butyldiphenylsilanyloxymethyl)-pent-4-enal 
• 1375467-29-0 (S)-2-(tert-butyldiphenylsilanyloxymethyl)-pent-4-en-1-ol 
• 1375467-50-7 (1S,2S,3R,5R)-3-(tert-butyldiphenylsilyloxymethyl)-6-oxa-bicyclo[3.1.0]hexan-2-ol 
• 1375467-48-3 (1R,5R)-5-(tert-butyldiphenylsilyloxymethyl)cyclopent-2-enol 
• 1375467-27-8 2-(((tert-butyldiphenylsilyl)oxy)methyl)pent-4-en-1-ol 

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.