140835-86-5

Upstream product

• 140835-65-0 (1R^*,2S^*,3S^*,4R^*,5S^*)-1,2:5,6-diepoxy-4-hydroxy-5-isopropyl-3-methylhexyl N,N-diisopropylcarbamate 
• 140835-72-9 <2R^*,3S^*,4R^*,5(2S^*)>-tetrahydro-3-hydroxy-5-(2-isopropyloxiran-2-yl)-4-methylfuran-2-yl N,N-diisopropylcarbamate 
• 140835-63-8 (1Z,3R^*,4R^*)-4-hydroxy-5-isopropyl-3-methylhexa-1,5-dienyl N,N-diisopropylcarbamate 
• 4417-80-5 3-methyl-2-methylene-butyraldehyde 
• 591-51-5 phenyllithium 
• 140835-76-3 <4R^*,6S^*,6(1R^*),7R^*,8R^*>-6-(2-isopropyloxiran-2-yl)-2,2,7-trimethyl-1,3,5-trioxabicyclo<3.3.0>octane 

Relevant academic research and scientific papers

Diastereo-and Enantioselective Synthesis of 1,2:5,6-Diepoxy-4-hydroxyalkyl Carbamates. - Regioselective Ring Opening and Their Transformation into Doubly C-Branched Deoxy Sugar Analogues

Enantiomerically enriched (Z)-anti-3,5-dialkyl-4-hydroxy-1,5-alkadienyl N,N-diisopropylcarbamates 12, readily obtained by the homoaldol approach, were oxidized with essentially complete diastereoselectivity to afford 1,2:5,6-diepoxides 14 of D-allo config