145229-59-0

Upstream product

• 14618-80-5 (R)-benzyl glycidol 
• 145306-80-5 (2R,6R)-1,7-Bis-benzyloxy-hept-3-yne-2,6-diol 
• 145229-56-7 (2R,6S)-1,7-Bis-benzyloxy-hept-3-yne-2,6-diol 
• 145306-82-7 (2R,6R,3E)-1,7-dibenzyloxyhept-3-ene-2,6-diol 
• 145306-83-8 (Z)-(2R,6R)-1,7-Bis-benzyloxy-hept-3-ene-2,6-diol 
• 145229-57-8 (E)-(2R,6S)-1,7-Bis-benzyloxy-hept-3-ene-2,6-diol 
• 145229-61-4 (R)-1-Benzyloxy-3-[(2R,3S)-3-((S)-2-benzyloxy-1-hydroxy-ethyl)-oxiranyl]-propan-2-ol 
• 145229-61-4 (R)-1-Benzyloxy-3-[(2S,3R)-3-((S)-2-benzyloxy-1-hydroxy-ethyl)-oxiranyl]-propan-2-ol 
• 145229-58-9 (R)-1-Benzyloxy-3-[2-((R)-3-benzyloxy-2-hydroxy-propyl)-[1,3]dithian-2-yl]-propan-2-ol 
• 392230-13-6 (2R)-1-benzyloxy-3-[1,3]dithian-2-yl-propan-2-ol 
• 85428-24-6 (R)-4-benzyloxy-3-hydroxy-1-butyne 
• 2930-05-4 (S)-benzyl glycidyl ether 
• 100-52-7 benzaldehyde 
• 145229-60-3 (2R,6R)-1,7-Bis-benzyloxy-heptane-2,4,6-triol 

Downstream Products

• 145229-60-3 (2R,4R,6S)-1,7-Bis-benzyloxy-heptane-2,4,6-triol 

Relevant academic research and scientific papers

Katsuki-Sharpless asymmetric epoxidation of allylic-homoallylic alcohols sharing the central olefinic bond

Katsuki-Sharpless asymmetric epoxidation of four isomeric chiral allylic-homoallylic diols sharing the central olefinic bond has been examined. Among these, three heptenediols having (3E,2R,6R), (3E,2R,6S), and (3Z,2R,6R) configurations underwent diastere