145306-82-7

Upstream product

• 145229-56-7 (2R,6S)-1,7-Bis-benzyloxy-hept-3-yne-2,6-diol 
• 2930-05-4 (S)-benzyl glycidyl ether 
• 85428-24-6 (R)-4-benzyloxy-3-hydroxy-1-butyne 
• 145306-80-5 (2R,6R)-1,7-Bis-benzyloxy-hept-3-yne-2,6-diol 
• 14618-80-5 (R)-benzyl glycidol 
• 60656-87-3 benzyloxyacetoaldehyde 
• 169517-16-2 2-allenyl-[1,3,2]-dioxaborinane 

Downstream Products

• 145229-61-4 (R)-1-Benzyloxy-3-[(2S,3R)-3-((S)-2-benzyloxy-1-hydroxy-ethyl)-oxiranyl]-propan-2-ol 
• 145229-61-4 (S)-1-Benzyloxy-3-[(2R,3S)-3-((S)-2-benzyloxy-1-hydroxy-ethyl)-oxiranyl]-propan-2-ol 
• 145229-61-4 (R)-1-Benzyloxy-3-[(2R,3S)-3-((S)-2-benzyloxy-1-hydroxy-ethyl)-oxiranyl]-propan-2-ol 
• 145229-61-4 (S)-1-Benzyloxy-3-[3-((S)-2-benzyloxy-1-hydroxy-ethyl)-oxiranyl]-propan-2-ol 
• 145229-61-4 (R)-1-Benzyloxy-3-[3-((S)-2-benzyloxy-1-hydroxy-ethyl)-oxiranyl]-propan-2-ol 
• 145229-59-0 (R)-1-Benzyloxy-3-((2R,4R,6R)-6-benzyloxymethyl-2-phenyl-[1,3]dioxan-4-yl)-propan-2-ol 
• 145229-59-0 (S)-1-Benzyloxy-3-((2R,4R,6R)-6-benzyloxymethyl-2-phenyl-[1,3]dioxan-4-yl)-propan-2-ol 
• 145229-60-3 (2R,4R,6S)-1,7-Bis-benzyloxy-heptane-2,4,6-triol 
• 145229-60-3 (2R,6R)-1,7-Bis-benzyloxy-heptane-2,4,6-triol 
• 145229-62-5 (2S,3R,6R)-1,7-Bis-benzyloxy-heptane-2,3,6-triol 
• 145229-60-3 (2S,4S,6R)-1,7-Bis-benzyloxy-heptane-2,4,6-triol 
• 145229-62-5 (2S,3R,6S)-1,7-Bis-benzyloxy-heptane-2,3,6-triol 
• 145229-62-5 (2S,3S,6S)-1,7-Bis-benzyloxy-heptane-2,3,6-triol 

Relevant academic research and scientific papers

Enantioselective synthesis of 1,5-anti- and 1,5-syn-diols using a highly diastereoselective one-pot double allylboration reaction sequence

Highly diastereo- and enantioselective syntheses of 1,5-disubstituted (E)-1,5-anti-pent-2-endiols 1 and (Z)-1,5-syn-pent-2-endiols 2 have been achieved via the one-pot coupling of two different aldehydes with either (E)-γ-(1,3,2-dioxaborinanyl)-allyl]diis

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