86972-02-3

Upstream product

• 33106-64-8 (S)-2-(benzyloxy)propan-1-ol 
• 81445-44-5 (S)-2-(benzyloxy)propanal 
• 77896-97-0 2-<(E)-3-methoxy-2-propenyl>-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 86972-01-2 2-((Z)-3-Methoxy-allyl)-4,5-dimethyl-[1,3,2]dioxaborolane 

Downstream Products

• 86972-06-7 (3S,4S,5S)-4,5-Bis(benzyloxy)-3-methoxyhexanal 
• 86972-13-6 Benzyl 2-O-<α-Ethoxy-α-(trifluoromethyl)phenylacetyl>-β-L-oleandroside 
• 86972-07-8 Benzyl L-Oleandroside 
• 86972-07-8 benzyl 2-deoxy-3-O-methyl-α-L-rhamnopyranoside 
• 86972-08-9 Benzyl L-Oleandroside (α anomer) 
• 86972-09-0 Benzyl 4-O-Acetyl-L-oleandroside 
• 86972-09-0 Benzyl 4-O-Acetyl-L-oleandroside (β anomer) 
• 86972-10-3 Benzyl 4-O-Acetyl-L-oleandroside (α anomer) 
• 87037-66-9 (3R,4R,5S)-4,5-Bis-benzyloxy-3-methoxy-hexan-1-ol 
• 87037-65-8 (3R,4S,5S)-4,5-Bis-benzyloxy-3-methoxy-hexan-1-ol 
• 86972-04-5 (3S,4S,5S)-4,5-Bis(benzyloxy)-3-methoxyhexanol 
• 87037-63-6 C₂₁H₂₆O₃ 
• 86972-03-4 (3S,4S,5S)-4,5-Bis(benzyloxy)-3-methoxy-1-hexene 
• 87037-64-7 C₂₁H₂₆O₃ 

Relevant academic research and scientific papers

Stereoselective Syntheses of Alcohols, XXIV. - Synthesis of 2,6-Dideoxy-L-hexoses

Addition of the Z- and E-γ-alkoxyallylboronates 3 and 6 to O-benzyllactaldehyde led to various 3,4,5-trioxygenated 1-hexenes of arabino, xylo, ribo and lyxo configuration.The extent of asymmetric induction amounted to 82:18 (arabino/xylo) in the addition