97189-80-5

Upstream product

• 60656-87-3 benzyloxyacetoaldehyde 
• 58931-16-1 1-(benzyloxy)-4-penten-2-ol 

Downstream Products

• 1262957-82-3 1,5-bis(benzyloxy)pentane-2,4-diol 
• 1262957-89-0 C₁₉H₂₀O₂S 
• 1262957-85-6 2,4-bis(benzoyloxymethyl)thietane 
• 122040-29-3 2-[(1R,2S,5R)-1-((1S,3R)-4-Benzyloxy-1-benzyloxymethyl-3-hydroxy-butoxy)-2-isopropyl-5-methyl-cyclohexyl]-1-phenyl-ethanone 
• 122040-14-6 2-[(1R,2S,5R)-1-((S)-2-(R)-1,4-Dioxa-spiro[4.5]dec-2-yl-1-hydroxymethyl-ethoxy)-2-isopropyl-5-methyl-cyclohexyl]-1-phenyl-ethanone 
• 122040-24-8 (2S,4R,6R,7S,10R)-2,4-Bis-benzyloxymethyl-7-isopropyl-10-methyl-1,5-dioxa-spiro[5.5]undecane 
• 122040-19-1 C₂₅H₄₀O₄Si₂ 
• 122040-13-5 2-[(1R,2S,5R)-1-((1S,3R)-3,4-Dihydroxy-1-hydroxymethyl-butoxy)-2-isopropyl-5-methyl-cyclohexyl]-1-phenyl-ethanone 
• 122040-33-9 (2S,4R)-1,5-Bis-benzyloxy-4-methoxymethoxy-pentan-2-ol 

Relevant academic research and scientific papers

Synthesis of thietane nucleoside with an anomeric hydroxymethyl group

Thietane nucleoside 5 with an anomeric hydroxymethyl group was synthesized via the Pummerer reaction. The stereochemistry of the sulfoxide and the nature of the protecting group had no significant effect on the yield of the reaction. When a hypervalent iodine reagent was used, sulfide 16 with O-benzoyl protecting groups gave the ring-expanded nucleoside 21. Unfortunately, synthesized compound 6 did not exhibit anti-HSV activity. Copyright

CYCLIC LIPID DERIVATIVES AS POTENT PAF ANTAGONISTS

The present invention describes novel cyclic diol derivatives represented by formula I and II: STR1 in which Y represents O, S, SO, SO 2, (CH 2) m wherein m is zero or an integer of 1 to 5, or NR a group wherein R a is hydrogen, lower alkyl, lower alkoxyc

ENANTIODIFFERENTIATING FUNCTIONALIZATION OF meso-1,3-DIOLS VIA SPIROACETALS DERIVED FROM l-MENTHONE

Enantiodifferentiating functionalization of meso-1,3-diols is realized by the utilization of titanium tetrachloride-promoted selective ring-cleavage reaction of spiroacetals derived from l-menthone.