81408-36-8

Upstream product

• 3761-92-0 n-hexylmagnesium bromide 
• 81445-44-5 (S)-2-(benzyloxy)propanal 
• 81408-50-6 (2S)-2-(benzyloxy)-3-nonanone 
• 104101-26-0 (2S,3S)-2-Benzyloxy-7,7-bis-phenylsulfanyl-nonan-3-ol 
• 93367-11-4 (2S,3S)-3-benzyloxy-1,2-epoxybutane 
• 4613-16-5 5-O-benzyl-L-rhamnitol 
• 81408-34-6 (S)-2-Benzyloxy-nonan-3-ol 
• 4697-98-7 5-O-benzyl-1,2:3,4-di-O-isopropylidene-L-rhamnitol 
• 100-44-7 benzyl chloride 
• 104079-62-1 (S)-1-((S)-6-Ethyl-6-phenylsulfanyl-tetrahydro-pyran-2-yl)-ethanol 
• 104101-25-9 Methanesulfonic acid (1S,5S,7S)-5-ethyl-6,8-dioxa-bicyclo[3.2.1]oct-7-ylmethyl ester 
• 104079-60-9 (S)-2-Ethyl-6-(S)-oxiranyl-2-phenylsulfanyl-tetrahydro-pyran 
• 104079-56-3 Methanesulfonic acid (S)-2-((S)-6-ethyl-6-phenylsulfanyl-tetrahydro-pyran-2-yl)-2-hydroxy-ethyl ester 
• 53346-05-7 2-(benzyloxy)propanal 

Downstream Products

• 81408-34-6 (2S,3R)-2-O-benzyl-2,3-nonanediol 
• 81408-35-7 Methanesulfonic acid (R)-1-((S)-1-benzyloxy-ethyl)-heptyl ester 
• 81408-37-9 (2S,3S)-2-O-benzyl-3-O-methanesulfonyl-2,3-nonanediol 
• 81408-44-8 (2S,3R)-3-(adenin-9-yl)-2-O-benzyl-2-nonanol 
• 81408-42-6 (2S,3S)-3-(adenin-9-yl)-2-O-benzyl-2-nonanol 
• 93367-14-7 (2S,3R)-2-benzyloxy-3-hydrazononane 
• 81408-50-6 (2S)-2-(benzyloxy)-3-nonanone 

Relevant academic research and scientific papers

SYNTHESIS OF CHIRAL 1,2-DIOLS AND RELATED COMPOUNDS OF BIOLOGICAL ACTIVITIES VIA STEPWISE RING FISSION OF 5-ALKYL-6,8-DIOXABICYCLOOCTANE SKELETON

5-Alkyl-7-mesyloxymethyl-6,8-dioxabicyclooctanes, prepared from (+)-tartaric acid, were converted by means of an organoaluminium reagent Et2AlSPh into the pyranoid monothioacetals, which were utilized via the successive thioacetalization

ZnBr2-MEDIATED HIGHLY DIASTEREOSELECTIVE ADDITION OF GRIGNARD REAGENTS TO α-BENZYLOXY ALDEHYDES

α-Benzyloxy aldehydes reacted with Grignard reagents in the presence of ZnBr2 to afford vicinal syn-diol derivatives with high diastereoselectivity.

Synthesis of Inhibitors of Adenosine Deaminase. A Total Synthesis of erythro-3-(Adenin-9-yl)-2-nonanol and Its Isomers from Chiral Precursors

The synthesis of both isomers of EHNA2 ("erythrohydroxynonyladenine") from D- and L-rhamnose is described.The key intermediates, (R)- and (S)-2-(benzyloxy)propanal, derived respectively from 5-O-benzyl-D- and -L-rhamnitol, were each condensed w