321126-15-2

Upstream product

• 180067-18-9 C₃₆H₄₉F₃O₆ 
• 100-39-0 benzyl bromide 
• 107108-67-8 tert-butyl 2,3-deoxy-α-D-glucopyranoside 
• 107108-66-7 Acetic acid (2R,3S,6R)-2-acetoxymethyl-6-tert-butoxy-tetrahydro-pyran-3-yl ester 
• 69247-20-7 tert-butyl 4,6-di-O-acetyl-2,3-dideoxy-α-D-erythrohex-2-enopyranoside 
• 167901-78-2 2,2,2-trifluoroethyl 4-O-benzyl-2,3,6,7,8,9-hexadeoxy-α-D-erythro-non-8-enopyranoside 
• 167901-83-9 tert-butyl 4-O-benzyl-2,3,6,7,8,9-hexadeoxy-α-D-threo-non-8-enopyranoside 
• 321126-18-5 3-((2R,3R,6R)-3-Benzyloxy-6-tert-butoxy-tetrahydro-pyran-2-yl)-propionaldehyde 
• 321126-29-8 3-[(2R,3S,6S)-3-Benzyloxy-6-(2,2,2-trifluoro-ethoxy)-tetrahydro-pyran-2-yl]-propionaldehyde 
• 321126-20-9 (2R,3S,6S)-3-Benzyloxy-2-(3-iodo-propyl)-6-(2,2,2-trifluoro-ethoxy)-tetrahydro-pyran 
• 321126-24-3 trifluoroethyl 4-O-benzyl-2,3,6,7-tetradeoxy-α-D-gluco-octopyranoside 
• 190188-69-3 Toluene-4-sulfonic acid (2R,3S,6R)-6-tert-butoxy-3-hydroxy-tetrahydro-pyran-2-ylmethyl ester 
• 321126-28-7 trifluoroethyl 2,3-dideoxy-α-D-gluco-pyranoside 
• 321126-19-6 2,2,2-trifluoroethyl?4,6-di-O-acetyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside 

Downstream Products

• 180186-85-0 C₃₆H₄₉F₃O₆ 
• 180067-21-4 (2S,5R,2'S,5'R)-5'-((R)-1-Benzyloxy-pent-4-enyl)-5-((S)-1-benzyloxy-pent-4-enyl)-octahydro-[2,2']bifuranyl 
• 321126-25-4 (2R,3S,6S)-3-Benzyloxy-2-{(R)-3-[(2S,5R)-5-((R)-1-benzyloxy-pent-4-enyl)-tetrahydro-furan-2-yl]-3-iodo-propyl}-6-(2,2,2-trifluoro-ethoxy)-tetrahydro-pyran 
• 180067-20-3 (R)-4-Benzyloxy-4-((2R,5S)-5-{(R)-3-[(2R,3S,6S)-3-benzyloxy-6-(2,2,2-trifluoro-ethoxy)-tetrahydro-pyran-2-yl]-1-iodo-propyl}-tetrahydro-furan-2-yl)-butyraldehyde 
• 180186-89-4 (R)-4-Benzyloxy-4-((2R,5R)-5-{(R)-3-[(2R,3S,6S)-3-benzyloxy-6-(2,2,2-trifluoro-ethoxy)-tetrahydro-pyran-2-yl]-1-iodo-propyl}-tetrahydro-furan-2-yl)-butyraldehyde 

Relevant academic research and scientific papers

A modular synthesis of the bis-tetrahydrofuran core of rolliniastatin from pyranoside precursors

The iodoetherification of C6 allyllated 2,3-dideoxypyranosides has been shown to give cis-2,5-disubstituted tetrahydrofurans in high stereoselectivity. This result is applied to a modular synthesis of the bis-THF core of the acetogenin, rolliniastatin. (C) 2000 Elsevier Science Ltd.

Bis-pyranoside alkenes: Novel templates for the synthesis of adjacently linked tetrahydrofurans

Bis-pyranoside alkenes are used as templates for the convergent assembly of highly substituted, adjacently linked, tetrahydrofurans (THF's). The methodology centers on the stereoselective preparation of a bis-THF diol core structure.