40983-95-7

Usage

InChI:InChI=1/C27H28O6/c28-23-24-22(18-31-26(33-24)21-14-8-3-9-15-21)32-27(30-17-20-12-6-2-7-13-20)25(23)29-16-19-10-4-1-5-11-19/h1-15,22-28H,16-18H2/t22?,23-,24+,25?,26?,27-/m0/s1

Upstream product

• 40983-94-6 (4aR,6S,7S,8R,8aS)-6-benzyloxy-2-phenyl-4,4a,6,7,8,8a-hexahydropyrano[5,6-d][1,3]dioxine-7,8-diol 
• 100-39-0 benzyl bromide 
• 58650-53-6 benzyl endo-2,3:4,6-di-O-benzylidene-α-D-mannopyranoside 
• 100-51-6 benzyl alcohol 
• 100-52-7 benzaldehyde 
• 15548-45-5 (2S,3S,4S,5S,6R)-2-benzyloxy-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol 
• 7296-15-3 alpha-D-mannopyranoside 

Downstream Products

• 58527-92-7 benzyl 3-O-allyl-2,4-di-O-benzyl-α-D-mannopyranoside 
• 86342-16-7 benzyl 3-O-allyl-2,4-di-O-benzyl-α-D-rhamnopyranoside 
• 86342-18-9 benzyl 2,4-di-O-benzyl-α-D-rhamnopyranoside 
• 86342-14-5 benzyl 3-O-allyl-2,4-di-O-benzyl-6-O-(p-toluenesulfonyl)-α-D-mannopyranoside 
• 69401-46-3 benzyl 2,4-di-O-benzyl-α-D-mannopyranoside 
• 81600-94-4 benzyl 2-O-benzyl-3-O-(tetra-O-acetyl-α-D-mannopyranosyl)-4,6-benzylidene-α-D-mannopyranoside 
• 53929-39-8 benzyl 3-O-allyl-2-O-benzyl-4,6-benzylidene-α-D-mannopyranoside 

Relevant academic research and scientific papers

MANNOSE DERIVATIVES FOR TREATING BACTERIAL INFECTIONS

The present invention relates to compounds useful for the treatment or prevention of bacteria infections. These compounds have formula I: The invention also provides processes for making the compounds described herein. Furthermore, the present invention p

CHEMO-, STEREO- AND REGIOSELECTIVE HYDROGENOLYSIS OF CARBOHYDRATE BENZYLIDENE ACETALS. SYNTHESIS OF BENZYL ETHERS OF BENZYL α-D-, METHYL β-D-MANNOPYRANOSIDES AND BENZYL α-D-RHAMNOPYRANOSIDE BY RING CLEAVAGE OF BENZYLIDENE DERIVATIVES WITH THE LiAlH4-AlCl3

Treatment of benzyl α-(1) and methyl β-D-mannopyranoside (2) with α,α-dimethoxytoluene gave the exo and endo isomers (3,5 and 4,6) of the dibenzylidene derivatives of 1 and 2.Hydrogenolysis of the exo isomers (3 and 5) with a molar equivalent of AlH2Cl ga