62774-16-7

Usage

Chemical Properties

Colorless Oil

InChI:InChI=1/C27H28O6/c28-23-25(29-16-19-10-4-1-5-11-19)24-22(18-31-26(33-24)21-14-8-3-9-15-21)32-27(23)30-17-20-12-6-2-7-13-20/h1-15,22-28H,16-18H2/t22?,23?,24-,25-,26?,27+/m1/s1

Upstream product

• 58650-53-6 benzyl exo-2,3:4,6-di-O-benzylidene-α-D-mannopyranoside 
• 65529-49-9 benzyl 2,3(R):4,6(R)-di-O-benzylidene-α-D-mannopyranoside 
• 15548-45-5 (2S,3S,4S,5S,6R)-2-benzyloxy-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol 
• 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 
• 100-51-6 benzyl alcohol 
• 530-26-7 D-Mannose 

Downstream Products

• 23346-01-2 4,6-O-Benzylidene-1,2-dideoxy-D-erythro-hex-1-enopyranos-3-ulose 
• 72869-11-5 benzyl 4,6-O-benzylidene-2-deoxy-α-D-erythro-hexopyranosid-3-ulose 
• 121237-34-1 benzyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-erythro-hex-2-enopyranoside 
• 121237-33-0 (4aR,6S,7R,8S,8aR)-6,8-Bis-benzyloxy-7-chloro-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 121237-37-4 (4aR,6S,7R,8S,8aR)-6,8-Bis-benzyloxy-7-bromo-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 121237-38-5 (4aR,6S,7R,8S,8aR)-6,8-Bis-benzyloxy-7-iodo-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxine 
• 121237-35-2 Benzoic acid (4aR,6S,7R,8S,8aR)-6,8-bis-benzyloxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl ester 
• 865488-85-3 C₃₄H₄₃NO₁₄ 
• 865488-86-4 benzyl 4,6-di-O-acetyl-3-O-benzyl-2-O-[3,4,6-tri-O-acetyl-2-acetamido-2-deoxy-β-D-glucopyranosyl]-α-D-mannopyranoside 
• 865488-96-6 2-(p-iodophenyl)ethyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl-(1->2)-3,4,6-tri-O-acetyl-α-D-mannopyranosyl-(1->6)-2,3,4-tri-O-acetyl-β-D-glucopyranoside 
• 865488-97-7 2-(p-iodophenyl)ethyl 2-acetamido-2-deoxy-β-D-glucopyranosyl-(1->2)-α-D-mannopyranosyl-(1->6)-β-D-glucopyranoside 
• 865488-98-8 benzyl 3-O-benzyl-2-O-[3,4,6-tri-O-acetyl-2-deoxy-2-(N-phthalimido)-β-D-glucopyranosyl]-α-D-mannopyranoside 
• 865488-99-9 benzyl 3-O-benzyl-6-O-tert-butyldimethylsilyl-2-O-[3,4,6-tri-O-acetyl-2-deoxy-2-(N-phthalimido)-β-D-glucopyranosyl]-α-D-mannopyranoside 
• 865489-00-5 benzyl 4-O-acetyl-3-O-benzyl-6-O-tert-butyldimethylsilyl-2-O-[3,4,6-tri-O-acetyl-2-deoxy-2-(N-phthalimido)-β-D-glucopyranosyl]-α-D-mannopyranoside 

Relevant academic research and scientific papers

INHIBITORS OF HEXOKINASE AND METHODS OF USE THEREOF

Provided herein are substituted substituted heterocycles useful as inhibitors of the HKII enzyme. The invention further provides pharmaceutical compositions of the compounds of the invention. The invention further provides medical uses of substituted heterocycles, for example, as antitumor agents.

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

Synthesis of a Tri-, a Penta-, and a Hepta-saccharide Containing Terminal N-Acetyl-β-D-lactosaminyl Residues, Part of the 'Complex-type' Carbohydrate Moiety of Glycoproteins

Silver trifluoromethanesulphonate-promoted condensation of 3,6-di-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-2-deoxy-2-phthalimido-β-D-glucopyranosyl bromide with benzyl 3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside, benzyl 3,6-di-O-ben