1094382-79-2

Upstream product

• 4132-26-7 2,3,4,6-tetra-O-benzyl 1,5-anhydro-D-arabino-hex-1-enitol 
• 67-66-3 chloroform 

Downstream Products

• 1094383-30-8 1-azido-1-deoxy-2-chloro-2-deoxy-3,4,5,7-tetra-O-benzyl-D-arabino-hept-2-enoseptanoside 
• 1094383-17-1 methyl O-(2-chloro-2-deoxy-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-enoseptanosyl)-(1->5)-2,3-di-O-benzyl-α-D-arabinofuranoside 
• 1094383-19-3 methyl O-(2-chloro-2-deoxy-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-enoseptanosyl)-(1->6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside 
• 1094382-81-6 phenyl 2-chloro-2-deoxy-3,4,5,7-tetra-O-benzyl-D-arabino-hept-2-enoseptanoside 
• 1608472-02-1 n-pentyl 2-chloro-2-deoxy-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-eno-septanoside 
• 1608472-12-3 acetyl 2-chloro-2-deoxy-3,4,5,7-tetra-O-benzyl-α-D-arabinohept-2-enoseptanoside 
• 1608472-10-1 ((2-hydroxyethoxy)ethyl)-2-chloro-2-deoxy-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-enoseptanoside 
• 1608472-06-5 allyl 2-chloro-2-deoxy-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-enoseptanoside 
• 1608472-11-2 benzyl 2-chloro-2-deoxy-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-enoseptanoside 
• 1608472-09-8 isopropyl 2-chloro-2-deoxy-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-enoseptanoside 
• 1608472-07-6 propargyl 2-chloro-2-deoxy-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-enoseptanoside 
• 1608472-04-3 n-nonayl 2-chloro-2-deoxy-3,4,5,7-tetra-O-benzyl-α-D-arabino-hept-2-enoseptanoside 

Relevant academic research and scientific papers

Dense network of O-H?O and C-H?O interactions in the solid state structure of n-pentyl-2-chloro-2-deoxy-α-d-manno-sept 3-uloside

Single crystal X-ray structural analysis of a septanoside, namely, n-pentyl-2-chloro-2-deoxy sept-3-uloside (1) provides many finer details of the molecular structure, in addition to its preferred twist-chair conformation, namely, 5,6TC3,4 conformation. Structural analysis reveals a dense network of OH-O, CH-O and van der Waals interactions that stabilize interdigitized, planar bi-layer structure of the crystal lattice.

Glycosidic bond hydrolysis in septanosides: A comparison of mono-, di-, and 2-chloro-2-deoxy-septanosides

A kinetic study of the hydrolytic stabilities of mono-, di-, and 2-chloro-2-deoxy septanosides, under acid-catalysis, is reported herein. A comparison of mono- and diseptanosides, shows that the glycosidic bond in the disaccharide is more stable than the

Exclusive ring opening of gem-dihalo-1,2-cyclopropanated oxyglycal to oxepines in AgOAc

Treatment of gem-dihalo-1,2-cyclopropanated d-oxyglycal with primary, secondary, and unsaturated alcohols, in the presence of AgOAc, leads to the formation of chloro-oxepines exclusively. Reaction of the resulting 2-chloro-oxepines with excess alcohol in

Synthesis of aryl, glycosyl, and azido septanosides through ring expansion of 1,2-cyclopropanated sugars

A ring-expansion methodology for the preparation of aryl septanosides, arabinofuranosyl and glucopy- ranosyl septanoside disaccharides, and azido septanosides is reported. A cyclopropanated adduct of the oxyglycal upon reaction with phenols, sugars, and a