Isopropyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyran­oside

The title compound, C₁₇H₂₆O₁₀, was formed by a Koenigs–Knorr reaction of 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide and propan-2-ol. The central ring adopts a chair conformation. The crystal does not contain any significant inter­molecular inter­actions.

n-Propyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyran­oside

The title compound [systematic name: (2R,3R,4S,5R,6R)-2-(acet­oxy­meth­yl)-6-propoxytetra­hydro-2H-pyran-3,4,5-triyl triacetate], C₁₇H₂₆O₁₀, was formed by a Koenigs–Knorr reaction of 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide and n-propanol. The central ring adopts a chair conformation. The crystal does not contain any significant inter­actions such as hydrogen bonds.

1-(4-Bromo-3,5,5,6,8,8-hexa­methyl-5,6,7,8-tetra­hydro­naphthalen-2-yl)ethan-1-one: a precursor for phase-I metabolite of AHTN

The title compound, C₁₈H₂₅BrO, crystallized as a racemate with four independent mol­ecules in the asymmetric unit. In the crystal, three of these four mol­ecules are linked via C—Br...Br—C halogen bonds [Br...Br = 3.662 (2) and 3.652 (2) Å], forming dimers.