Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

© Springer Science+Business Media New York 2015. 2-Azido-4-aminocyclohexane-1,3-diols 12, 14 and 16 were synthesised and their crystal structures were studied by X-ray diffraction. Compound 12 crystallizes in the monoclinic space group P2 1 /n with cell parameters of a = 13.7059(2) Å, b = 10.8861(2) Å, c = 13.8675(3) Å, β = 117.2365(10)°, V = 1839.67(6) Å3 and Z = 4. Compound 14 crystallizes in the orthorhombic space group Pcab with cell parameters of a = 9.9508(1) Å, b = 10.9839(2) Å, c = 24.7035(4) Å, V = 2700.06(7) Å3 and Z = 8. Compound 16 crystallizes in the triclinic space group P1 P 1 ¯ with cell parameters of a = 10.9511(3) Å, b = 11.3148(3) Å, c = 15.9545(5) Å, α = 86.3487(11)°, β = 87.4723(11)°, γ = 89.3398(10)°, V = 1970.91(10) Å3 and Z = 4. All three structures were characterised by arrays of hydrogen bonding interactions and these crystallographic studies also revealed their conformations, which gave valuable information into the regioselectivity of epoxide ring-opening during their formation.

Original publication

DOI

10.1007/s10870-015-0607-x

Type

Journal article

Journal

Journal of Chemical Crystallography

Publication Date

30/09/2015

Volume

45

Pages

401 - 409