TY - JOUR
T1 - An ortho-rhom-bic polymorph of 6-de-oxy-6-iodo-1,2
T2 - 3,4-di-O-isopropyl-idene - D-galactopyran-oside
AU - Fun, Hoong Kun
AU - Liew, Wei Ching
AU - Rai, Sankappa
AU - Shetty, Prakash
AU - Isloor, Arun M.
PY - 2009/8/20
Y1 - 2009/8/20
N2 - The title compound, C12H19IO5, is the ortho-rhom-bic polymorph of a previously reported monoclinic form [Krajewski et al. (1987). Bull. Pol. Acad. Sci. Chem. 35, 91-102]. The dihedral angles between the six-membered ring and the two five-membered rings are 67.66 (14) and 71.79 (13)°, whereas the dihedral angle between the five-membered rings is 74.41 (12)°, indicating that all three rings are twisted from each other. The six-membered ring has a twist-boat conformation while both of the five-membered rings have envelope conformations. The crystal structure is stabilized by a network of C - H⋯O contacts linking the mol-ecules into a two-dimensional array parallel to the ab plane.
AB - The title compound, C12H19IO5, is the ortho-rhom-bic polymorph of a previously reported monoclinic form [Krajewski et al. (1987). Bull. Pol. Acad. Sci. Chem. 35, 91-102]. The dihedral angles between the six-membered ring and the two five-membered rings are 67.66 (14) and 71.79 (13)°, whereas the dihedral angle between the five-membered rings is 74.41 (12)°, indicating that all three rings are twisted from each other. The six-membered ring has a twist-boat conformation while both of the five-membered rings have envelope conformations. The crystal structure is stabilized by a network of C - H⋯O contacts linking the mol-ecules into a two-dimensional array parallel to the ab plane.
UR - http://www.scopus.com/inward/record.url?scp=68749093985&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=68749093985&partnerID=8YFLogxK
U2 - 10.1107/S1600536809029031
DO - 10.1107/S1600536809029031
M3 - Article
AN - SCOPUS:68749093985
SN - 1600-5368
VL - 65
JO - Acta Crystallographica Section E: Structure Reports Online
JF - Acta Crystallographica Section E: Structure Reports Online
IS - 8
ER -