TY - JOUR
T1 - Ethyl 5-(5-oxo-2,3-dihydro-5H-oxazolo[2,3-a]-isoindol-9b-ylmethyl)-4-(2,5, 5-trimethyl-1,3-dioxan-2-yl)isoxazole-3-carboxylate
T2 - The product of a novel synthetic method
AU - Nelson, Jared
AU - Twamley, Brendan
AU - Natale, Nicholas R.
PY - 2004/12
Y1 - 2004/12
N2 - The title compound, C24H28N2O7, is the product of a novel synthetic procedure in which a highly functionalized heterocycle is formed. The crystal packing involves dimers, utilizing non-classical weak C-H⋯O interactions (ca 3.36-3.46 Å) and an antiparallel π-π interaction between two of the pseudo-aromatic isoxazole moieties. These dimers are associated into a three-dimensional network via further nonclassical hydrogen bonding.
AB - The title compound, C24H28N2O7, is the product of a novel synthetic procedure in which a highly functionalized heterocycle is formed. The crystal packing involves dimers, utilizing non-classical weak C-H⋯O interactions (ca 3.36-3.46 Å) and an antiparallel π-π interaction between two of the pseudo-aromatic isoxazole moieties. These dimers are associated into a three-dimensional network via further nonclassical hydrogen bonding.
UR - http://www.scopus.com/inward/record.url?scp=18444401443&partnerID=8YFLogxK
U2 - 10.1107/S1600536804027655
DO - 10.1107/S1600536804027655
M3 - Article
AN - SCOPUS:18444401443
SN - 1600-5368
VL - 60
SP - o2255-o2257
JO - Acta Crystallographica Section E: Structure Reports Online
JF - Acta Crystallographica Section E: Structure Reports Online
IS - 12
ER -