TY - JOUR
T1 - Crystal structures of ()-(1SR,5SR,6SR,7SR,10SR,-11SR,13RS,14SR,15SR,16RS)-13-acetoxy-16-benz-yloxy-15-hydroxy-7-methoxymethoxy-3-oxo-11,15,18,18-tetramethyl-2,4-dioxatetracyclo-[12.3.1.01,5.06,11]octadecan-10-yl benzoate and its 13-epimer
AU - Oishi, Takeshi
AU - Fukaya, Keisuke
AU - Sato, Takaaki
AU - Chida, Noritaka
N1 - Publisher Copyright:
© 2025 International Union of Crystallography. All rights reserved.
PY - 2025/1/1
Y1 - 2025/1/1
N2 - The title compounds, C38H48O11 (A and B), are tetracyclic benzoates composed of a taxane ring with a fused dioxolane ring as the core skeleton. In compound A, the five-membered dioxolane ring is essentially planar while the two cyclohexane rings and the cyclooctane ring adopt chair and chair–chair forms, respectively, and there are three intramolecular H H short contacts. The corresponding ring conformations in B are similar; however, one intramolecular C—H O interaction and two H H short contacts are observed, and the benzoyl and methoxymethyl groups show orientational disorder. In the crystal of A, a pair of intermolecular O—H O hydrogen bonds link two molecules into an inversion dimer, and weak intermolecular C—H O interactions connect the dimers, forming a three-dimensional network. In the crystal of B, an inversion dimer is similarly generated by a pair of intermolecular O—H O hydrogen bonds, and weak intermolecular C—H O and C—H π interactions connect the dimers into a three-dimensional architecture.
AB - The title compounds, C38H48O11 (A and B), are tetracyclic benzoates composed of a taxane ring with a fused dioxolane ring as the core skeleton. In compound A, the five-membered dioxolane ring is essentially planar while the two cyclohexane rings and the cyclooctane ring adopt chair and chair–chair forms, respectively, and there are three intramolecular H H short contacts. The corresponding ring conformations in B are similar; however, one intramolecular C—H O interaction and two H H short contacts are observed, and the benzoyl and methoxymethyl groups show orientational disorder. In the crystal of A, a pair of intermolecular O—H O hydrogen bonds link two molecules into an inversion dimer, and weak intermolecular C—H O interactions connect the dimers, forming a three-dimensional network. In the crystal of B, an inversion dimer is similarly generated by a pair of intermolecular O—H O hydrogen bonds, and weak intermolecular C—H O and C—H π interactions connect the dimers into a three-dimensional architecture.
KW - crystal structure
KW - disorder
KW - hydrogen bond
KW - paclitaxel
KW - taxane skeleton
UR - https://www.scopus.com/pages/publications/85214439252
UR - https://www.scopus.com/inward/citedby.url?scp=85214439252&partnerID=8YFLogxK
U2 - 10.1107/S2056989024012234
DO - 10.1107/S2056989024012234
M3 - Article
AN - SCOPUS:85214439252
SN - 2056-9890
VL - 81
SP - 74
EP - 79
JO - Acta Crystallographica Section E: Crystallographic Communications
JF - Acta Crystallographica Section E: Crystallographic Communications
IS - Pt 1
ER -