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Carotid Artery Infusions for Pharmacokinetic and Pharmacodynamic Analysis of Taxanes in Mice
Published on: October 27, 2014
The oxetane conformational lock of paclitaxel: structural analysis of D-secopaclitaxel
T C Boge1, M Hepperle, D G Vander Velde
1Department of Medicinal Chemistry, University of Kansas, Lawrence 66045, USA.
Bioorganic & Medicinal Chemistry Letters
|November 26, 1999
Abstract:
Analysis of the 1H NMR data of paclitaxel in comparison with its oxetane ring-opened analogue D-secopaclitaxel suggests that the oxetane moiety (D-ring) of paclitaxel serves as a conformational lock for the diterpene moiety and the C13 side chain.
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