A Convergent, Enantioselective Total Synthesis of Hapalosin: A Drug with Multidrug-Resistance Reversing Activity
- 19 January 1996
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 35 (1) , 74-76
- https://doi.org/10.1002/anie.199600741
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Potent HIV protease inhibitors: the development of tetrahydrofuranylglycines as novel P2-ligands and pyrazine amides as P3-ligandsJournal of Medicinal Chemistry, 1993
- Synthesis and antiviral activity of a series of HIV-1 protease inhibitors with functionality tethered to the P1 or P1' phenyl designJournal of Medicinal Chemistry, 1992
- Multidrug ResistanceAnnual Review of Medicine, 1991
- THE BIOCHEMISTRY OF P-GLYCOPROTEIN-MEDIATED MULTIDRUG RESISTANCEAnnual Review of Biochemistry, 1989
- Verapamil and adriamycin in the treatment of drug-resistant ovarian cancer patients.Journal of Clinical Oncology, 1987
- Cell Surface P-Glycoprotein Associated with Multidrug Resistance in Mammalian Cell LinesScience, 1983