A facile synthesis of C2-symmetric 17β-estradiol dimers
- 1 February 2003
- journal article
- research article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 13 (3) , 557-560
- https://doi.org/10.1016/s0960-894x(02)00987-3
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- 2,5-Anhydro sugar diacid and 2,5-anhydro sugar diamine based C2 symmetric peptidomimetics as potential HIV-1 protease inhibitorsTetrahedron Letters, 2000
- Synthesis of C 2 -symmetric guanidino-sugars as potent inhibitors of glycosidasesBioorganic & Medicinal Chemistry, 2000
- Synthesis and Preliminary in Vitro Cytotoxic Activity of New Triphenylethylene DimersBioorganic Chemistry, 1999
- Synthesis of spermidine and norspermidine dimers as high affinity polyamine transport inhibitorsBioorganic & Medicinal Chemistry Letters, 1999
- Protective Groups in Organic SynthesisPublished by Wiley ,1999
- D-ring allyl derivatives of 17β- and 17α-estradiols: Chemical synthesis and 13C NMR dataSteroids, 1997
- Jozimine A (‘dimeric’ dioncophylline A), a non-natural michellamine analog with high antimalarial activityTetrahedron, 1996
- Opioid Antagonist Activity of Naltrexone-Derived Bivalent Ligands: Importance of a Properly Oriented Molecular Scaffold To Guide “Address” Recognition at κ Opioid ReceptorsJournal of Medicinal Chemistry, 1996
- Bivalent ligands as probes of estrogen receptor actionThe Journal of Steroid Biochemistry and Molecular Biology, 1994
- Prodrugs Utilizing Organosilyl Derivation: An Investigation of the Long-Term Androgenic and Myotrophic Activities of Silyl Derivatives of TestosteroneJournal of Pharmaceutical Sciences, 1988