Synthesis of 17α-substituted ethynylestradiols: Potential ligands for drug vectors
17α-substituted ethynylestradiols, derived from estrone, were converted to their corresponding 17α-(bromo- or iodo-propargyl)estrone intermediates. Nucleophilic substitution onto these moieties with malonate diester followed by hydrolysis and complexation with cis-Pt(Me 2en)I 2 (Me 2en = N, N-dimeth...
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Veröffentlicht in: | Steroids 2010-07, Vol.75 (7), p.489-498 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | 17α-substituted ethynylestradiols, derived from estrone, were converted to their corresponding 17α-(bromo- or iodo-propargyl)estrone intermediates. Nucleophilic substitution onto these moieties with malonate diester followed by hydrolysis and complexation with
cis-Pt(Me
2en)I
2 (Me
2en
=
N,
N-dimethylethylenediamine) gave
cis-Pt(Me
2en)(2-(3-(17β-estradiol-17α-yl)-prop-2-ynyl)malonato)
7, thus demonstrating that these estrogen-derived compounds can be used to synthesize stable Pt(II) complexes. The 3-(17β-estradiol-17α
-yl)-prop-2-ynyl-1-sulfanylethylthiol
23 was also prepared. |
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ISSN: | 0039-128X 1878-5867 |
DOI: | 10.1016/j.steroids.2010.03.004 |