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2. Oxidation of Cymantrene Analogues of Ferrocifen: Electrochemical, Spectroscopic, and Computational Studies of the Parent Complex 1,1′-Diphenyl-2-cymantrenylbutene
3. A New Series of Succinimido-ferrociphenols and Related Heterocyclic Species Induce Strong Antiproliferative Effects, Especially against Ovarian Cancer Cells Resistant to Cisplatin
4. Evidence for Targeting Thioredoxin Reductases with Ferrocenyl Quinone Methides. A Possible Molecular Basis for the Antiproliferative Effect of Hydroxyferrocifens on Cancer Cells
5. Oxidative Sequence of a Ruthenocene-Based Anticancer Drug Candidate in a Basic Environment
6. Synthesis, Characterization, and Antiproliferative Activities of Novel Ferrocenophanic Suberamides against Human Triple-Negative MDA-MB-231 and Hormone-Dependent MCF-7 Breast Cancer Cells
7. Synthesis and Antiproliferative Effects of [3]Ferrocenophane Transposition Products and Pinacols Obtained from McMurry Cross-Coupling Reactions
8. Synthetic and Mechanistic Pathways of Cis and Trans-Hydroxytamoxifen Drug Derivatives Reacting with Cp*Rh Complexes that involve η1-N, η2-N,O, η1-O, and η6 Bonding Modes, via a Novel N-π Rearrangement; Relative Binding Affinities and Computer Docking Studies of Cis and Trans-η6-Cp*Rh-Hydroxytamoxifen Complexes at the Estrogen, ERα and ERβ Receptors, and Growth Inhibition to Breast Cancer Cells
9. Synthesis and Structure Activity Relationship of Organometallic Steroidal Androgen Derivatives
10. Synthesis and Structure–Activity Relationships of the First Ferrocenyl-Aryl-Hydantoin Derivatives of the Nonsteroidal Antiandrogen Nilutamide
11. Comparative Oxidative Addition of Transition-Metal Iodocyclopentadienyl Complexes (η5-C5H4-I)MLn (M = Re, Mn, Fe) with a Palladium(0) Complex: Relevance to the Efficiency of Catalytic Reactions
12. New Ortho-Directing Group for Lithiation: Use of a Methoxy−Imino Auxiliary for the Synthesis of Chiral Ortho-Substituted Acetyl- and Propionylferrocenes
13. Synthesis of Optically Pure o-Formylcyclopentadienyl Metal Complexes of 17α-Ethynylestradiol. Recognition of the Planar Chirality by the Estrogen Receptor
14. New Synthetic Pathways of cis- or trans-Hydroxytamoxifen Derivatives with in Situ Formed [Cp*Rh(solvent)3]2+ Complexes: Kinetic and Thermodynamic Control, Including a Novel, Intramolecular N-π Rearrangement, and Relative Binding Affinities of the η6 Complexes for the Estrogen Receptor
15. Modification of the Estrogenic Properties of Diphenols by the Incorporation of Ferrocene. Generation of Antiproliferative Effects in Vitro
16. Selective Estrogen Receptor Modulators in the Ruthenocene Series. Synthesis and Biological Behavior
17. Decomplexation of Cyclopentadienylmanganese Tricarbonyls under Very Mild Conditions: A Novel Route to Substituted Cyclopentadienes and Their Application in Organometallic Synthesis
18. A Novel and Mild Metal-Exchange Reaction in the Organometallic Cyclopentadienyl Series: 1,1‘-Diaryl 2-Cymantrenyl 1-Butene as an Example
19. Diels−Alder Dimerization of Cyclopenta[l]phenanthrene (Dibenz[e,g]indene) with Isodibenzindene: A Computational, NMR Spectroscopic, and X-ray Crystallographic Study
20. Organometallics as Potential Protein Labels: Pyrylium and Pyridinium Salts Bearing (C6H5)Cr(CO)3, (C5H4)Mn(CO)3, and Ferrocenyl Substituents
21. Rhenium Carbonyl Complexes of .beta.-Estradiol Derivatives with High Affinity for the Estradiol Receptor: An Approach to Selective Organometallic Radiopharmaceuticals
22. [.eta.5-Cyclopentadienyl]metal Tricarbonyl Pyrylium Salts: Novel Reagents for the Specific Conjugation of Proteins with Transition Organometallic Labels
23. Ionization of (.eta.6-diphenylmethane)(.eta.5-cyclopentadienyl)iron cations in H2O-Me2SO and methanol-Me2SO mixtures: a kinetic, NMR, and EHMO study
24. Labeling of proteins by organometallic complexes of rhenium(I). Synthesis and biological activity of the conjugates
25. Protonation of chromium tricarbonyl complexes of triphenylsilanol and triphenylcarbinol: synthetic, x-ray crystallographic, and NMR study of (Ph3SiOH)[Cr(CO)3]n (n = 1-3) and of (Ph3COH)Cr(CO)3
26. Molecular recognition using bioorganometallic probes: NMR, x-ray crystallographic, and molecular modeling study of the conformations of chromium tricarbonyl derivatives of hexestrol and their relevance to estradiol-receptor binding
27. Syntheses and affinities of novel organometallic-labeled estradiol derivatives: a structure-affinity relationship
28. Synthetic, structural, and reactivity studies of dirhenium carbonyl complexes of 17.alpha.-ethynylestradiol and phenylacetylene: variable-temperature carbon-13 NMR spectra and x-ray crystal structure of (.mu.-H)(.mu.-C.tplbond.C-R)Re2(CO)7(MeCN)
29. An x-ray crystallographic and high-field NMR study of chromium complexes [(C6Et6)Cr(CO)2NO]+BF4- and [(C6Et6)Cr(CO)(CS)NO]+BF4-: steric inhibition of tripodal rotation
30. Diamagnetic anisotropy of organometallic moieties: .chi. values for M(CO)3 (M = Cr, Mo, W) and for ferrocene
31. Organometallic estrogens: synthesis, interaction with lamb uterine estrogen receptor, and detection by infrared spectroscopy
32. N-Alkylation of nitriles using chromium tricarbonyl complexes of benzyl alcohol and its derivatives: new perspectives for the Ritter reaction
33. Transition-metal carbonyl clusters as novel infrared markers for estradiol receptor site detection
34. Regiospecific and stereospecific functionalization of benzylic sites by tricarbonylchromium arene complexation
35. Transition-metal carbonyl complexes in progesterone receptor assay
36. Chromium tricarbonyl complexes of estradiol derivatives: differentiation of .alpha.- and .beta.-diastereoisomers using 1- and 2-dimensional NMR spectroscopy at 500 MHz
37. Metal carbonyl fragments as a new class of markers in molecular biology
38. Rotational barriers in diphenylmethyl anions stabilized by trimethylsilyl and tricarbonylchromium(0) moieties
39. Relative acidifying effects of tricarbonylchromium(0) and p-nitro groups upon di- and triphenylmethanes
40. Electrochemical differentiation of .alpha.- and .beta.-diastereoisomers of the steroid hormone receptor marker 3-(benzyloxy)-17.beta.-hydroxyestra-1,3,5(10)-trienetricarbonylchromium
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