Synthesis and redox behavior of new ferrocene- π-extended- dithiafulvalenes: An approach for anticipated organic conductors

• Abdelwareth A. O. Sarhan,
• Omar F. Mohammed and
• Taeko Izumi

Beilstein J. Org. Chem. 2009, 5, No. 6, doi:10.3762/bjoc.5.6

• . 1H NMR and 13C NMR spectra were recorded at room temperature on a Varian Nuclear Magnetic Resonance Spectrometer (500 MHz). Chemical shifts are denoted in δ units (ppm), relative to tetramethylsilane (TMS) as internal standard, J values are given in Hz. MS and FAB-MS spectra were obtained using a

Colchitaxel, a coupled compound made from microtubule inhibitors colchicine and paclitaxel

• Karunananda Bombuwala,
• Thomas Kinstle,
• Vladimir Popik,
• Sonal O. Uppal,
• James B. Olesen,
• Jose Viña and
• Carol A. Heckman

Beilstein J. Org. Chem. 2006, 2, No. 13, doi:10.1186/1860-5397-2-13

• Proton Nuclear Magnetic Resonance. Supporting Information File 40: VRO showing microtubule + ends localized by antibody against EB1 in a control cell. Part of the VRO is rendered in a two-dimensional form in Figure 2. Control cells were treated with solvent vehicle only. Note that + ends of microtubules