反应 #1365730

ord-39b2a81db9c64b418492bef4b0128491

反应方程式

O=C1C(=O)c2ccccc2-c2ccccc21
9,10-phenanthrenequinone
O=C1C(=O)c2c(ccc3ccccc23)-c2ccccc21
5,6-chrysenequinone

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

In a typical preparation, 50 mg of Rh(III) starting material was dissolved in 32 mL of MeCN/water, 3:1, 0.1 M in NaOH. To this mixture was added 1 equiv or more of 9,10-phenanthrenequinone (to produce non-hindered control DNA photocleaving compounds or 5,6-chrysenequinone (to produce hindered intercalating compounds). During constant stirring, the reaction was allowed to progress for approximately 18 h at room temperature. After neutralization with dilute hydrochloric acid and addition of 500 mL of water, the reaction mixture was loaded onto a Sephadex SP-C25 ion exchange column equilibrated in 0.05 M MgCl2. The product was purified by elution with a gradient of 0.05-0.5 M MgCl2, and the orange product bands were collected. The fractions were concentrated on a Waters Sep-Pak 5g C18 cartridge and washed with copious amounts of water. The metal complex was eluted from the cartridge with a minimum volume of 0.1% TFA in MeCN/water, 1:1, and lyophilized to dryness.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US06444661B1uspto-grants-2002_09