Kinetics and mechanism of the reaction of hydrogen peroxide with thiolato complexes of cobalt(III) and chromium(III). Comments on the nucleophilicity of coordinated sulfur and the stability of coordinated sulfenic acids
First Examples of Oxidizing Aldehydes to Carboxylic Acids in the Presence of a Tertiary Disulfide Functional Group: Synthesis of Novel Diacid-disulfides
作者:Xinqin Fang、Upul K. Bandarage、Tiansheng Wang、Joseph D. Schroeder、David S. Garvey
DOI:10.1055/s-2003-37518
日期:——
The disulfide functionality exists in numerous organic compounds of interest in both chemistry and biology. In view of the fact that the disulfide function is highly susceptible to further oxidation by a broad range of agents, conducting a chemoselective oxidation without further oxidizing the disulfide group poses a synthetic challenge. Disclosed herein are the first examples of such an oxidation in which a series of aldehyde disulfides (1a-e) were converted to the corresponding symmetrical carboxylic acid disulfides (2a-e), utilizing sodium chlorite as the oxidant, and dimethyl sulfoxide as both a reaction solvent and an efficient hypochlorous acid scavenger.
Purified cytotoxic proteins for use within therapeutic compositions are disclosed. The proteins inhibit protein synthesis in vitro, exhibit abortifacient activity in mice, and contain proline residues with equivalent positions at residue 43 and residue 46 in ricin A-chain. A method for preparing such a cytotoxic protein from the tissue of Trichosanthes kirilowii is also disclosed. The proteins may also be used as active therapeutic substances, such as within a method for inhibiting protein synthesis in selected cells.
本研究公开了用于治疗组合物的纯化细胞毒性蛋白质。这些蛋白质在体外抑制蛋白质合成,在小鼠体内表现出堕胎活性,并含有与蓖麻毒素 A 链中残基 43 和残基 46 位置相当的脯氨酸残基。还公开了一种从 Trichosanthes kirilowii 组织中制备这种细胞毒性蛋白质的方法。这些蛋白质还可用作活性治疗物质,例如用于抑制选定细胞中蛋白质合成的方法。
Process for the removal of hydrogen sulfide and optionally carbon dioxide from gaseous streams
申请人:THE DOW CHEMICAL COMPANY
公开号:EP0279667A2
公开(公告)日:1988-08-24
Hydrogen sulfide and/or carbon dioxide are removed from a sour gaseous stream in a contact zone by contacting the sour gaseous stream with H₂S- and/or CO₂- selective absorbent in an aqueous alkaline solution containing a polyvalent metal chelate at a pH of 7 to 10 wherein polyvalent metal chelate is in one embodiment of the invention in the reduced or lower valence state in a contact zone and is oxidized to the oxidized or higher valence state in an oxidation zone so as to convert hydrosulfide and/or sulfide salts present in the contact zone to sulfur. In a second embodiment, the aqueous alkaline solution and H₂S- and/or CO₂- selective absorbent in contact with the gaseous stream is a mixture containing a higher valence polyvalent metal chelate together with a lower valence polyvalent metal chelate, which lower valence polyvalent metal chelate is present in at least about five times the amount of the higher valence polyvalent metal chelant.
465. Carbon–sulphur fission in thioethers. Part VI. The structural factors leading to either carbanion–sulphenium fission or α-proton extraction in p-nitrophenylmethylthio-acids
作者:Youssef Iskander、Youssef Riad
DOI:10.1039/jr9610002397
日期:——
Tananger, Arkiv foer Kemi, 1947, vol. 24 A, # 10, p. 4