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Thioxanthen-9-one

The DszC enzyme was able to convert the following compounds other than DBT thioxanthen-9-one, 2,8-dimethyl DBT, 4,6-dimethyl DBT, and 3,4-benzo DBT. Non-organosulfur compounds such as biphenyl, carbazole, and dibenzofuran did not show any activity. This indicates that dszC specifically recognizes sulfur atom [151]. One study specifically examined the DszC enzyme for oxidation of aryl sulfides [179] and reported oxidation of many sulfides including, naphthyl methyl sulfide, phenyl methyl sulfide, and its alkyl derivatives. [Pg.101]

Thioxanthene-9-one [492-22-8] M 212.3, m 209 . Crystd from CHCI3 and sublimed in vacuo. [Pg.341]

Thioxanthen-9-one 10,10-dioxides with sodamide undergo ring expansion to dibenzo [/>,/]-[l,4]thiazepin-l 1-one 5,5-dioxides (75JHC1211). [Pg.665]

Figure 12 Bond lengths (pm) and bond angles (°) for 9H-thioxanthen-9-one 10,10-dioxide. Figure 12 Bond lengths (pm) and bond angles (°) for 9H-thioxanthen-9-one 10,10-dioxide.
Thioxanthen-9-ones. This base is somewhat superior to LDA for lithiation... [Pg.187]

The chemical structures of other compounds described in this chapter, namely, photosensitizers thioxanthene-9-one (TX) and 2-isopropyl thioxanthene-9-one (ITX), monomers isobornyl acrylate (IBOA), -butyl methacrylate (NBA), methyl acrylate (MA), vinyl acrylate (VA) and methyl methacrylate (MMA) are presented in Scheme 12.3. [Pg.256]

S YNS 1 -((2-(DlETHYLAMINO)ETHYL)AMINO)-4-METHYL-9H-THIOXANTHEN-9-ONE LUCANTHON LUCANTHONE MIRACIL D NILODIN... [Pg.482]

SYNS l-((2-piETHYLAMINO)ETHYL)AMINO)-4-(HYDROXYMETHYL)THIOX. 3NTHEN-9-ONE l-((2-piETHYLAMINO)ETHYL)AMINO)-4-(HYDROXYMETH-YL)9H-THIOXANTHEN-9-ONE HYCANTHON HYCANTHONE NSC-134434 WIN 24933... [Pg.846]

The ketyl radicals of thioxanthen-9-one (166) and -9-thione (167) have been described by several groups, and various ion-pairing phenomena were reported.The hyperfine splittings indicated in gauss, for the ion-pair of 166 with potassium in DME are those of Urberg and Kaiser, and those for the ion-pair of (167) with sodium in the same solvent are due to Aarons and Adam, who found a marked temperature dependence of the counterion hyperfine splittings that indicated is for 23°C. [Pg.98]

The conjugate acid of thioxanthen-9-one ketyl has been generated photolytically and characterized by both ESR and electronic absorption spectroscopy. ... [Pg.98]

The thioxanthen-9-one sulfoxide ketyl (169) has been obtained as its ion-pair with potassium in DME. Its hyperfine spectrum (splittings in... [Pg.98]

Horwitz, J.P., Massova, L, Wiese, T.E., Besler, B.H. and Corbett, T.H. (1994). Comparative Molecular Field Analysis of the Antitumor Activity of 9H-Thioxanthen-9-One Derivatives Against Pancreatic Ductal Carcinoma 03. J.Med.Chem., 37, 781-786. [Pg.586]

A solution containing 3-allyl-3-methyl-l,2-diphenylcyclopropene (100 mg, 0.41 mmol) and thioxanthen-9-one (100 mg) in benzene (150 mL) was irradiated under an argon atmosphere for 1 h with a 450-W Hanovia arc lamp equipped with a uranium glass filter sleeve. The mixture was concentrated under reduced pressure to a volume of approximately 10 mL and column chromatographed (silica gel, hexane). Removal of the solvent under reduced pressure left 70 mg (70%) of a colorless oil which was identified as the title compound. [Pg.206]


See other pages where Thioxanthen-9-one is mentioned: [Pg.368]    [Pg.369]    [Pg.324]    [Pg.91]    [Pg.635]    [Pg.635]    [Pg.369]    [Pg.206]    [Pg.731]    [Pg.827]    [Pg.924]    [Pg.187]    [Pg.851]    [Pg.1625]    [Pg.1625]    [Pg.264]    [Pg.519]    [Pg.98]    [Pg.368]    [Pg.369]    [Pg.635]    [Pg.307]    [Pg.448]    [Pg.765]    [Pg.868]    [Pg.868]    [Pg.870]    [Pg.938]    [Pg.945]    [Pg.295]   
See also in sourсe #XX -- [ Pg.187 ]




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