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Showing 25 to 36 of 72 entries
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Switching the Switch: Ligand Induced Disulfide Formation in HDAC8.

Chemistry (Weinheim an der Bergstrasse, Germany)

Jänsch N, Sugiarto WO, Muth M, Kopranovic A, Desczyk C, Ballweg M, Kirschhöfer F, Brenner-Weiss G, Meyer-Almes FJ.
PMID: 32428298
Chemistry. 2020 Oct 15;26(58):13249-13255. doi: 10.1002/chem.202001712. Epub 2020 Sep 11.

Human histone deacetylase 8 is a well-recognized target for T-cell lymphoma and particularly childhood neuroblastoma. PD-404,182 was shown to be a selective covalent inhibitor of HDAC8 that forms mixed disulfides with several cysteine residues and is also able to...

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Jänsch N, Sugiarto WO, Muth M, et al. Switching the Switch: Ligand Induced Disulfide Formation in HDAC8. Chemistry. 2020;26(58):13249-13255doi: 10.1002/chem.202001712.
Jänsch, N., Sugiarto, W. O., Muth, M., Kopranovic, A., Desczyk, C., Ballweg, M., Kirschhöfer, F., Brenner-Weiss, G., & Meyer-Almes, F. J. (2020). Switching the Switch: Ligand Induced Disulfide Formation in HDAC8. Chemistry (Weinheim an der Bergstrasse, Germany), 26(58), 13249-13255. https://doi.org/10.1002/chem.202001712
Jänsch, Niklas, et al. "Switching the Switch: Ligand Induced Disulfide Formation in HDAC8." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 26,58 (2020): 13249-13255. doi: https://doi.org/10.1002/chem.202001712
Jänsch N, Sugiarto WO, Muth M, Kopranovic A, Desczyk C, Ballweg M, Kirschhöfer F, Brenner-Weiss G, Meyer-Almes FJ. Switching the Switch: Ligand Induced Disulfide Formation in HDAC8. Chemistry. 2020 Oct 15;26(58):13249-13255. doi: 10.1002/chem.202001712. Epub 2020 Sep 11. PMID: 32428298; PMCID: PMC7692948.
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Synthesis of (benzenesulfonyl)difluoromethyl thioethers from ((difluoromethyl)sulfonyl)benzene and organothiocyanates generated .

Organic & biomolecular chemistry

Wu C, Shen X, Dai J, Xu J, Xu H.
PMID: 34524317
Org Biomol Chem. 2021 Sep 15;19(35):7607-7610. doi: 10.1039/d1ob01215k.

Easily available aryl and alkyl thiocyanates were converted into the corresponding (benzenesulfonyl)difluoromethyl thioethers

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Wu C, Shen X, Dai J, et al. Synthesis of (benzenesulfonyl)difluoromethyl thioethers from ((difluoromethyl)sulfonyl)benzene and organothiocyanates generated . Org Biomol Chem. 2021;19(35):7607-7610doi: 10.1039/d1ob01215k.
Wu, C., Shen, X., Dai, J., Xu, J., & Xu, H. (2021). Synthesis of (benzenesulfonyl)difluoromethyl thioethers from ((difluoromethyl)sulfonyl)benzene and organothiocyanates generated . Organic & biomolecular chemistry, 19(35), 7607-7610. https://doi.org/10.1039/d1ob01215k
Wu, Cheng, et al. "Synthesis of (benzenesulfonyl)difluoromethyl thioethers from ((difluoromethyl)sulfonyl)benzene and organothiocyanates generated ." Organic & biomolecular chemistry vol. 19,35 (2021): 7607-7610. doi: https://doi.org/10.1039/d1ob01215k
Wu C, Shen X, Dai J, Xu J, Xu H. Synthesis of (benzenesulfonyl)difluoromethyl thioethers from ((difluoromethyl)sulfonyl)benzene and organothiocyanates generated . Org Biomol Chem. 2021 Sep 15;19(35):7607-7610. doi: 10.1039/d1ob01215k. PMID: 34524317.
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Phenol-containing macrocyclic diamides as new catalysts in the highly regioselective conversion of epoxides to beta-hydroxy thiocyanates.

The Journal of organic chemistry

Sharghi H, Nasseri MA, Niknam K.
PMID: 11681940
J Org Chem. 2001 Nov 02;66(22):7287-93. doi: 10.1021/jo0103266.

The regioselective ring-opening reactions of some epoxides with ammonium thiocyanate in the presence of a series of new phenol-containing macrocyclic diamides and also dibenzo-18-crown-6-, 18-crown-6-, benzo-15-crown-5-, and pyridine-containing macrocyclic diamide have been studied. The epoxides were subject to cleavage...

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Sharghi H, Nasseri MA, Niknam K. Phenol-containing macrocyclic diamides as new catalysts in the highly regioselective conversion of epoxides to beta-hydroxy thiocyanates. J Org Chem. 2001;66(22):7287-93doi: 10.1021/jo0103266.
Sharghi, H., Nasseri, M. A., & Niknam, K. (2001). Phenol-containing macrocyclic diamides as new catalysts in the highly regioselective conversion of epoxides to beta-hydroxy thiocyanates. The Journal of organic chemistry, 66(22), 7287-93. https://doi.org/10.1021/jo0103266
Sharghi, H, et al. "Phenol-containing macrocyclic diamides as new catalysts in the highly regioselective conversion of epoxides to beta-hydroxy thiocyanates." The Journal of organic chemistry vol. 66,22 (2001): 7287-93. doi: https://doi.org/10.1021/jo0103266
Sharghi H, Nasseri MA, Niknam K. Phenol-containing macrocyclic diamides as new catalysts in the highly regioselective conversion of epoxides to beta-hydroxy thiocyanates. J Org Chem. 2001 Nov 02;66(22):7287-93. doi: 10.1021/jo0103266. PMID: 11681940.
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Reduction of Aryl Thiocyanates with SmI(2) and Pd-Catalyzed Coupling with Aryl Halides as a Route to Mixed Aryl Sulfides.

The Journal of organic chemistry

Still IW, Toste FD.
PMID: 11667721
J Org Chem. 1996 Nov 01;61(22):7677-7680. doi: 10.1021/jo961029h.

A series of aryl iodides, with a range of substituents, has been successfully coupled using 10 mol % Pd catalyst with samarium thiolates, derived from the corresponding aryl thiocyanates upon reductive cleavage with SmI(2). Reactions proceed in THF at...

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Still IW, Toste FD. Reduction of Aryl Thiocyanates with SmI(2) and Pd-Catalyzed Coupling with Aryl Halides as a Route to Mixed Aryl Sulfides. J Org Chem. 1996;61(22):7677-7680doi: 10.1021/jo961029h.
Still, I. W., & Toste, F. D. (1996). Reduction of Aryl Thiocyanates with SmI(2) and Pd-Catalyzed Coupling with Aryl Halides as a Route to Mixed Aryl Sulfides. The Journal of organic chemistry, 61(22), 7677-7680. https://doi.org/10.1021/jo961029h
Still, Ian W. J., and Toste, F. Dean. "Reduction of Aryl Thiocyanates with SmI(2) and Pd-Catalyzed Coupling with Aryl Halides as a Route to Mixed Aryl Sulfides." The Journal of organic chemistry vol. 61,22 (1996): 7677-7680. doi: https://doi.org/10.1021/jo961029h
Still IW, Toste FD. Reduction of Aryl Thiocyanates with SmI(2) and Pd-Catalyzed Coupling with Aryl Halides as a Route to Mixed Aryl Sulfides. J Org Chem. 1996 Nov 01;61(22):7677-7680. doi: 10.1021/jo961029h. PMID: 11667721.
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Revisiting nucleophilic substitution reactions: microwave-assisted synthesis of azides, thiocyanates, and sulfones in an aqueous medium.

The Journal of organic chemistry

Ju Y, Kumar D, Varma RS.
PMID: 16901176
J Org Chem. 2006 Aug 18;71(17):6697-700. doi: 10.1021/jo061114h.

A practical, rapid, and efficient microwave (MW) promoted synthesis of various azides, thiocyanates, and sulfones is described in an aqueous medium. This general and expeditious MW-enhanced nucleophilic substitution approach uses easily accessible starting materials such as halides or tosylates...

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Ju Y, Kumar D, Varma RS. Revisiting nucleophilic substitution reactions: microwave-assisted synthesis of azides, thiocyanates, and sulfones in an aqueous medium. J Org Chem. 2006;71(17):6697-700doi: 10.1021/jo061114h.
Ju, Y., Kumar, D., & Varma, R. S. (2006). Revisiting nucleophilic substitution reactions: microwave-assisted synthesis of azides, thiocyanates, and sulfones in an aqueous medium. The Journal of organic chemistry, 71(17), 6697-700. https://doi.org/10.1021/jo061114h
Ju, Yuhong, et al. "Revisiting nucleophilic substitution reactions: microwave-assisted synthesis of azides, thiocyanates, and sulfones in an aqueous medium." The Journal of organic chemistry vol. 71,17 (2006): 6697-700. doi: https://doi.org/10.1021/jo061114h
Ju Y, Kumar D, Varma RS. Revisiting nucleophilic substitution reactions: microwave-assisted synthesis of azides, thiocyanates, and sulfones in an aqueous medium. J Org Chem. 2006 Aug 18;71(17):6697-700. doi: 10.1021/jo061114h. PMID: 16901176.
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Selective determination of cyanides by gas diffusion-stopped flow-sequential injection analysis and an on-line standard addition approach.

Analytica chimica acta

Themelis DG, Karastogianni SC, Tzanavaras PD.
PMID: 19100887
Anal Chim Acta. 2009 Jan 19;632(1):93-100. doi: 10.1016/j.aca.2008.10.074. Epub 2008 Nov 06.

A highly selective sequential injection (SI) method for the automated determination of weak-acid-dissociable cyanides is reported. The analytical procedure is based on the on-line reaction of the analyte with ninhydrin in carbonate medium to form a coloured product (lambda(max)=510...

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Themelis DG, Karastogianni SC, Tzanavaras PD. Selective determination of cyanides by gas diffusion-stopped flow-sequential injection analysis and an on-line standard addition approach. Anal Chim Acta. 2008;632(1):93-100doi: 10.1016/j.aca.2008.10.074.
Themelis, D. G., Karastogianni, S. C., & Tzanavaras, P. D. (2009). Selective determination of cyanides by gas diffusion-stopped flow-sequential injection analysis and an on-line standard addition approach. Analytica chimica acta, 632(1), 93-100. https://doi.org/10.1016/j.aca.2008.10.074
Themelis, Demetrius G, et al. "Selective determination of cyanides by gas diffusion-stopped flow-sequential injection analysis and an on-line standard addition approach." Analytica chimica acta vol. 632,1 (2009): 93-100. doi: https://doi.org/10.1016/j.aca.2008.10.074
Themelis DG, Karastogianni SC, Tzanavaras PD. Selective determination of cyanides by gas diffusion-stopped flow-sequential injection analysis and an on-line standard addition approach. Anal Chim Acta. 2009 Jan 19;632(1):93-100. doi: 10.1016/j.aca.2008.10.074. Epub 2008 Nov 06. PMID: 19100887.
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Neutral complexes of first row transition metals bearing unbound thiocyanates and their assembly on metallic surfaces.

Journal of the American Chemical Society

Ciszek JW, Keane ZK, Cheng L, Stewart MP, Yu LH, Natelson D, Tour JM.
PMID: 16522098
J Am Chem Soc. 2006 Mar 15;128(10):3179-89. doi: 10.1021/ja055459d.

A series of transition metal coordination complexes designed to assemble on gold surfaces was synthesized, their electronic structure and transitions analyzed, and their magnetic properties studied. By taking advantage of recently developed thiocyanate assembly protocols, these molecules were then...

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Ciszek JW, Keane ZK, Cheng L, et al. Neutral complexes of first row transition metals bearing unbound thiocyanates and their assembly on metallic surfaces. J Am Chem Soc. 2006;128(10):3179-89doi: 10.1021/ja055459d.
Ciszek, J. W., Keane, Z. K., Cheng, L., Stewart, M. P., Yu, L. H., Natelson, D., & Tour, J. M. (2006). Neutral complexes of first row transition metals bearing unbound thiocyanates and their assembly on metallic surfaces. Journal of the American Chemical Society, 128(10), 3179-89. https://doi.org/10.1021/ja055459d
Ciszek, Jacob W, et al. "Neutral complexes of first row transition metals bearing unbound thiocyanates and their assembly on metallic surfaces." Journal of the American Chemical Society vol. 128,10 (2006): 3179-89. doi: https://doi.org/10.1021/ja055459d
Ciszek JW, Keane ZK, Cheng L, Stewart MP, Yu LH, Natelson D, Tour JM. Neutral complexes of first row transition metals bearing unbound thiocyanates and their assembly on metallic surfaces. J Am Chem Soc. 2006 Mar 15;128(10):3179-89. doi: 10.1021/ja055459d. PMID: 16522098.
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About a synthetic saliva for in vitro studies.

Talanta

Gal JY, Fovet Y, Adib-Yadzi M.
PMID: 18968202
Talanta. 2001 Mar 16;53(6):1103-15. doi: 10.1016/s0039-9140(00)00618-4.

Numerous artificial salivas have been used during studies in odontology. These salivas have compositions, which are more or less the same as that of natural saliva. In this article, we are presenting a discussion about the various media described...

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Gal JY, Fovet Y, Adib-Yadzi M. About a synthetic saliva for in vitro studies. Talanta. 2001;53(6):1103-15doi: 10.1016/s0039-9140(00)00618-4.
Gal, J. Y., Fovet, Y., & Adib-Yadzi, M. (2001). About a synthetic saliva for in vitro studies. Talanta, 53(6), 1103-15. https://doi.org/10.1016/s0039-9140(00)00618-4
Gal, J Y, et al. "About a synthetic saliva for in vitro studies." Talanta vol. 53,6 (2001): 1103-15. doi: https://doi.org/10.1016/s0039-9140(00)00618-4
Gal JY, Fovet Y, Adib-Yadzi M. About a synthetic saliva for in vitro studies. Talanta. 2001 Mar 16;53(6):1103-15. doi: 10.1016/s0039-9140(00)00618-4. PMID: 18968202.
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Anion-exchange studies of metal thiocyanates in aqueous and mixed solvent systems.

Talanta

Singh D, Tandon SN.
PMID: 18962404
Talanta. 1979 Feb;26(2):163-5. doi: 10.1016/0039-9140(79)80240-4.

The anion-exchange behaviour of metal ions in aqueous NH(4)CNS and aqueous NH(4)CNS-organic solvent mixtures has been studied. The effect of the pH and the concentrations of thiocyanate and organic solvent on the distribution coefficients has been investigated. Fifteen binary...

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Singh D, Tandon SN. Anion-exchange studies of metal thiocyanates in aqueous and mixed solvent systems. Talanta. 1979;26(2):163-5doi: 10.1016/0039-9140(79)80240-4.
Singh, D., & Tandon, S. N. (1979). Anion-exchange studies of metal thiocyanates in aqueous and mixed solvent systems. Talanta, 26(2), 163-5. https://doi.org/10.1016/0039-9140(79)80240-4
Singh, D, and Tandon, S N. "Anion-exchange studies of metal thiocyanates in aqueous and mixed solvent systems." Talanta vol. 26,2 (1979): 163-5. doi: https://doi.org/10.1016/0039-9140(79)80240-4
Singh D, Tandon SN. Anion-exchange studies of metal thiocyanates in aqueous and mixed solvent systems. Talanta. 1979 Feb;26(2):163-5. doi: 10.1016/0039-9140(79)80240-4. PMID: 18962404.
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Fluorescence spectroscopic studies of (acetamide + sodium/potassium thiocyanates) molten mixtures: composition and temperature dependence.

The journal of physical chemistry. B

Guchhait B, Gazi HA, Kashyap HK, Biswas R.
PMID: 20345185
J Phys Chem B. 2010 Apr 22;114(15):5066-81. doi: 10.1021/jp1001176.

Steady state and time-resolved fluorescence spectroscopic techniques have been used to explore the Stokes' shift dynamics and rotational relaxation of a dipolar solute probe in molten mixtures of acetamide (CH(3)CONH(2)) with sodium and potassium thiocyanates (Na /KSCN) at T...

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Guchhait B, Gazi HA, Kashyap HK, et al. Fluorescence spectroscopic studies of (acetamide + sodium/potassium thiocyanates) molten mixtures: composition and temperature dependence. J Phys Chem B. 2010;114(15):5066-81doi: 10.1021/jp1001176.
Guchhait, B., Gazi, H. A., Kashyap, H. K., & Biswas, R. (2010). Fluorescence spectroscopic studies of (acetamide + sodium/potassium thiocyanates) molten mixtures: composition and temperature dependence. The journal of physical chemistry. B, 114(15), 5066-81. https://doi.org/10.1021/jp1001176
Guchhait, Biswajit, et al. "Fluorescence spectroscopic studies of (acetamide + sodium/potassium thiocyanates) molten mixtures: composition and temperature dependence." The journal of physical chemistry. B vol. 114,15 (2010): 5066-81. doi: https://doi.org/10.1021/jp1001176
Guchhait B, Gazi HA, Kashyap HK, Biswas R. Fluorescence spectroscopic studies of (acetamide + sodium/potassium thiocyanates) molten mixtures: composition and temperature dependence. J Phys Chem B. 2010 Apr 22;114(15):5066-81. doi: 10.1021/jp1001176. PMID: 20345185.
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Temperature-induced phase separation of nonionic polyoxyethylated surfactant and application to extraction of metal thiocyanates.

Analytical chemistry

Okada T.
PMID: 19518042
Anal Chem. 1992 Sep;64(18):2138-42. doi: 10.1021/ac00042a019.

No abstract available.

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Okada T. Temperature-induced phase separation of nonionic polyoxyethylated surfactant and application to extraction of metal thiocyanates. Anal Chem. 1992;64(18):2138-42doi: 10.1021/ac00042a019.
Okada, T. (1992). Temperature-induced phase separation of nonionic polyoxyethylated surfactant and application to extraction of metal thiocyanates. Analytical chemistry, 64(18), 2138-42. https://doi.org/10.1021/ac00042a019
Okada, T. "Temperature-induced phase separation of nonionic polyoxyethylated surfactant and application to extraction of metal thiocyanates." Analytical chemistry vol. 64,18 (1992): 2138-42. doi: https://doi.org/10.1021/ac00042a019
Okada T. Temperature-induced phase separation of nonionic polyoxyethylated surfactant and application to extraction of metal thiocyanates. Anal Chem. 1992 Sep;64(18):2138-42. doi: 10.1021/ac00042a019. PMID: 19518042.
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Dihalo(imidazolium)sulfuranes: A Versatile Platform for the Synthesis of New Electrophilic Group-Transfer Reagents.

Journal of the American Chemical Society

Talavera G, Peña J, Alcarazo M.
PMID: 26132748
J Am Chem Soc. 2015 Jul 15;137(27):8704-7. doi: 10.1021/jacs.5b05287. Epub 2015 Jul 01.

The syntheses of imidazolium thiocyanates and imidazolium thioalkynes from dihalo(imidazolium) sulfuranes are reported and their reactivities as CN(+) and R-CC(+) synthons evaluated, respectively. The easy and scalable preparation of these electrophilic reagents, their operationally simple handling, broad substrate scope,...

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Talavera G, Peña J, Alcarazo M. Dihalo(imidazolium)sulfuranes: A Versatile Platform for the Synthesis of New Electrophilic Group-Transfer Reagents. J Am Chem Soc. 2015;137(27):8704-7doi: 10.1021/jacs.5b05287.
Talavera, G., Peña, J., & Alcarazo, M. (2015). Dihalo(imidazolium)sulfuranes: A Versatile Platform for the Synthesis of New Electrophilic Group-Transfer Reagents. Journal of the American Chemical Society, 137(27), 8704-7. https://doi.org/10.1021/jacs.5b05287
Talavera, Garazi, et al. "Dihalo(imidazolium)sulfuranes: A Versatile Platform for the Synthesis of New Electrophilic Group-Transfer Reagents." Journal of the American Chemical Society vol. 137,27 (2015): 8704-7. doi: https://doi.org/10.1021/jacs.5b05287
Talavera G, Peña J, Alcarazo M. Dihalo(imidazolium)sulfuranes: A Versatile Platform for the Synthesis of New Electrophilic Group-Transfer Reagents. J Am Chem Soc. 2015 Jul 15;137(27):8704-7. doi: 10.1021/jacs.5b05287. Epub 2015 Jul 01. PMID: 26132748.
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Showing 25 to 36 of 72 entries