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Showing 1 to 12 of 17 entries
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Latest development in the synthesis of ursodeoxycholic acid (UDCA): a critical review.

Beilstein journal of organic chemistry

Tonin F, Arends IWCE.
PMID: 29520309
Beilstein J Org Chem. 2018 Feb 20;14:470-483. doi: 10.3762/bjoc.14.33. eCollection 2018.

Ursodeoxycholic acid (UDCA) is a pharmaceutical ingredient widely used in clinics. As bile acid it solubilizes cholesterol gallstones and improves the liver function in case of cholestatic diseases. UDCA can be obtained from cholic acid (CA), which is the...

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Tonin F, Arends IWCE. Latest development in the synthesis of ursodeoxycholic acid (UDCA): a critical review. Beilstein J Org Chem. 2018;14:470-483doi: 10.3762/bjoc.14.33.
Tonin, F., & Arends, I. W. C. E. (2018). Latest development in the synthesis of ursodeoxycholic acid (UDCA): a critical review. Beilstein journal of organic chemistry, 14470-483. https://doi.org/10.3762/bjoc.14.33
Tonin, Fabio, and Arends, Isabel W C E. "Latest development in the synthesis of ursodeoxycholic acid (UDCA): a critical review." Beilstein journal of organic chemistry vol. 14 (2018): 470-483. doi: https://doi.org/10.3762/bjoc.14.33
Tonin F, Arends IWCE. Latest development in the synthesis of ursodeoxycholic acid (UDCA): a critical review. Beilstein J Org Chem. 2018 Feb 20;14:470-483. doi: 10.3762/bjoc.14.33. eCollection 2018. PMID: 29520309; PMCID: PMC5827811.
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Selenium-catalyzed oxidations with aqueous hydrogen peroxide. 2. Baeyer-Villiger reactions in homogeneous solution.

The Journal of organic chemistry

ten Brink GJ, Vis JM, Arends IW, Sheldon RA.
PMID: 11281784
J Org Chem. 2001 Apr 06;66(7):2429-33. doi: 10.1021/jo0057710.

Several diselenides were tested for catalytic activity in Baeyer-Villiger reactions with 60% aqueous hydrogen peroxide. Bis[3,5-bis(trifluoromethyl)phenyl] diselenide forms the corresponding 3,5-bis(trifluoromethyl)benzene seleninic acid in situ, which is a highly reactive and selective catalyst for the oxidation of carbonyl compounds...

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ten Brink GJ, Vis JM, Arends IW, et al. Selenium-catalyzed oxidations with aqueous hydrogen peroxide. 2. Baeyer-Villiger reactions in homogeneous solution. J Org Chem. 2001;66(7):2429-33doi: 10.1021/jo0057710.
ten Brink, G. J., Vis, J. M., Arends, I. W., & Sheldon, R. A. (2001). Selenium-catalyzed oxidations with aqueous hydrogen peroxide. 2. Baeyer-Villiger reactions in homogeneous solution. The Journal of organic chemistry, 66(7), 2429-33. https://doi.org/10.1021/jo0057710
ten Brink, G J, et al. "Selenium-catalyzed oxidations with aqueous hydrogen peroxide. 2. Baeyer-Villiger reactions in homogeneous solution." The Journal of organic chemistry vol. 66,7 (2001): 2429-33. doi: https://doi.org/10.1021/jo0057710
ten Brink GJ, Vis JM, Arends IW, Sheldon RA. Selenium-catalyzed oxidations with aqueous hydrogen peroxide. 2. Baeyer-Villiger reactions in homogeneous solution. J Org Chem. 2001 Apr 06;66(7):2429-33. doi: 10.1021/jo0057710. PMID: 11281784.
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The Baeyer-Villiger reaction: new developments toward greener procedures.

Chemical reviews

ten Brink GJ, Arends IW, Sheldon RA.
PMID: 15352787
Chem Rev. 2004 Sep;104(9):4105-24. doi: 10.1021/cr030011l.

No abstract available.

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ten Brink GJ, Arends IW, Sheldon RA. The Baeyer-Villiger reaction: new developments toward greener procedures. Chem Rev. 2004;104(9):4105-24doi: 10.1021/cr030011l.
ten Brink, G. J., Arends, I. W., & Sheldon, R. A. (2004). The Baeyer-Villiger reaction: new developments toward greener procedures. Chemical reviews, 104(9), 4105-24. https://doi.org/10.1021/cr030011l
ten Brink, G-J, et al. "The Baeyer-Villiger reaction: new developments toward greener procedures." Chemical reviews vol. 104,9 (2004): 4105-24. doi: https://doi.org/10.1021/cr030011l
ten Brink GJ, Arends IW, Sheldon RA. The Baeyer-Villiger reaction: new developments toward greener procedures. Chem Rev. 2004 Sep;104(9):4105-24. doi: 10.1021/cr030011l. PMID: 15352787.
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Efficient immobilisation of Rh-MonoPhos on the aluminosilicate AlTUD-1.

Chemical communications (Cambridge, England)

Simons C, Hanefeld U, Arends IW, Minnaard AJ, Maschmeyer T, Sheldon RA.
PMID: 15599428
Chem Commun (Camb). 2004 Dec 21;(24):2830-1. doi: 10.1039/b411506f. Epub 2004 Oct 26.

Rhodium-MonoPhos was successfully immobilised by ionic interactions on aluminosilicate AlTUD-1. The resulting new heterogeneous catalyst can be used in water and showed excellent enantioselectivity and activity in the asymmetric hydrogenation of methyl-2-acetamidoacrylate.

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Simons C, Hanefeld U, Arends IW, et al. Efficient immobilisation of Rh-MonoPhos on the aluminosilicate AlTUD-1. Chem Commun (Camb). 2004;(24):2830-1doi: 10.1039/b411506f.
Simons, C., Hanefeld, U., Arends, I. W., Minnaard, A. J., Maschmeyer, T., & Sheldon, R. A. (2004). Efficient immobilisation of Rh-MonoPhos on the aluminosilicate AlTUD-1. Chemical communications (Cambridge, England), (24), 2830-1. https://doi.org/10.1039/b411506f
Simons, Chretien, et al. "Efficient immobilisation of Rh-MonoPhos on the aluminosilicate AlTUD-1." Chemical communications (Cambridge, England) vol. ,24 (2004): 2830-1. doi: https://doi.org/10.1039/b411506f
Simons C, Hanefeld U, Arends IW, Minnaard AJ, Maschmeyer T, Sheldon RA. Efficient immobilisation of Rh-MonoPhos on the aluminosilicate AlTUD-1. Chem Commun (Camb). 2004 Dec 21;(24):2830-1. doi: 10.1039/b411506f. Epub 2004 Oct 26. PMID: 15599428.
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Photoenzymatic epoxidation of styrenes.

Chemical communications (Cambridge, England)

van Schie MMCH, Paul CE, Arends IWCE, Hollmann F.
PMID: 30666998
Chem Commun (Camb). 2019 Feb 05;55(12):1790-1792. doi: 10.1039/c8cc08149b.

Two-component-diffusible-flavomonooxygenases are versatile biocatalysts for selective epoxidation-, hydroxylation- or halogenation reactions. Their complicated molecular architecture can be simplified using photochemical regeneration of the catalytically active, reduced FADH2 prosthetic group. In this contribution we provide the proof-of-concept and characterization for...

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van Schie MMCH, Paul CE, Arends IWCE, et al. Photoenzymatic epoxidation of styrenes. Chem Commun (Camb). 2019;55(12):1790-1792doi: 10.1039/c8cc08149b.
van Schie, M. M. C. H., Paul, C. E., Arends, I. W. C. E., & Hollmann, F. (2019). Photoenzymatic epoxidation of styrenes. Chemical communications (Cambridge, England), 55(12), 1790-1792. https://doi.org/10.1039/c8cc08149b
van Schie, Morten M C H, et al. "Photoenzymatic epoxidation of styrenes." Chemical communications (Cambridge, England) vol. 55,12 (2019): 1790-1792. doi: https://doi.org/10.1039/c8cc08149b
van Schie MMCH, Paul CE, Arends IWCE, Hollmann F. Photoenzymatic epoxidation of styrenes. Chem Commun (Camb). 2019 Feb 05;55(12):1790-1792. doi: 10.1039/c8cc08149b. PMID: 30666998.
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Green, catalytic oxidation of alcohols in water.

Science (New York, N.Y.)

ten Brink GJ, Arends IW, Sheldon RA.
PMID: 10698735
Science. 2000 Mar 03;287(5458):1636-9. doi: 10.1126/science.287.5458.1636.

Alcohol oxidations are typically performed with stoichiometric reagents that generate heavy-metal waste and are usually run in chlorinated solvents. A water-soluble palladium(II) bathophenanthroline complex is a stable recyclable catalyst for the selective aerobic oxidation of a wide range of...

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ten Brink GJ, Arends IW, Sheldon RA. Green, catalytic oxidation of alcohols in water. Science. 2000;287(5458):1636-9doi: 10.1126/science.287.5458.1636.
ten Brink GJ, Arends, I. W., & Sheldon, R. A. (2000). Green, catalytic oxidation of alcohols in water. Science (New York, N.Y.), 287(5458), 1636-9. https://doi.org/10.1126/science.287.5458.1636
ten Brink GJ, et al. "Green, catalytic oxidation of alcohols in water." Science (New York, N.Y.) vol. 287,5458 (2000): 1636-9. doi: https://doi.org/10.1126/science.287.5458.1636
ten Brink GJ, Arends IW, Sheldon RA. Green, catalytic oxidation of alcohols in water. Science. 2000 Mar 03;287(5458):1636-9. doi: 10.1126/science.287.5458.1636. PMID: 10698735.
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Biocatalytic synthesis of the Green Note .

Beilstein journal of organic chemistry

van Schie MMCH, Pedroso de Almeida T, Laudadio G, Tieves F, Fernández-Fueyo E, Noël T, Arends IWCE, Hollmann F.
PMID: 29719567
Beilstein J Org Chem. 2018 Mar 26;14:697-703. doi: 10.3762/bjoc.14.58. eCollection 2018.

The biocatalytic preparation of

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van Schie MMCH, Pedroso de Almeida T, Laudadio G, et al. Biocatalytic synthesis of the Green Note . Beilstein J Org Chem. 2018;14:697-703doi: 10.3762/bjoc.14.58.
van Schie, M. M. C. H., Pedroso de Almeida, T., Laudadio, G., Tieves, F., Fernández-Fueyo, E., Noël, T., Arends, I. W. C. E., & Hollmann, F. (2018). Biocatalytic synthesis of the Green Note . Beilstein journal of organic chemistry, 14697-703. https://doi.org/10.3762/bjoc.14.58
van Schie, Morten M C H, et al. "Biocatalytic synthesis of the Green Note ." Beilstein journal of organic chemistry vol. 14 (2018): 697-703. doi: https://doi.org/10.3762/bjoc.14.58
van Schie MMCH, Pedroso de Almeida T, Laudadio G, Tieves F, Fernández-Fueyo E, Noël T, Arends IWCE, Hollmann F. Biocatalytic synthesis of the Green Note . Beilstein J Org Chem. 2018 Mar 26;14:697-703. doi: 10.3762/bjoc.14.58. eCollection 2018. PMID: 29719567; PMCID: PMC5905246.
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Highly efficient use of NaOCl in the Ru-catalysed oxidation of aliphatic ethers to esters.

Chemical communications (Cambridge, England)

Gonsalvi L, Arends IW, Sheldon RA.
PMID: 12120367
Chem Commun (Camb). 2002 Feb 07;(3):202-3. doi: 10.1039/b109390h.

The selectivity of alpha-oxidation of ethers to esters via Ru-NaOCl can be dramatically improved by pH control, at high substrate to catalyst ratios using a stoichiometric amount of hypochlorite in biphasic media at room temperature.

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Gonsalvi L, Arends IW, Sheldon RA. Highly efficient use of NaOCl in the Ru-catalysed oxidation of aliphatic ethers to esters. Chem Commun (Camb). 2002;(3):202-3doi: 10.1039/b109390h.
Gonsalvi, L., Arends, I. W., & Sheldon, R. A. (2002). Highly efficient use of NaOCl in the Ru-catalysed oxidation of aliphatic ethers to esters. Chemical communications (Cambridge, England), (3), 202-3. https://doi.org/10.1039/b109390h
Gonsalvi, Luca, et al. "Highly efficient use of NaOCl in the Ru-catalysed oxidation of aliphatic ethers to esters." Chemical communications (Cambridge, England) vol. ,3 (2002): 202-3. doi: https://doi.org/10.1039/b109390h
Gonsalvi L, Arends IW, Sheldon RA. Highly efficient use of NaOCl in the Ru-catalysed oxidation of aliphatic ethers to esters. Chem Commun (Camb). 2002 Feb 07;(3):202-3. doi: 10.1039/b109390h. PMID: 12120367.
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The surprisingly facile thermal dehalogenation of chlorinated aromatics by a hydroaromatic donor solvent. Tautomerization of chlorinated phenols and anilines.

The Journal of organic chemistry

Mulder P, Arends IW, Santoro D, Korth HG.
PMID: 12762723
J Org Chem. 2003 May 30;68(11):4247-57. doi: 10.1021/jo0265885.

Up to 600 K, chlorinated benzenes and naphthalenes are inert in a hydrogen atom donating solvent such as 9,10-dihydroanthracene. However, when a hydroxyl or amine group is attached to the 2 or 4 position relative to chlorine, a surprisingly...

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Mulder P, Arends IW, Santoro D, et al. The surprisingly facile thermal dehalogenation of chlorinated aromatics by a hydroaromatic donor solvent. Tautomerization of chlorinated phenols and anilines. J Org Chem. 2003;68(11):4247-57doi: 10.1021/jo0265885.
Mulder, P., Arends, I. W., Santoro, D., & Korth, H. G. (2003). The surprisingly facile thermal dehalogenation of chlorinated aromatics by a hydroaromatic donor solvent. Tautomerization of chlorinated phenols and anilines. The Journal of organic chemistry, 68(11), 4247-57. https://doi.org/10.1021/jo0265885
Mulder, Peter, et al. "The surprisingly facile thermal dehalogenation of chlorinated aromatics by a hydroaromatic donor solvent. Tautomerization of chlorinated phenols and anilines." The Journal of organic chemistry vol. 68,11 (2003): 4247-57. doi: https://doi.org/10.1021/jo0265885
Mulder P, Arends IW, Santoro D, Korth HG. The surprisingly facile thermal dehalogenation of chlorinated aromatics by a hydroaromatic donor solvent. Tautomerization of chlorinated phenols and anilines. J Org Chem. 2003 May 30;68(11):4247-57. doi: 10.1021/jo0265885. PMID: 12762723.
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Copper(II)-catalysed aerobic oxidation of primary alcohols to aldehydes.

Chemical communications (Cambridge, England)

Gamez P, Arends IW, Reedijk J, Sheldon RA.
PMID: 14587708
Chem Commun (Camb). 2003 Oct 07;(19):2414-5. doi: 10.1039/b308668b.

[CuBr2(2,2'-bipyridine)] catalyses the selective and very mild aerobic oxidation of primary alcohols to aldehydes in acetonitrile:water (2:1) in the presence of 2,2,6,6-tetramethylpiperidinyl-1-oxy (TEMPO) and a base as cocatalysts.

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Gamez P, Arends IW, Reedijk J, et al. Copper(II)-catalysed aerobic oxidation of primary alcohols to aldehydes. Chem Commun (Camb). 2003;(19):2414-5doi: 10.1039/b308668b.
Gamez, P., Arends, I. W., Reedijk, J., & Sheldon, R. A. (2003). Copper(II)-catalysed aerobic oxidation of primary alcohols to aldehydes. Chemical communications (Cambridge, England), (19), 2414-5. https://doi.org/10.1039/b308668b
Gamez, Patrick, et al. "Copper(II)-catalysed aerobic oxidation of primary alcohols to aldehydes." Chemical communications (Cambridge, England) vol. ,19 (2003): 2414-5. doi: https://doi.org/10.1039/b308668b
Gamez P, Arends IW, Reedijk J, Sheldon RA. Copper(II)-catalysed aerobic oxidation of primary alcohols to aldehydes. Chem Commun (Camb). 2003 Oct 07;(19):2414-5. doi: 10.1039/b308668b. PMID: 14587708.
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Identification of catalytically important residues of the carotenoid 1,2-hydratases from Rubrivivax gelatinosus and Thiocapsa roseopersicina.

Applied microbiology and biotechnology

Hiseni A, Otten LG, Arends IWCE.
PMID: 26481619
Appl Microbiol Biotechnol. 2016 Feb;100(3):1275-1284. doi: 10.1007/s00253-015-6998-y. Epub 2015 Oct 19.

Carotenoid 1,2-hydratases (CrtC) catalyze the selective addition of water to an isolated carbon-carbon double bond. Although their involvement in the carotenoid biosynthetic pathway is well understood, little is known about the mechanism by which these hydratases transform carotenoids such...

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Hiseni A, Otten LG, Arends IWCE. Identification of catalytically important residues of the carotenoid 1,2-hydratases from Rubrivivax gelatinosus and Thiocapsa roseopersicina. Appl Microbiol Biotechnol. 2015;100(3):1275-1284doi: 10.1007/s00253-015-6998-y.
Hiseni, A., Otten, L. G., & Arends, I. W. C. E. (2016). Identification of catalytically important residues of the carotenoid 1,2-hydratases from Rubrivivax gelatinosus and Thiocapsa roseopersicina. Applied microbiology and biotechnology, 100(3), 1275-1284. https://doi.org/10.1007/s00253-015-6998-y
Hiseni, Aida, et al. "Identification of catalytically important residues of the carotenoid 1,2-hydratases from Rubrivivax gelatinosus and Thiocapsa roseopersicina." Applied microbiology and biotechnology vol. 100,3 (2016): 1275-1284. doi: https://doi.org/10.1007/s00253-015-6998-y
Hiseni A, Otten LG, Arends IWCE. Identification of catalytically important residues of the carotenoid 1,2-hydratases from Rubrivivax gelatinosus and Thiocapsa roseopersicina. Appl Microbiol Biotechnol. 2016 Feb;100(3):1275-1284. doi: 10.1007/s00253-015-6998-y. Epub 2015 Oct 19. PMID: 26481619; PMCID: PMC4717167.
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Nanoparticles of lanthanide oxysulfate/oxysulfide for improved oxygen storage/release.

Dalton transactions (Cambridge, England : 2003)

Zhang W, Arends IW, Djanashvili K.
PMID: 27515224
Dalton Trans. 2016 Sep 28;45(36):14019-22. doi: 10.1039/c6dt01667g. Epub 2016 Aug 12.

Lanthanide oxysulfates have the ability to store and release large volumes of oxygen under oxidizing/reducing conditions, rendering them interesting as automotive catalysts. Herein we demonstrate a remarkable improvement of both processes by utilization of nanoparticles compared to the bulk...

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Zhang W, Arends IW, Djanashvili K. Nanoparticles of lanthanide oxysulfate/oxysulfide for improved oxygen storage/release. Dalton Trans. 2016;45(36):14019-22doi: 10.1039/c6dt01667g.
Zhang, W., Arends, I. W., & Djanashvili, K. (2016). Nanoparticles of lanthanide oxysulfate/oxysulfide for improved oxygen storage/release. Dalton transactions (Cambridge, England : 2003), 45(36), 14019-22. https://doi.org/10.1039/c6dt01667g
Zhang, Wuyuan, et al. "Nanoparticles of lanthanide oxysulfate/oxysulfide for improved oxygen storage/release." Dalton transactions (Cambridge, England : 2003) vol. 45,36 (2016): 14019-22. doi: https://doi.org/10.1039/c6dt01667g
Zhang W, Arends IW, Djanashvili K. Nanoparticles of lanthanide oxysulfate/oxysulfide for improved oxygen storage/release. Dalton Trans. 2016 Sep 28;45(36):14019-22. doi: 10.1039/c6dt01667g. Epub 2016 Aug 12. PMID: 27515224.
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Showing 1 to 12 of 17 entries